r. finmfi.‘fi - THIN Date 0-7639 lllllllllllllllllllllllll'llllllllllllllllllllllllllll 31293 01029 6576 This is to certify that the thesis entitled The RelationShip Between Exercise and Premenstrual Symptomatology presented by Elizabeth Ann Gale has been accepted towards fulfillment of the requirements for mSter degree in NUI'Sing {chel Schiffman Major professor 11-11-93 MS U is an Affirmative Action/Equal Opportunity Institution LlanAnv Michigan State University PLACE IN RETURN BOX to romovo this chockout from your rocord. TO AVOID FINES roturn on or botoro doto duo. DATE DUE DATE DUE DATE DUE MSU Io An Atflnnotivo Action/Equal Opportunity Institution «W ”311 THE RELATIONSHIP BETWEEN EXERCISE AND PREMENSTRUAL SYMPTOMATOLOGY BY Elizabeth Ann Gale A THESIS Submitted to Michigan State University in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE IN NURSING College of Nursing 1993 ABSTRACT THE RELATIONSHIP BETWEEN EXERCISE AND PREMENSTRUAL SYMPTOMOLOGY BY Elizabeth Ann Gale The purpose of this study was to investigate the physical, psychological and behavioral premenstrual symptoms most commonly self-reported by menstruating women between the ages of 30 to 46, who exercise, and to determine the relationship between exercise pattern and premenstrual symptomology. A retrospective survey design using Moos' MDQ and Stanley's Exercise Questionnaire was used. The sample of 37 women came from two sources: The "WOmen's Only'I 1992 race registration list and a private obstetric/gynecology office. The results of this study showed that women who exercise report mild to moderate premenstrual symptoms of weight gain, painful breasts, swelling, mood swings and irritability; and few symptoms of pain such as cramps, headaches and backaches. They also reported little premenstrual symptomology of negative affect, impaired There was no difference concentration and behavior change. in premenstrual symptomology among the different exercise groups. DEDICATION This thesis is dedicated to my husband, Geoff, for his support and technical assistance, and to my children Summer and Amber for their patience and understanding during the months in which this thesis was written. iii ACKNOWLEDGMENTS I would like to give thanks to my thesis committee: Rachel Schiffman, Brigid Warren, Jackie Wright, and Carol Rogers for their expertise and guidance for making this dream become a reality. I would also like to thank the thesis committee for their belief in me and their genuine concern and involvement in this project. Table of Contents Introduction.................................. ..... ... ....1 Research Question..... ......... . ..... . ..... . ............ ...2 Definition of Concepts...... ....... ..... ........ .. ......... 3 Premenstrual Syndrome Symptomatology. ..... . ............ :3 Exercise.. ......... .... ................................ .5 Review of the Literature ...... . .......................... ..8 Evaluation of the Literature..... .............. . ......... .11 Theoretical Framework.... ................ . ........ .. ..... .12 Methods.................. ................... . ....... .... .15 .. ..15 ...... ......OOOOOOOOOOOOOOOOOOO...O. Study Design.. Sample......... ....... ......... Field Procedures............................ ....... ....18 Protection of Human Subjects. ..... . ..... . ........... . .19 Operational Definitions...... ........ ........... ..... ..19 Instrumentation...................... .......... . .. ...23 Data Analysis...... ..... ...... ..... . ............... . ..26 ..... ...... .... ..27 AssumptiODSOOOOOOOOOOOOO Limitations of Study............ ...... .................28 Results................................ ............ .......28 Descriptive Findings of the Study Sample.. ............ .28 ......... ...28 Findings Related to Research Questions..... V Table of Contents 000...... Introduction............ Research Question........ ...... ............... ".3 Definition of Concepts. Premenstrual Syndrome Symptomatology.... Exercise..... ...... .. ..... . ...... . ............. .. ...... Review of the Literature ...... . ............................ 8 Evaluation of the Literature..... ......................... 11 ........... ......................12 Theoretical Framework.... Methods.......... ...... . Study Design.. ....... .......... .......... ........ .........1‘7 ......OOOIOOOOOOOOOOOOOO Sample...... 000000000018 Field Procedures............ ..... ......19 Protection of Human Subjects. ...... ....19 Operational Definitions.......... ....... Instrumentation.. .0 ....... Data Analysis. ...... .. ...... ...27 AssumptionSOOO...00.00.00... ........ oo0oooo00000oo000000000000000.28 Limitations of Study..... ooooo00o0o0oooooooo0oo0oooooooooooooo00000000.28 Results..... he Study Sample. ......... .....28 oooooo 000000.28 Descriptive Findings of t Findings Related to Research Questions.... Research Question 1.... ...... ....... ........ . ...... ....29 Prevalence of Premenstrual Symptomatology..............30 Severity of Premenstrual Symptoms........... ....... ....30 Research Question 2 .................................... 30 Exercise Characteristics...... ..... . ....... . ........... 32 Exercise Consistency..... ..... .. ...... . ............. ...32 Hypothesis Testing ....... . ....... . .......... .. ......... 36 Interpretation.......... ......... . ..... .. ................. 39 Implications for Nursing............ .................... . 46 Implication for Nursing Practice... .............. ......46 Recommendations for Future Research ................. ...49 Appendix A - Sample letters to potential study participants............................. ........ . ....... .51 Appendix B - University Committee On Research Involving Human Subjects (UCRIHS) approval .............. ..54 Appendix C - Instrument............ ............. ..........56 References.......... ..... ......... ............... .........63 vi Research Question 1..... ...... .. ............. . ...... ...29 Prevalence of Premenstrual Symptomatology ........ . ..... 30 Severity of Premenstrual Symptoms...... ..... .. ..... ....30 Research Question 2... ....... ...... ...... . ........ .....30 Exercise Characteristics....... ..... . .................. 32 Exercise Consistency ...... . ..... . ................ ......32 Hypothesis Testing.... ..... ........ ............. .......36 Interpretation.. ............... . .......... .. .............. 39 Implications for Nursing.......... ........................ 46 Implication for Nursing Practice............... ....... .46 Recommendations for Future Research...... ......... .....49 Appendix A - Sample letters to potential study participants....... ....... ........... ........... ..........51 Appendix B - University Committee On Research Involving Human Subjects (UCRIHS) approval.... ............ 54 Appendix C - Instrument.... ...... .. ...... . ..... . .......... 56 References...... ......... .. ...... ............ ........... ..63 w List of Tables Table 1 MDQ Scales Derived From Menstrual, Premenstrual, Intermenstrual, and Worst Cycle Factor Analysis Table 2 Demographic Characteristics Table 3 Per Cent of Premenstrual Symptomatology Reported Table 4 Per Cent of Severity of Most Prevalent Premenstrual Symptoms Table 5 Exercise Characteristics Table 6 Exercise Consistency Table 7 Means, Standard Deviations, and Range for Each Phase of the Most Recent Cycle Table 8 Analysis of Variance for Differences in Mean Total Score of the MDQ Subscales and the Different Exercise Groups vfi 22 29 31 32 33 34 36 37 iyvy ‘i i .. .AV. All, :2 . . = Z, .1. was ““I‘II’II‘IIIII‘IIIIIIIIIIIIII 31293 01029 6576 This is to certify that the thesis entitled 'Ihe Relationship Between Exercise and Premenstrual Symptomatology presented by Elizabeth Ann Gale has been accepted towards fulfillment of the requirements for Master degree in Nursing {achelw Schiffman Major professor Date 11-11-93 0-7639 MS U is an Affirmative Action/Equal Opportunity Institution ___—..__ . 77,. . 1 if, if LIBRARY Michigan State University PLACE IN RETURN BOX to remove this checkout from your record. TO AVOID FINES return on or before date due. DATE DUE DATE DUE DATE DUE MAY172001 3'30 5 o 4 MSU ie An Affirmative Action/Equal Opportunity Inetitution mans-9.1 THE RELATIONSHIP BETWEEN EXERCISE AND PREMENSTRUAL SYMPTOMATOLOGY BY Elizabeth Ann Gale A THESIS Submitted to Michigan State University in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE IN NURSING College of Nursing 1993 ABSTRACT THE RELATIONSHIP BETWEEN EXERCISE AND PREMENSTRUAL SYMPTOMOLOGY BY Elizabeth Ann Gale The purpose of this study was to investigate the physical, psychological and behavioral premenstrual symptoms most commonly self-reported by menstruating women between the ages of 30 to 46, who exercise, and to determine the relationship between exercise pattern and premenstrual symptomology. A retrospective survey design using Meos' MDQ and Stanley's Exercise Questionnaire was used. The sample of 37 women came from two sources: The "WOmen's Only“ 1992 race registration list and a private obstetric/gynecology office. The results of this study showed that women who exercise report mild to moderate premenstrual symptoms of 'weight gain, painful breasts, swelling, mood swings and irritability; and few symptoms of pain such as cramps, headaches and backaches. They also reported little premenstrual symptomology of negative affect, impaired concentration and behavior change. There was no difference in premenstrual symptomology among the different exercise groups. DEDICATION This thesis is dedicated to my husband, Geoff, for his support and technical assistance, and to my children Summer and Amber for their patience and understanding during the months in which this thesis was written. iii ACKNOWLEDGMENTS I would like to give thanks to my thesis committee: Rachel Schiffman, Brigid Warren, Jackie Wright, and Carol Rogers for their expertise and guidance for making this dream become a reality. I would also like to thank the thesis committee for their belief in me and their genuine concern and involvement in this project. Research Question 1.............. ...................... 29 Prevalence of Premenstrual Symptomatology..............30 Severity of Premenstrual Symptoms....... ........... ....30 Research Question 2.... .............................. ..30 Exercise Characteristics ............................... 32 Exercise Consistency. ............ .. ................ ....32 Hypothesis Testing. ..... ........... .................... 36 Interpretation......... ................................... 39 Implications for Nursing.......... .................... ....46 Implication for Nursing Practice... .................. ..46 Recommendations for Future Research...... .............. 49 Appendix A - Sample letters to potential study participants.................................. ...... ......51 Appendix B - University Committee On Research Involving Human Subjects (UCRIHS) approval. ............... 54 Appendix C - Instrument..................... ..... . ...... ..56 References................................ .............. ..63 w List of Tables Table 1 MDQ Scales Derived From Menstrual, Premenstrual, Intermenstrual, and Worst Cycle Factor Analysis Table 2 Demographic Characteristics Table 3 Per Cent of Premenstrual Symptomatology Reported Table 4 Per Cent of Severity of Most Prevalent Premenstrual Symptoms Table 5 Exercise Characteristics Table 6 Exercise Consistency Table 7 Means, Standard Deviations, and Range for Each Phase of the Most Recent Cycle Table 8 Analysis of Variance for Differences in Mean Total Score of the MDQ Subscales and the Different Exercise Groups vii 22 29 31 32 33 34 36 37 List of Figures Figure 1 Exercise and PMS Pattern Manifestation Appraisal Model 16 Figure 2 PMS Symptom Profile of Women Who Exercise 44 VW Introduction Premenstrual syndrome is a constellation of physical, psychological and/or behavioral symptoms arising from an observable pattern related to the menstrual cycle. Women who suffer from PMS symptomatology may experience emotional and physical discomfort during the premenstrual phase of - their menstrual cycle. PMS is one of the most common complaints of childbearing women with an estimated 2% to 85% of women having at one time or another experienced at least one of the PMS symptoms (Johnson, McChesney, & Bean, 1988; Wilhelm-Hass, 1984; Woods, Most, & Dery, 1982). Women may experience PMS symptomatology at any age during their reproductive years. However, there is evidence that PMS symptomatology increases in severity with age and that women over age 30 seek treatment for PMS at higher rates than women under 30 years of age (Hsia & Long, 1990; Johnson, McChesney, & Bean, 1988; Kirkpatrick, Brewer, & Stocks, 1990). The four most widely accepted theories of PMS are progesterone deficiency, excess of prostaglandins, deficiency of prostaglandins, and excess of estrogen (Hsia & Long, 1990). The etiology of PMS remains an enigma; therefore, clinicians prescribe treatment based on the woman's symptoms of PMS. The emergence of the beta-endorphin 2 deficiency theory as an etiology for PMS has generated interest in the use of exercise as a treatment modality for PMS symptomatology. Current literature suggests that exercise plays an important role in the management of PMS by reducing stress and increasing beta-endorphin levels in women who suffer from PMS symptomatology (Carr et al., 1981). There is no literature that examines the pattern of exercise in women and how this pattern might be associated- with PMS symptomatology. Clinical Nurse Specialists in the primary care setting will have clients present with PMS symptomatology and will need a basis on which to make therapeutic decisions. The purpose of this study was twofold: (1) to examine PMS symptomatology in a sample of women who exercise, and (2) to determine the relationship between the pattern of exercise in women and the pattern of PMS symptomatology. Research Questions The research questions addressed in this study were: 1.) What physical, psychological, or behavioral premenstrual symptoms are most commonly self-reported by a sample of menstruating women, 30 to 46 years of age, who exercise? 2.) Is there a relationship between the pattern of exercise in menstruating women 30 to 46 years of age and the severity of self-reported premenstrual symptoms? 3 Definition of Concepts Premenstrua 8 nd ome S to ato o Dalton (1984) succinctly describes premenstrual syndrome as "the recurrence of symptoms in the premenstruum with absence of symptoms in the postmenstruum" (p.7). She further elaborates that recurrence of symptoms means a repetition of symptoms for a minimum of three consecutive cycles and that the severity of the symptoms may vary from cycle to cycle. For example, one premenstrual cycle may be characterized by a headache relieved with analgesics. The next cycle may be characterized by an excruciating migraine with visual disturbances that causes loss of functioning (Dalton, 1984). Dalton (1984) explains that the absence of symptoms in the postmenstruum requires a phase of a minimum of seven days free from all symptoms. Premenstrual syndrome has been defined by Magos and Studd (1986) as the distressing physical, psychologic, and behavioral symptoms, not caused by organic disease, which regularly occur during some phase of the menstrual/ovarian cycle and which disappear or significantly regress during the remainder of the cycle. Rubinow and Roy-Byrne (1984) define PMS as "the cyclic occurrence of symptoms that are of sufficient severity to interfere with some aspects of life and appear with a consistent and predictable relationship to menses" (p. 114). The American Psychiatric Association labels PMS as Periluteal Phase Dysphoric Disorder. Periluteal Phase 4 Dysphoric Disorder is described as a pattern of clinically significant emotional and behavioral symptoms that occur during the last week of the luteal phase and remit within a few days after the onset of the follicular phase (DMS-III, 1987). Diagnostic criteria include the following: (a) symptoms that correspond to the two phases of the menstrual cycle, (b) a disturbance that seriously interferes with work or with social activities and relationships, and (c) a disturbance that is not merely an exacerbation of the symptoms of another disorder, such as Major Depression, Panic Disorder, or Personality Disorder (DMS-III, 1987). It is very clear that the above definitions all share a common theme of PMS symptoms occurring in a cycle with a pattern. The above definitions of PMS stress that there is a symptom period as well as a distinct symptom-free period related to the menstrual cycle. Sveinsdotter and Reame (1991) examined the symptom characteristics and patterns of menstrual cycles in seven healthy women who suffered from PMS. The PMS group in their study displayed a pattern type of increasing severity across the menstrual cycle. According to Burkhart (1991), symptoms associated with premenstrual syndrome can be categorized into physical symptoms and psychological/behavioral symptoms. The common physical symptoms associated with PMS are: abdominal bloating, headaches, breast enlargement and tenderness, constipation, edema of extremities, acne, and craving for sweets or salty foods. The psychological/behavioral 5 symptoms associated with PMS are: anxiety, mood swings, depression, irritability, lethargy, crying spells, hostility, low morale, and sleep disorders (Burkhart, 1991). Woods, Most, and Dery (1982) found that symptoms with a prevalence greater than 30 per cent included: weight gain, headache, skin disorders, cramps, anxiety, backache, fatigue, painful breast, irritability, mood swings, depression, and tension. For the purpose of this study PMS symptomatology was defined as a cluster of symptoms related to the menses which is manifested by a pattern of physical, psychological, and/or behavioral symptoms. Exercise Exercise is defined as physical activity that is planned, structured, repetitive, and purposeful (McArdel, Katch, & Hatch, 1991). Physical activity is defined as any body movement produced by muscles that results in increased energy expenditure (McArdel et al., 1991). The terms "exercise“ and "physical activity" have been used interchangeably in the literature. There is a distinct difference between the two. According to Caspersen, Powell, and Christenson (1985) exercise is a subcategory of physical activity. They concede that exercise contains the following components: (a) bodily movement via skeletal muscles, (b) results in energy expenditure, (c) energy expenditure (kilo- calories) varies continuously from low to high, (d) very positively correlated with physical fitness, (e) is planned, structured, and repetitive, and (f) an objective is to 6 improve or maintain physical fitness. Physical activity contains only the first four components of exercise (Casperen et al., 1985). Fair, Rosenaur, & Thurston (1979) define physical exercise as an action or an activity involving either physical and/or mental exertion. Fair et a1. (1979) define aerobic or endurance exercise as exercise which promotes cardiac conditioning such as running, jogging, biking, swimming and walking. Allan (1985) also describes aerobic- exercise as exercise that promotes cardiopulmonary endurance or fitness. She further elaborates by stating they are rhythmic, repetitive exercises that create a demand for increasingly larger amounts of oxygen by using large muscle groups. The three components to an exercise program are: (a) frequency, (b) intensity, and (c) duration. Frequency refers to how many days per week the exercise is performed (Allan, 1985). Studies have shown that fitness can be attained and maintained on a frequency of three times per week (Pollack, 1971; Fox, Naughton, & Gorman, 1972; Merriman, 1978). Intensity refers to target heart rate. Target heart rate is exercising at a level of 70 to 85 per cent of maximal heart rate (Allan, 1985). Duration is considered the specific length of time an individual exercises for each exercise session (Allan, 1985). 7 Consistency is another component of exercise that was addressed in this study. Consistency was defined in this study as the regularity, constancy, and uniformity of the exercise program one is engaged in. Consistency is the unaltered state of an exercise program. In other words, the exercise program is not altered or changed due to normal life circumstances such as time constraints. The American College of Sports Medicine (1990) recommends the following guidelines for developing and maintaining cardiorespiratory fitness, body composition, and muscular strength and endurance in the healthy adult: (a) frequency of training: 3-5 days per week, (b) intensity of training: 60%-90% of maximum heart rate, (c) duration of training: 20-60 minutes of continuous aerobic activity. The benefits of aerobic training include prevention of heart disease, weight control, higher tolerance to fatigue, and a reduction in tension, depression, and mood changes (Canty, 1934). The above definitions imply that exercise contains an element of planned activity that is repetitious and ongoing. An exercise pattern is developed from this rhythmic, repetitive activity. For the purpose of this study exercise pattern was defined as the frequency, duration, and consistency of a planned, rhythmic, repetitive activity involving large muscle groups. 8 Review of the Literature There is a paucity of literature on studies on PMS and exercise. Timonen and Procope' (1971) analyzed the effect of physical exercise on PMS by sending out questionnaires to 1,000 female students. Of a thousand questionnaires distributed 748 were returned. Timomen and Procope' (1971) concluded that girls who exercised regularly showed fewer PMS symptoms than their less active counterparts. This was a poorly written, retrospective study with confusing tables and lacking in a clear definition of PMS, with no validity and reliability of instruments. Israel, Sutton, and O'Brien (1985) studied the effects of aerobic training on primary dysmenorrhea in 36 college- aged females suffering from primary dysmenorrhea. Eighteen subjects were randomly assigned to a training program consisting of a 30-minute continuous walk/jog program three days a week at an intensity of 70-85% of heart rate range for twelve weeks. Eighteen subjects were randomly selected as a control and were asked not to exercise during the twelve week period. Primary dysmenorrhea symptomatology was measured using the Moos Menstrual Distress Questionnaire (MDQ). The results of this study showed that the training group had lower mean MDQ scores than the control group. The direct cause for the decline in the MDQ scores in the training group was not established in this study. The authors speculate that the release and rise in beta- endorphin in the training group could explain the perception 9 of less discomfort in dysmenorrhea (Israel et al., 1985). This was a prospective, controlled study investigating the effects of a training program on subjects who suffered from primary dysmenorrhea. It is unclear if the variable being studied was dysmenorrhea or premenstrual syndrome. Prior, Vigna, Sciarretta, Alojado, and Schulzer (1987) found an association between exercise and PMS symptomatology. Prior et a1. (1987) studied twenty-one women with a mean age of 33.4 years. Eight sedentary women volunteered to begin a 6-month training program. Seven women runners who were training for a marathon (26.2 mile road race) volunteered to record training and menstrual cycle data over six months. Six nontraining women served as the control group. All subjects monitored body temperature, weight, and their exercise program. There was no change in body weight, body mass or menstrual cycle interval in the subjects. The training and marathon groups experienced significant decrease in several premenstrual symptoms at six months. The control group experienced no change in premenstrual symptoms. This was a prospective, controlled study in which PMS was clearly the outcome variable. The major flaw in this study is the small sample size and one must use caution when interpreting results. Stanley (1985) conducted a survey on the relationship between exercise and PMS for a thesis project on 116 women, ranging in age from 18 to 53 years. The subjects were recruited from three different sources: (a) a PMS clinic, 10 (b) a lecture on PMS, and (c) a PMS conference. All subjects believed that they had PMS and were seeking treatment for PMS or information on PMS. The survey instrument included an exercise questionnaire and a health questionnaire, which contained a modified version of the Moos Menstrual Distress Questionnaire. Stanley (1985) found that there was a significant inverse relationship between exercise and PMS. Stanley showed that women who exercise report few PMS symptoms. Limitations of this study were:- (a) it was unclear whether the exercise questionnaire was tested for validity and reliability, (b) all subjects were volunteers, (c) there was no control group, and (d) the sample was comprised of women from one of the highest socioeconomic areas in the United States (Stanley, 1985). A homogeneous group of college aged women was used in both the Timonen and Procope' study (1971) and the Israel et al. (1985) study. Prior et al. (1987) and Stanley (1985) used a more heterogenous group for their sample. Prior et al. (1987) used a sample of women with a mean age of 33.4 while Stanley used a sample of women between the ages of 18 to 53 years old. The Israel et al. (1985) and Prior et al. (1987) studies were similar in that each was a prospective, controlled study in which exercise was the independent variable. A retrospective survey questionnaire was used in both the Timonen and Procope' study (1971) and the Stanley (1985) study. However, Stanley's study was much better ll documented than Timonen and Procope's with the variables being clearly defined. Although, the literature fails to address the antithesis that exercise increases PMS symptomatology, considerable attention has been given to exercise induced menstrual disorders. Researchers have found that menstrual dysfunction does exist in distance runners. The most common exercise induced menstrual disorders are oligomenorrhea and amenorrhea (Boyden, Pamenter, Stanforth, Rotkins, & Wilmore, 1983; Bullen, Skrinar, Beitins, VonMering, Turnbull, & McArthur, 1985; Dale, Gerlach, & Wilhite, 1979). If exercise can have such a profound effect on the menstrual cycle one needs to wonder what effect it has on PMS symptomatology. t ‘ atu Of the three studies found in the literature on exercise and its effects on PMS only Prior et al. (1987) clearly define PMS. Timonen and Procope' (1971) make no attempt to define PMS in their study and Israel et al. (1985) label PMS as dysmenorrhea. Researchers need to critically define PMS and remain consistent with the definition and diagnostic criteria for PMS (Logue & Moos, 1986) in future studies. Timonen and Procope' (1971) conducted a cross- sectional study on exercise and PMS that was poorly documented (Prior et al., 1987). Israel at al. (1985) were the first to attempt a controlled trial of exercise and PMS, 12 but failed to clearly discern PMS as the outcome variable. Prior et al. (1987) successfully completed a controlled study of the relationship of exercise and PMS showing that women who exercise report less PMS symptoms than women who do not exercise. Although, Prior et al. (1987) conducted a well documented, controlled study more research is indicated to make a definitive statement that exercise decreases PMS symptomatology. To date there are no studies that disprove that exercise alleviates PMS (Prior et al., 1987). - The studies cited do not distinguish women who experience mild symptoms of PMS to women who suffer severe, incapacitating symptoms of PMS. Researchers need to delineate mild symptoms of PMS from severe symptoms and show how exercise pattern affects the various degrees of PMS symptomatology. Researchers should also question whether strenuous exercise exacerbates or mitigates severe PMS symptomatology. Theoretical Framework The theoretical foundation used for this study is Rogers' Science of Unitary Human Beings. Rogers (1986) defined unitary human beings as "irreducible, four- dimensional energy fields identified by pattern and manifesting characteristics that are different from those of the parts and cannot be predicted from knowledge of the parts” (p.5). Unitary human beings are open systems. Unitary human beings are exemplified as energy fields in open process with environmental energy fields (Smith, 1986). 13 Energy fields have pattern (Fawcett, 1989). This continuous, changing human and environmental fields is depicted as a wave pattern (Smith, 1986). Pattern distinguishes human energy fields from their environmental energy fields. Patterns are abstractions that are observable through nonrepeating rhythms that are constantly changing. Manifestations of patterns are analogous to the wave pattern of the Great Lakes. The waves of the great body of waters are rhythmic and continuous but the wave pattern is constantly changing. There is continuous variation in the waves due to shift in the winds, interruption by water craft and change in the tide. Human energy field patterns are observable through manifestations of pattern such as amount of exercise and perceptions of PMS symptomatology. The practice of nursing mainly involves assessment and identification of the manifestations of patterns that emerge from the mutual person and environmental energy field process and deliberative patterning through a nurse and person mutual process (Lutjens, 1990). The nurse and client participate in deliberative mutual patterning; the nurse facilitates the client's actualization of potentials for health and well being (Cowling, 1989). Pattern manifestation appraisal enables the nurse to assess recurring life themes and issues through sensory information, thoughts, feelings, perceptions, experiences, imagination, memory, and expressions of her/his clients l4 (Cowling, 1989). Pattern manifestation appraisal centers on "identifying manifestations of human and environmental fields that relate to current health events" (Barrett, 1988, p. 50). Roger's unitary pattern-based practice model was used in this study for identifying manifesting patterns of PMS symptoms such as pain, bloating, breast enlargement, anxiety, and irritability in a sample of women who exercise. A pattern profile of PMS symptoms in exercising women was'. developed incorporating properties, features, and qualities derived from the pattern information. These properties include an assessment of the exercise pattern of these women. The author also investigated how exercise pattern affects PMS pattern symptomatology. Three distinct exercise patterns were identified through pattern manifestation appraisal. These patterns demonstrated the rhythmicity and continuum of human energy fields. Pattern group A consisted of infrequent, and/or inconsistent exercise behavior, of short duration depicted in Figure 1 as a very sporadic wave pattern with much variation in the shape and size of the peaks. Pattern group B consisted of exercise behavior that is of moderate frequency, consistency and duration depicted in Figure 1 as an irregular wave pattern with some variation in the shape and size of the peaks. Pattern group C consisted of exercise behavior that was frequent, consistent and of extended duration depicted in Figure 1 as a very constant 15 wave pattern with uniformity in the shape and size of the peaks. The model shown in Figure 1 shows the pattern of the three different groups and how exercise pattern is related to perceived amount of PMS symptoms (PMS symptom profile). The more consistent the exercise pattern the less PMS symptomatology. The nurse fits in this model by assessing and identifying exercise pattern manifestation and perceived PMS symptomatology manifestation in menstruating women. - Methods Study Design A retrospective, survey questionnaire was used to address the research questions. In a retrospective study, the sample is questioned or interviewed after the fact. A retrospective study is a practical and efficient method of collecting data in a relatively short period and is used often in nursing research (Polit & Hungler, 1991). This was a non-experimental, ex post facto, correlational study. The researcher did not control for the independent variable, pattern of exercise. The researcher did not manipulate the pattern of exercise in the study sample. The researcher did not randomly assign individuals to different exercise pattern groups. The dependent variable in this study was the perceived amount of PMS symptoms. £91121: A nonprobability convenience sample of 37 women between the age of 30 and 46 was used for this study. The criteria 16 EXERCISE PATTERN LOW - FREQUENCY CONSISTENCY M p M S DURATION EXERCISE PATTERN MODERATE - FREQUENCY cons I STENCY I PM E, DURATION EXERCISE PATTERN HIGH - FREQUENCY CONSISTENCY PMS DURATION PMS : PMS Symptom Profl Ie Figure 1 EXERCISE AND PMS PATTERN MANIFESTATION APPRAISAL MODEL 17 for inclusion in this study were women: (a) between the ages of 30 to 46, (b) currently not on progesterone therapy, oral contraceptives or psychotropic agents, (c) who had two consecutive menstrual periods 20 to 40 days apart at the time of completing the questionnaires, and (d) who currently reported exercising. Women on progesterone therapy, oral contraceptives or psychotropic agents were excluded from this study because these agents may be used for the treatment of PMS - symptomatology. Oral contraceptives and progesterone also alter the menstrual cycle and may confound premenstrual symptomatology. The normal menstrual cycle is 28 days in duration, but cycles may range from 20 to 40 days and still be considered normal (Ensign, Rowe, & Kowalski, 1988). Women who reported any deviation from the average normal cycle were excluded from this study because abnormally long or short periods may confound premenstrual symptomatology. The sample was obtained from two different sources: (a) the 1992 "Women's Only" Race register list, and (b) a large obstetric/gynecology group practice in Lansing, Michigan. "Women's Only" is a two day annual event held in Flint, Michigan which includes a women's health fair, fashion show and dinner, and an 8 kilometer run, 8 kilometer competitive walk, 5 kilometer run, and 5 kilometer fitness walk. The researcher selected 100 names from the "Women's Only" 1992 register list for the sample. This was done by selecting every fourth label from the computerized printout until 25 18 labels were selected from each of the four race categories totalling 100 names. Of the 100 questionnaires sent, 46 were returned for a 46% response rate. Of the 46 returned questionnaires, 8 were excluded due to current birth control use; 4 were excluded due to improper completion of the MDQ questionnaire; and 2 were excluded because the subjects reported that they did not exercise. This resulted in 32 usable questionnaires from the "Women's Only" register list. The researcher obtained 8 completed questionnaires from the office site. Of the 8 questionnaires obtained from this site, 2 were excluded due to current birth control use and 1 because she reported she did not exercise. This resulted in 5 usable questionnaires from the office site. W The questionnaires were mailed with instructions to the "Women's Only" participants selected for the study. A stamped, return envelope was included to facilitate response. The researcher mailed the questionnaires with written instruction (Appendix A). Subjects from the private office site were selected on a voluntary basis. The office nurse distributed the questionnaires during a one month period to women from 30 to 46 years of age as they came into the clinic for their health care needs. Those wishing to fill out the questionnaire did so while waiting for their appointment. There was a deposit box available in the waiting area forthe completed questionnaires. The response rate was low for this sample. l9 ontegtiog of Human Subjects Protection of human subjects in regard to confidentiality was insured by anonymity. No one including the investigator was able to associate responses from the questionnaire with individual subjects. This was done by instructing subjects not to write their name on the questionnaires. No attempt was made to identify returned questionnaires with names on the "Women's Only" register list. Subjects were instructed that by returning the completed questionnaire they were giving consent. The private office clients were also assured anonymity by instructing subjects not to write their name on the questionnaire. The deposit box was placed in a safe area free from intrusion. Office personnel did not tamper with the box. The box contained one envelope size slot and was tightly secured with packaging tape. Subjects were instructed that by completing the questionnaire and depositing it in the box they were giving consent. This project was approved by the University Committee on Research Involving Human Subjects (Appendix B). 0 er a De ' itio Exercise pattern was operationalized according to self- reported frequency, duration, and consistency of exercise. The subjects were divided into three groups according to their pattern of exercise. Exercise pattern was determined by responses to questions 1, 2, 5, 6, 7, and 8 of the Exercise Questionnaire (refer to questionnaire in Appendix 20 C). Question 1 of the Exercise Questionnaire addressees the frequency of exercise. Question 2 of the Exercise Questionnaire addresses the duration of exercise. Questions 5, 6, 7, and 8 address the consistency of exercise. Questions 1 and 2 were scored using the following rules. In question 1 answer (a) received a score of 0, answer (b) received a score of 1, answer (c) received a score of 2, and answer (d) received a score of 3. Question one of the Exercise Questionnaire measured the frequency of exercise. In question 2 answer (a) received a score of 1, answer (b) received a score of 2, and answer (c) received a score of 3. Question 2 of the Exercise Questionnaire measured the duration of exercise. In questions 5 through 8 answer (a), (c), and (d) received a 0 and answer (b) received a 1. The scores from questions 5 through 8 were totalled. The total score of questions 5 through 8 measured consistency of exercise. Each respondent had three scores, one representing their exercise frequency, the second representing their exercise duration, and a third representing their exercise consistency. These scores were then combined for a final score. A final score of 2-5 represented Pattern group A consisting of low frequency, low duration, and inconsistent exercise. A final score of 6-7 represented Pattern group 8 consisting of moderate frequency, moderate duration and moderately consistent exercise. A final score of 8-10 21 represented Pattern group C consisting of high frequency, long duration and very consistent exercise. The physical, psychological, and behavioral components of premenstrual syndrome symptomatology was operationalized by using six of the eight subscales of the Moos' Menstrual Distress Questionnaire as presented in Table 1. The subscales of Pain, Water Retention, and Autonomic Reactions reflected the physical or somatic symptoms. The subscale of Negative Affect reflected the psychological symptoms. - Impaired Concentration and Behavior Change reflected the behavioral symptoms. The subscales of Arousal and Control were eliminated from this study because neither reflects the physical, psychological, or behavioral symptoms generally associated with premenstrual symptoms. The Arousal subscale taps the positive reactions that some investigators have linked with the menstrual cycle (Moos, 1985). The Control subscale is composed of items that are rarely reported as being related to the menstrual cycle (Moos, 1985). The complete MDQ contains 47 items that are individually scored on a Lickert scale ranging from 0 to 4, with 0 being no experience of symptoms; with 1 meaning symptoms are present, mild; with 2 meaning symptoms are present, moderate; with 3 meaning symptoms are present, strong; and with 4 meaning symptoms are present, severe. The items were then added for a total score for each subscale. For example, the water retention scale included the items weight gain, skin blemish or disorder, painful or 22 Table 1 Egg Sgales Derived from Menstrual, Premenstrual, t ‘411‘1.t ,- 810 WS ..e. --. , ‘ - t0 ‘_ a, S. 1 Pain 5 Impaired Concentration Muscle Stiffness Insomnia Headache Forgetfulness Cramps Confusion Backache Poor judgement Fatigue Difficulty General aches and concentration pains Distractible Minor motor 2 Water Retention coordination Weight gain Skin blemish/disorder Painful or tender breasts 3 Autonomic Reactions Dizziness, faintness Cold sweats Nausea, vomiting 6 Behavior Change Poor school or work performance Take naps, stay in bed Stay at home Avoid social activities Deceased efficiency Hot flashes 4 Negative Affect Loneliness Anxiety Mood swings Crying Irritability Tension Feeling sad or blue Restlessness blots. From WWW (p.3) by R. H. Moos, 1991, Los Angeles: Western Psychological Services. Copyright 1991 by Western Psychological Services. Reprinted by permission. 23 tender breasts, and swelling. A raw score for water retention was tabulated by adding the scores of the 4 items defining the scale for each cycle phase. The raw score was then divided by the number of items to arrive at a mean score. The same method of scoring was done on the other 5 subscales of the MDQ. For this study prevalence was defined as symptoms reported by over half of the women. Severity was determined by the raw score of each of the 47 items of the MDQ reported during the four days before the menstrual cycle. A score of 1 or 2 received a value of 1 meaning mild to moderate severity. A score of 3 or 4 received a value of 2 meaning severe to disabling. These values were then entered into SPSS which then calculated the frequency for each value and the percent for each value for all 47 items. Instrumentation The investigator used two instruments to measure the concepts: one was an adaptation of Carol Stanley's Exercise Questionnaire to determine exercise pattern and the other was Moos' Menstrual Distress Questionnaire to determine premenstrual symptomatology. The Exercise Questionnaire (Appendix C) is an eight item forced answer questionnaire adapted from Carol Stanley (1985) to measure frequency, duration, and consistency of exercise. The original questionnaire contained 11 items. Four items were deleted because they were dealing with past exercise pattern and 24 intention to exercise. The remaining item responses were altered semantically to enable a more accurate measurement of exercise pattern and consistency. Question 8 regarding exercise habits during menses was added to give a more accurate measurement of exercise pattern and consistency over the entire menstrual cycle. The Moos' Menstrual Distress Questionnaire (MDQ) Form C (Appendix D) was used to measure PMS symptomatology. The MDQ was developed over 20 years ago and has been used extensively in the area of PMS research (Facchinetti, Martignoni, Petraglia, Sances, Nappi, & Genazzani, 1987; Shelley, & Anderson, 1986; & Woods et al., 1982). Moos (1985) tested the MDQ on a sample of 839 women to arrive at the present factor structure with eight subscales. All of the eight subscales of the MDQ are positively correlated. Negative Affect and Impaired Concentration were the most highly correlated at 0.68. Pain and Negative Affect, Pain and Behavior Change, and Pain and Impaired Concentration were the next most highly correlated pairs at 0.59, 0.58, and 0.57 respectively. Negative Affect and Arousal were among the least correlated at .18. The factor analysis performed by Moos suggested a moderate to high degree of construct validity of the instrument. Factor analysis performed on subsets of the MDQ scales provided further support of moderate to high construct validity of the MDQ. Woods, Most, and Dery (1982) in their sample of 179 women found internal consistencies, as 25 estimated by Cronbach's Alpha, to be between 0.64 and 0.88for these four scales: Pain, Water Retention, Negative Affect, and Impaired Concentration. The questionnaire was examined for reliability of the eight subscales for the initial sample of 839 subjects (Moos, 1985). In the initial sample the sub-scale internal consistencies, as measured by Kuder-Richardson Formula 20, varied between 0.89 for the Negative Affect scale, and 0.53 for the Control scale. Piccolo (1982) obtained similar - results for reliability in a sample of 156 college students. Internal consistency reliabilities for the present study's sample of 37 women between the ages of 30 and 46 as estimated by Cronbach's Alpha were: Pain 0.65, Water Retention 0.75, Autonomic Reactions 0.32, Negative Affect 0.87, Impaired Concentration 0.67, and Behavior Change 0.53. The internal consistencies for the subscales Pain, Water Retention, Negative Affect, and Impaired Concentration were moderate suggesting that the items on the scale are measuring the same characteristic for this sample of women. The subscale Autonomic Reactions had a very low alpha coefficient which indicated that the items on this scale were not measuring the same characteristic for this sample of women. The alpha was increased moderately to 0.58 by deleting item 16 (hot flashes) from the questionnaire. The subscale Behavior Change had a moderately low alpha coefficient which was not significantly increased by deleting any of the items suggesting moderately low 26 reliability. The alpha coefficient for Impaired Concentration was increased from 0.67 to 0.78 by deleting item 23 (insomnia) giving a moderate to high alpha. There is no standard for what an acceptable reliability coefficient should be (Polit & Hungler, 1991). However, coefficients in the vicinity of 0.70 is considered sufficient when making group-level comparisons (Polit & Hungler, 1991). The alpha's derived from the sample in the present study have an overall lower reliability coefficient score than those obtained from previous studies. There is evidence of moderate to high inter-cycle stability (reliability) of women's menstrual cycle symptom reports (Moos, 1985). That is, women tend to report similar symptoms from one menstrual cycle to another (Moos, 1985). Moos (1985) also found that a "woman's retrospective reports of her symptoms are not affected by the menstrual cycle phase she is in when completing the MDQ" (p. 9). Rapkin, Chang, & Reading (1988) compared a retrospective PMS questionnaire to a daily PMS diary in 17 women by having the women complete the daily diary, as well as the retrospective study. Their study suggest that women reliably report cyclical variation in PMS symptomatology when assessed by retrospective report. W A. Means and standard deviations were calculated for the demographic variable of age. Frequencies and percents 27 were calculated for the variables of marital status and educational level to describe the sample. B. The first research question (What physical, psychological, or behavioral premenstrual symptoms are most commonly self-reported by a sample of menstruating women, 30 to 46 years of age, who exercise?) was addressed by obtaining frequencies and percentages of 35 items representing the physical, psychological, and/or behavioral symptoms of premenstrual symptomatology to determine the " prevalence of premenstrual symptoms. C. The second research question (Is there a relationship between exercise pattern in menstruating women 30 to 46 years of age and the severity of self-reported premenstrual syndrome symptoms?) was addressed by using one- way ANOVA's to test the significant differences among the three different exercise groups with the 6 MDQ subscales. Mean scores and standard deviations for each of the 6 subscales of the MDQ was obtained to determine the self- reported severity of the physical, psychological, an/or behavioral cluster of PMS symptoms. 5993132312135 A. People are basically honest and therefore, the women answered the questionnaire honestly. 8. Women were able to accurately recall their premenstrual symptomatology. 28 I. 'l !' E 5! I A. The researcher was unable to control for factors which may influence PMS symptomatology such as the following: (a) women who exercise may also practice other self-care behaviors such as maintaining a diet low in caffeine, refined sugar, salt, red meat, and fat, (b) women who exercise may maintain lower body fat composition than their nonexercising counterparts, and (c) the psychosocial make-up of women who exercise may be different than the - psychosocial make-up of women who do not exercise (different personality types). B. All subjects were volunteers. Women who experience frequent, moderate to severe premenstrual symptoms may have been more likely to participate in this study because of their personal interest in the subject. Therefore, the prevalence rates and self-reported severity rates may be high. C. Since this was a convenience sample of women, results may not be generalizable to other women. Results De ' ’ F S m le The mean age of participants was 38.92 (s.d. 3.70) years. Most participants were married, well educated, and all 37 were white (Table 2). u st 5 The following describes the findings for the research questions addressed by the study. 29 W: What physical, psychological, and/or behavioral premenstrual symptoms are most commonly self-reported by a sample of menstruating women, 30 to 46 years of age, who exercise? Table 2 Demographic Characteristics (N = 37) - Characteristic Frequency Per cent Karim Single 4 10.8 Married 29 78.4 Divorced 1 2.7 Widowed O 0.0 Living with partner 2 5.4 Missing 1 2.7 ve Some high school 0 0.0 High school graduate 7 18.9 Trade or business school 1 2.7 Some college 8 21.6 College graduate 8 21.6 Post-graduate 13 35.1 The first research question was addressed by obtaining frequencies and percentages of 35 selected items from the MDQ that measures the presence of the physical, psychological, and behavioral symptoms associated with premenstrual symptomatology. 30 o e t S t o The percentage of women reporting the 35 selected premenstrual symptoms is given in Table 3. The 35 selected items assess for the presence of the physical, psychological, and behavioral symptoms associated with premenstrual symptomatology. The six most prevalent premenstrual symptoms, reported by more than half the women for this sample, included weight gain, swelling, mood swings, irritability, fatigue, and painful breasts. Severity of Premegstrual Symptoms Of these symptoms, most women reported their symptoms to be mild to moderate in severity (Table 4). Three of the six most prevalent premenstrual symptoms for this sample fell into the Water Retention subscale (weight gain, swelling, and painful breasts). One (fatigue) was in the Pain subscale. Two were in the Negative AffeCt subscale (mood swings and irritability). Symptoms that fall into the Autonomic Reactions, Impaired Concentration, and Behavioral Change subscales had a low prevalence rate with low severity. Overall, most women reported mild to moderate symptoms of PMS symptomatology. W Is there a relationship between the pattern of exercise in menstruating women 30 to 46 years of age and the severity of self-reported premenstrual symptoms? 31 Table 3 2g; gen; 0: Premenstrual Symptomatology Reported (N = 371 Symptom Per cent Weight gain 73.0 Swelling 64.9 Mood swings 62.2 Irritability 62.2 Fatigue 59.5 Painful or tender breasts 59.5 Tension 48.6 Skin blemish 45.9 Anxiety 40.5 Feeling sad or blue 37.8 Backache 29.7 Headache 27.0 General aches and pains 27.0 Cramps 24.3 Take naps, or stay in bed 24.3 Crying 18.9 Restlessness 18.9 Loneliness 18.9 Muscle stiffness 13.5 Forgetfulness 13.5 Decrease efficiency 13.5 Poor work or school performance 10.8 Insomnia 10.8 Stay at home 10.8 Distractible 10.8 Poor judgment 08.1 Dizziness 08.1 Poor motor coordination 05.4 Difficulty concentrating 05.4 Confusion 05.4 Avoid social activities 05.4 Cold sweats 05.4 Hot flashes 02.7 02.7 02.7 Nausea\vomiting Minor accidents 32 Table 4 Pe C Seve 't O ost P evalent P eme strual EXEQEQEE Per cent Per cent Symptom N M/M S/D Weight gain 27 74.1 25.9 Swelling 24 83.3 16.7 Mood swings 23 65.2 34.8 Irritability 23 69.6 30.4 Fatigue 22 72.7 27.3 Painful breasts 22 68.2 31.8 N = Number of women who reported symptom M/M Mild, moderate S/D Severe, disabling Exercise Characteristics As can be seen in Table 5 most women from this sample exercised at least 3 times a week for a duration of 40 minutes or longer. The two most common types of exercises reported were running and walking. Most women reported exercising for more than 4 years. These findings suggest that the women from this sample exercise on a regular basis and have established a moderate to high level exercise pattern. s'st Most women from this sample reported changing their exercise schedule if their life became cluttered with unexpected events or if they felt poorly physically. Most did not change their exercise schedule if they felt poorly emotionally or during their menses. described in Table 6. Table 5 33 WIN = 371 Exercise consistency is Characteristic Frequency Per cent E c' e enc Once a month to twice a week 3 to 4 times a week 5 or mere times a week 'se u ' n Less than 20 minutes 20 to 40 minutes 40 minutes or more W Walking Running Swimming Aerobics Cycling Other W Less than 1 month Less than 6 months Less than 1 year 1 to 2 years 2 to 3 years 3 to 4 years More than 4 years 15 15 13 24 12 H OOCDOQ idh'etnaaazo 18.9 40.5 40.5 The sample was divided into three groups according to their exercise pattern as described in the operational definition section. The low level group consisted of 6 34 women, the moderate level exercise group consisted of 15 women, and the high level exercise group consisted of 16 women. Table 6 s te = 7 Characteristic Frequency Per cent Life flecopes Cluttered with unexpected events Change schedule 22 59.5 No schedule change 15 40.5 Fe “ca Change schedule 28 75.7 No schedule change 9 24.3 e na Change schedule 13 35.1 No schedule change 24 64.9 e es Change schedule 4 10.8 No schedule change 33 89.2 The means, standard deviations, and ranges were calculated for the total scores of each of the six MDQ subscales for the three different phases of the menstrual cycle to measure the spread or variability of self-reported premenstrual symptoms. The means for each subscale was much lower in the intermenstrual phase than the premenstrual and menstrual phases. This means that women from this sample experience few, if any, symptoms during the intermenstrual 35 phase which was consistent with the definition of premenstrual symptomatology. The standard deviations shown in Table 7 point to considerable interindividual variation in reports of menstrual cycle symptoms for this sample. For example, a woman who was 2 standard deviations above the mean would obtain a score of 10.95 on the Pain scale in the premenstrual phase. This score represents an average report of "present, moderate" on all six Pain items or, more - likely, a report of "present, strong" or "present, severe" on two or three items and little or no experience of the other symptoms (Moos, 1985). The ranges also showed considerable variation in reports of menstrual cycle symptoms. Histograms of the data showed that the sample was grossly skewed. Histograms of the Pain, Autonomic Reactions, Negative Affect, Impaired Concentration, and Behavior Change subscales showed the data to have an asymmetrical shape with positive skewness and outliers. A histogram of the Water Retention subscale showed a symmetrical shape without outliers. The histograms reveal that this data is not tightly clustered around the means. There is variation in the data sets with the exception of the Water Retention subscale. Interpretation of the means, standard deviations, and ranges of the subscales was done with caution because of the wide distribution of the data sets. 36 Table 7 ‘11: 21!: o D- - 01‘ one 'a 0e - g 2 ’1o 9 the HOSE Becepp Cycle in = 371 Premenstrual Menstrual Intermenstrual Sub Total Total Total Scale Mean SD Range Mean SD Range Mean SD Range Pain 3.51 3.72 0-14 3.95 3.73 0-16 0.89 1.37 0-06 WR 4.65 3.55 0-11 3.27 3.26 0-11 0.43 0.80 0-03 Auto 0.38 0.98 0-24 0.30 0.85 0-03 0.16 0.60 0-03 NA 4.86 5.13 0-18 4.68 5.13 0-18 1.73 3.78 0-17 IC 0.78 1.75 0-09 0.78 1.53 0-07 0.38 0.85 0-04 SC 0.86 1.25 0-05 1.05 2.58 0-15 0.24 0.55 0-02 Subscale Possible range for each subscale Pain = WR - 0 Pain - Pain 0 Auto 2 O - l6 WR = Water Retention Auto 8 Autonomic Reactions NA 8 Negative NA = 0 32 IC 8 Impaired Concentration IC = 0 32 BC 2 0 - 20 BC - Behavioral Change Hypetheeie Testing One-way analysis of variance was used to compare the three different exercise groups and mean total scores on the six subscales of the MDQ: Pain, Water Retention, Autonomic Reactions, Negative Affect, Impaired Concentration, and Behavioral Change. On the basis of this analysis (see table 8), there was a difference in the mean scores of the Pain subscale among the different exercise groups. The Tukey method of post hoc comparisons was used to test which groups differed in perceived amount of pain in the premenstrual phase of the menstrual cycle. The low exercise group showed 37 higher mean total scores than the moderate and high exercise groups in the Pain subscale. Table 8 Anaiysie Of Variance For Differences In Mean Total Score them 9: giving them ppaise fem thei; exercise efforts. 0; sca ' e 'se rou 8 Scale N M so F-ratio df F Proa- Pain Low exercise 6 8.67 4.50 10.50 2,36 0 .0003 Moderate exercise 15 2.00 1.90 High exercise 16 3.19 3.30 We '0 Low exercise 6 6.00 3.90 1.14 2,36 0.3303 Moderate exercise 15 3.67 3.60 High exercise 16 5.13 3.40 hgpohemie heactiohs Low exercise 6 0.00 0.00 1.03 2,36 0.3668 Moderate exercise 15 0.13 0.51 High exercise 16 0.50 1.21 N ect Low exercise 6 6.33 6.71 0.06 2,36 0.9358 Moderate exercise 15 6.33 7.20 High exercise 16 5.36 5.34 Impaipeg echeentpatioh Low exercise 6 0.83 1.32 0.61 2,36 0.4463 Moderate exercise 15 0.20 0.41 High exercise 16 0.90 2.15 Be av n e Low exercise 6 1.00 2.00 0.61 2,36 0.5468 Moderate exercise 15 0.53 0.83 High exercise 16 1.00 1.26 There were no differences in the mean total scores of the Water Retention, Autonomic Reactions, Negative Affect, Impaired Concentration, and Behavioral Change subscales among the different exercise groups. The null hypothesis 38 that there is no relationship between exercise pattern and PMS symptomatology cannot be rejected based on this analysis. Exercise pattern of women between the ages of 30 and 46 had no effect on the perceived amount of premenstrual symptomatology. Table 8 shows that women who are in the low exercise group have higher mean scores in the Pain scale than women who are in the moderate and high exercise groups. Women in the moderate exercise group have lower mean scores in the Water Retention and Behavior Change scale than the‘. women in the low and high exercise groups, but this finding was not statistically significant. There were no differences in the total mean scores among the three groups in the Autonomic Reactions, Negative Affect, or Impaired Concentration scales. These women essentially reported very few symptoms in the Autonomic Reactions, Negative Affect, and Impaired Concentration subscales regardless of their exercise pattern. Cochran's C was used to test for homogeneity of variance between the groups. There was no difference in variation between groups in the Pain, Negative Affect, and Water Retention subscales. However, Cochran's C was significant between groups in the Autonomic Reactions, Impaired Concentration, and Behavior Change. Even though ANOVA is a robust test results of this study must be interpreted with caution because the assumption that the variances in all groups must be equal was not met and the population did not have a normal distribution. 39 Interpretation The sample in the present study was composed of white, highly educated, married women. Most of the sample (32) was from taken from the " Womens' Only" register list. Women who participate in the "Womens' Only" road race were white, educated, and married. This phenomenon could be a result of many factors. Married women may have more social support than single women such as spouse running or walking with Married women may experience fewer barriers and have better access to exercise. Married women may have husbands that accept child care duties while the wife exercises. Married women may have husbands who contribute to household duties providing more time for exercise. Married women may enjoy a higher socioeconomic status providing more opportunities for exercise. Women who are educated may be more cognizant of the benefits of exercise than women who are not educated. Running and walking may be considered activities for educated whites and blacks or less educated women may feel uncomfortable participating in such activities. The most prevalent self-reported premenstrual symptoms of women 30 to 46 years of age who exercise were weight gain, fatigue, swelling, tender breasts, mood swings, and irritability. The literature shows that the symptoms most commonly associated with premenstrual syndrome in the general population are fatigue, swelling, breast tenderness, skin disorders, mood swings, anxiety, depression, irritability, lethargy, crying spells, low 40 morale, and sleep disorders (Johnson, McChesney, & Bean, 1988; Wilhelm-Mass, 1984; Woods, Most, & Dery, 1982). The prevalence of premenstrual symptomatology in this sample of women 30 to 46 years of age who exercise is similar but not identical to that of other populations studied to date. Woods et a1. (1982) found, in their sample of 179 women between the ages of 18 and 35, a prevalence of weight gain to be 48 per cent, headache to be 38 per cent, swelling to be 46 per cent, and tension to be 43 per cent. Lee and - Rittenhouse (1991) found in their sample of 594 women between the ages of 21 to 50 symptoms to have a prevalence rate of greater than 30 per cent were cramps, weight gain, swelling, headache, anxiety, irritability, tension, backache, fatigue, painful breasts, and mood swings. This sample of women reported little premenstrual symptomatology of pain such as cramps, headaches, and backaches. They also reported little premenstrual symptomatology of negative affect, impaired concentration, and behavior change such as depression, insomnia, and decreased efficiency, respectfully. It is of interest that this sample of women reported a higher prevalence rate of symptoms in the Water Retention scale than other study samples. One could speculate that women who exercise are concerned with their weight and are very sensitive to water retention symptoms. Most of the previous studies were done on younger women. This is the first study done on a sample of 41 exclusively older women (30 to 46 years of age) who exercise. Other studies did not exclude women who were on birth control pills, hormone therapy, diuretics, antidepressants, or sedatives. Women who were on birth control pills, hormone therapy, diuretics, antidepressants, and sedatives were excluded from this study. Taking into consideration that older women generally report more premenstrual symptoms than younger women and that certain medications positively affect PMS symptoms, this sample of- women show low to moderate PMS symptomatology. The women of this sample clearly showed a pattern of exercise and this pattern was rhythmic and continuous but constantly changing. Women from this study showed a moderate amount of consistency in their exercise habits. Women tended to change their exercise pattern when unexpected life events occurred and when they were feeling poorly physically. It stands to reason that one would not exercise when feeling poorly physically. In this sample of women their exercise schedule changed in response to unexpected life events. It can be extrapolated that exercise is important to this sample of women but does not take absolute priority in their lives. This sample of women did not change their exercise schedule when feeling poorly emotionally. Perhaps this sample of women use exercise as a form of mental health therapy. Most women of this sample reported not changing their exercise behavior during their 42 menses. This sample of women may experience low menstrual discomfort or exercise may take precedence over comfort. This study showed that women who exercise report low severity of premenstrual symptoms. The women of this study reported mild to moderate premenstrual symptoms of fatigue, weight gain, swelling, tender breasts, mood swings, and irritability. There was no difference in premenstrual symptomatology among the different exercise pattern groups. This finding suggests that exercise in general can have a - positive effect on the perceived amount of premenstrual symptomatology in women. The low exercise group showed significantly higher mean scores on the Pain subscale than the moderate and high exercise groups. This could be explained by the beta- endorphin theory. Increased blood levels of beta-endorphins have been found after exercise (Hsia & Long, 1990). Increased circulating beta-endorphins has been associated with analgesia and euphoria (Hsia & Long, 1990). Women who exercise at a moderate to high exercise level may have more circulating beta-endorphins than their low exercise cohorts and have natural analgesia decreasing their pain symptoms. The human energy field pattern of this sample of women is observable through manifestations of exercise pattern such as frequency, duration, and consistency of exercise and through manifestations of premenstrual symptomatology. The original model presented earlier was not supported by the 43 results of this study. However, Rogers' unitary pattern- based practice model was used to develop a PMS symptomatology profile for women over 30 who exercise. Weight gain, fatigue, painful breasts, swelling, mood swings, irritability, and tension in the largest box depict the most frequently self-reported premenstrual symptoms in this sample of women. Skin disorders, anxiety, and feeling sad in the medium-size box depict the second most frequently self-reported premenstrual symptoms. Backache, cramps, - taking naps, and headaches in the small box depict the third most frequently self-reported premenstrual symptoms. The revised model in Figure 2 depicts the premenstrual symptomatology pattern profile of women who exercise. The results of this study show that exercise pattern has little effect on how women report premenstrual symptoms. However, women in the moderate exercise group reported less symptoms in the Behavior Change and Water Retention subscales of the MDQ. The majority of the women (80%) inthis study had a fairly consistent exercise pattern. The results of this study also show that women between the age of 30 to 46 years of age, who exercise experience low severity of premenstrual symptoms. Methodological problems for this study include a small sample size, lack of a control group, data collection was done through a mailed questionnaire, and the researcher needed to rely on retrospective recall for reports of PMS symptomatology. A larger sample size may have reduced the 44 WEIGHT GAIN SWELLING PAINFUL BREASTS FATIGUE IRRITABILITY MOOD SWING TENSION I I I M / I SKIN DISORDERS _/\\__3/\.__5/\__/\_._/ ANXIETY FEELING SAD I BACKACHE I ’ \ I CRAMPS TAKE NAPS HEADACHE Figure 2 PMS SYMPTOM PROFILE OF WOMEN WHO EXERCISE 45 effect of extreme scores in the subscales and eliminated outliers giving the sample a more symmetrical shape. A control group of "no exercisers" could have been used to compare the effect exercise has on premenstrual symptomatology. Another disadvantage of this study is that the researcher had to rely on mailed questionnaires for data collection. Mailed questionnaires commonly have a poor response rate. Although, the response rate for this study- was high with 46% of the women returning the questionnaire. However, some of the questionnaires could not be used due to the respondents failure to complete the questionnaire accurately. A major shortcoming of a mailed questionnaire is the inability to provide clarification of questions when needed. Having to rely on retrospective recall may have had a limited effect on the recollection of the presence or absence of premenstrual symptoms and may have resulted in an overestimation of symptom severity. A data analysis problem for this study is that the assumptions of analysis of variance were not met. The first assumption that the groups must be a random sample from a normal population was violated. The data was grossly skewed not meeting the criteria of normalcy. The assumption that in the population, the variances in all groups must be equal was also violated for one-way analysis. 46 Implications For Nursing Nursing implications derived from the findings of this study are in the areas of nursing practice and future nursing research using Rogers' unitary pattern-based practice model as the conceptual framework. I . . . e The Family Clinical Nurse Specialist (FCNS) provides primary health care to individuals and families on the continuum of the life span. It is common knowledge that women are the most likely age and gender group to enter the health care delivery system. Women usually enter the health care system seeking contraception upon becoming sexually active. It is very typical for women to stay in the health delivery system for health maintenance visits related to contraception and prenatal care. One of the primary roles of the FCNS in clinical practice is to provide a health maintenance history and physical promoting health and wellness for individuals. The FCNS provides these services to women in a variety of settings including family practice offices, family planning centers, OB/GYN offices, college campuses, and women's clinics. This study of a sample of women 30 to 46 years of age who exercise showed a prevalence rate of premenstrual symptomatology of up to 70% but with low severity. The most commonly reported premenstrual symptoms were weight gain, fatigue, swelling, tender breasts, mood swings, and 47 irritability. The FCNS may provide anticipatory guidance for women who are approaching 30 by talking to them about the common symptoms related to the premenstruum or counsel women who are suffering from premenstrual symptoms. The FCNS can provide PMS counseling, education, and treatment focusing on the most prevalent premenstrual symptoms. Most women reported symptoms from the Water Retention and Pain subscales. The FCNS needs to be knowledgeable in the use of diuretics and prostaglandin inhibitors in the treatment of- premenstrual symptoms. Many women will not seek help for their premenstrual symptoms with the belief that it is "normal" to have these cyclic episodes of pain and discomfort. The first step the FCNS takes in the management of premenstrual symptomatology is to recognize that a premenstrual related problem exists. If the FCNS determines that a premenstrual problem exists he/she than needs to assess for the severity of symptoms. This could be done by administering the MDQ or another reliable instrument that measures premenstrual symptomatology and severity. The FCNS functions as an assessor by systematically collecting subjective and objective data and formulating premenstrual symptomatology diagnoses or problems related to premenstrual syndrome. It is very likely that FCNS's will provide health services in a variety of settings to women who present with premenstrual symptomatology. These settings could include family planning and health services to low-income and 48 minority women in low cost clinics. The FCNS can be creative in the development and prescription of an exercise program for this population group by networking with area churches and neighborhood clubs. The FCNS could act as a facilitator and help organize church and neighborhood walking or aerobic programs for this population group. Based on the prevalence rate of women experiencing premenstrual symptoms it is imperative that the nurse in advanced practice assess for premenstrual symptomatology in women. Rogers' unitary pattern-based model is a useful tool for the assessment of premenstrual symptoms. Rogers' pattern manifestation appraisal model provides a systematic approach in the identification of premenstrual symptomatology pattern. The nurse in advanced practice can develop a pattern profile of clients who present with PMS symptomatology. The etiology of premenstrual symptomatology remains unclear. The clinician managing premenstrual symptomatology has many treatment options available such as hormone therapy, diuretics, psychotropic therapy and stress management techniques. Based on this study the nurse in advanced practice may prescribe a moderate exercise program as part of the treatment plan of clients who present with premenstrual symptoms of pain. The results of this study show that women who exercise experience the common symptoms of PMS, but report low severity of symptoms. This study also shows that exercise does not worsen or exacerbate 49 premenstrual symptoms and may even reduce symptom severity in the Pain subscale. Exercise is a self-care behavior that has many benefits such as cardiovascular fitness, weight control, and stress management and should be included in the PMS treatment plan if not otherwise contraindicated. W The sample in the present study consisted mainly of women who participated in the "Women's Only" race who were from the ages of 30 to 46 years old. These women were - white, well-educated, and married. A study including a variety of subjects from different racial and ethnic backgrounds, lower educational levels, a wider age range and cultural differences would produce conclusions applicable to a broader population. More experimental studies that include a control group and groups assigned to specific exercise levels are needed to support the hypothesis that there is an inverse relationship between PMS and exercise. Most of the studies done on PMS and exercise used retrospective recall questionnaires; more studies need to be done using prospective questionnaires or asking women to keep daily diaries of symptoms related to their menses. This study raises more questions than answers in regard to the relationship between exercise pattern and PMS symptomatology. Further research is needed to explore why women who exercise report most of their PMS symptoms in the Water Retention subscale. Further research 50 investigatingthis relationship is necessary in order to draw any definitive conclusions. The data from this study suggest that women who exercise report mild to moderate premenstrual symptoms. These data are limited to women from southeast Michigan, who participated in the Women's Only race who are between the ages of 30 to 46 years. Further study is necessary to ascertain whether these symptoms are characteristic of childbearing women of all ages and women who participate in other forms of exercise. APPENDICES Appendix A Sample letters to potential study participants. 52 To: Lansing OB/GYN Clients From: Elizabeth Gale RN Date: February 16, 1993 I am a Registered Nurse pursuing a Master's Degree in Nursing at Michigan State University. I am doing research on exercise pattern and the menstrual cycle for my thesis project. The results of the study will be helpful to nurses providing care to childbearing women. Will you please take time to complete the enclosed questionnaire while you are.- waiting for your appointment? The questionnaire takes about ten minutes to complete. No attempt will be made to identify you in any way. Please do not write your name on the questionnaire or envelope. Participation in this study is voluntary and you are under no obligation to participate. If you do not wish to participate in this study your care at Lansing OB/GYN Associates will not be affected in any way. You indicate your voluntary agreement to participate by completing and depositing the questionnaire into the box labelled "Study". A written summary of the results of this study will be available in this office in the Fall of 1993. If you have any questions concerning your health as a result of completing this questionnaire please consult your health care provider. Thank you very much for your assistance. 53 To: "Women's Only" Participants From: Elizabeth Gale RN Date: February 16, 1993 I am a Registered Nurse pursuing a Master's Degree in Nursing at Michigan State University. I am doing research on exercise pattern and the menstrual cycle for my thesis project. The results of the study will be helpful to nurses providing care to childbearing women. Will you please take time to complete the enclosed questionnaire and return it in the stamped, self-addressed envelope by March 1, 1993. The questionnaire takes about ten minutes to complete. No attempt will be made to identify you in any way. Please do not write your name on the questionnaire or envelope. Participation in this study is voluntary and you are under no obligation to participate. You indicate your voluntary agreement to participate by completing and returning this questionnaire. A written summary of the results of the study will be available at the 1993 "Women's Only" race at one of the information tables. If you have any questions concerning your health as a result of completing this questionnaire please consult your health care provider. Thank you very much for your assistance. Appendix B University Committee on Research Involving Human Subjects (UCRIHS) approval. 55 MICHIGAN STATE UNIVERSITY OFFICE OF VICE PRESIDENT FOR RESEARCH AND DEAN OF THE GRADUATE SCHOOL EAST LANSING 0 MICHIGAN 0 488244046 February 10. 1993 TO: Ms. Elizabeth Gale 1225 Clearview Drive Flushing. MI 48433 RE: IRB #: 93-027 TITLE: THE RELATIONSHIP BETWEEN EXERCISE PATTERN AND PREMENSTRUAL SYMPTOMATOLOGY REVISION REQUESTED: N/A CATEGORY: l-C - APPROVAL DATE: 02/09/1993 The University Committee on Research Involving Human Subjects' (UCRIHS) review of this project is complete. I am pleased to advnse that the rights and welfare of the human subiects appear to be adequately protected and methods to obtain informed consent are appropnate. Therefore. the UCRIHS approved this project including any revision listed above. UCRIHS approval is valid for one calendar year. beginning with the approval date shown above. Investigators planning to continue a project beyond one year must seek updated certification. Request for renewed approval must be accompanied by all four of the following mandatory assurances. l. The human subjects protocol is the same as in previous studies. 2. There have been no ill effects suffered by the subjects due to their participation in the study. 3. There have been no complaints by the subjects or their representatives related to their participation in the study. 4. There has not been a change in the research environment nor new information which would indicate greater risk to human subjects than that assumed when the protocol was initially reviewed and approved. There is a maximum of four such expedited renewals possible. Investigators wishing to continue a project beyond that time need to submit it again for complete rewew. UCRIHS must review any changes in procedures involving human subjects. prior to initiation of the change. Investigators must notify UCRIHS promptly of any problems (unexpected side effects. complaints. etc.) involvmg human subjects during the course of the work. If we can be of any future help, please do not hesitate to contact us at (517) 355-2180 or FAX (517) 336-1171. avid E. Wright. Ph.D. UCRII-IS Chair Sincerely. DEW:pjm cc: Dr. Rachel Schiffman MSU is an Affirmative Action/Equal Opportunity Insulation Appendix c Instruments 57 Exercise Questionnaire Today's date: Age: Race:___White ___Black Asian or Pacific Islander Hispanic ___Other, specify Marital Status: (circle one) a. single b. married c. divorced d. widowed e. living with partner Educational level: a. some high school b. high school graduate c. trade school or business school d. some college e. college graduate f. post-graduate work at a college or university Have you taken any of the following medications within the last 6 months? (You may indicate more than one answer). a. sedative b. antidepressant c. water pill (diuretic) d. birth control pill e. progesterone f. Norplant g. estrogen The following questionnaire is designed to determine the amount of exercise that you do. Please answer each question only once. Please circle your response or, where appropriate, write your response in the space provided. 1. On the average, how often do you exercise? a. never (if you answer never please go to the Menstrual Distress Questionnaire) b. once a month to twice a week c. 3 to 4 times a week d. 5 or more times a week 2. When you do your exercise how much time on the average do you spend at each session? a. less than 20 minutes b. 20 to 40 minutes c. 40 minutes or more 58 What type of exercise do you participate in most frequently? ONE ANSWER ONLY. a. walking b. running c. swimming d. aerobics e. cycling f. other How long have you been exercising? a. less than 3 months b. less than 6 months c. less than 1 year d. 1 to 2 years e. 2 to 3 years f. 3 to 4 years - g. more than 4 years If your life becomes cluttered with unexpected events, do you... a. exercise more than normal b. do not change your exercise schedule c. exercise less than you normally would d. not exercise at all If you are feeling poorly physically, do you... a. exercise more than normal b. do not change your exercise schedule c. exercise less than you normally would d. not exercise at all If you are feeling poorly emotionally, do you... a. exercise more than normal b. do not change your exercise schedule c. exercise less than you normally would d. not exercise at all When you are on your "period" do you... a. exercise more than normal b. do not change your exercise schedule c. exercise less than you normally would d. not exercise at all 45. 46. 47. 62 Most recent flow (A) Blind spots, fuzzy vision. ........... Poor motor coordination...... ...... Increased appetite...... Four days before (B) Remain- der of cycle (C) 61 1 2 3 Most Four Remain- recent days der of flow before cycle (A) (B) (C) 22. RestlessneSSOOOOOOOOO... 23. Insomnia........... 24. Poor school or work performance............ 25. Affectionate.. .......... 26. Feelings of suffocation. ........... 27. Forgetfulness........... 28. Take naps, stay in bedOOOOOOOOOOOOOOOOO... 29. Orderliness. ......... ... 30. Chest pains ............. 31. Confusion..... ..... ..... 32. Poor judgment........... 33. Stay at home............ 34. Excitement....... ....... 35. Ringing in the ears ..... 36. Difficulty concentrating ........... 37. Avoid social activities...... ..... ... 38. Feelings of well- being.................. 39. Heart pounding.......... 4o. Distractible...... ..... . 41. Decreased efficiency.... — _ _ * 42. Bursts of energy, activity................ 43. Numbness, tingling...... 44. Minor accidents......... 6O Descriptive Categories: - No experience of symptom - Present, mild O 1 2 - Present, moderate 3 - Present, strong 4 - Present, severe 1 2 3 Most Four Remain- recent days der of flow before cycle (A) (B) (C) 1. Muscle stiffness........ 2. Weight gain........... 3. Dizziness, faintness.. 4. Loneliness............ 5. Headache....... ......... 6. Skin blemish or disorder......... ....... 7. Cold sweats............. 8. Anxiety................. 9. Mood swings.... ...... ... 10. Cramps........... 11. Painful or tender breastOOOIOOOOOOOOIOOOOO 12. Nausea, vomiting........ 13 O CrYing. O O O O O O O O O ..... O O O 14 O BaCRaChe O O O O O O C O O O O O O O O O 15. Swelling (breast, abdomen...... .......... . 16. Hot flashes..... 17. Irritability............ 18. Tension........... 19. FatigueOOOOOOOOOOIOOOOO. 20. Feeling sad or blue..... 21. General aches and painSOOOOOOOOOOOOCOOOOOO 59 Menstrual Distress Questionnaire Form C Write the approximate dates of your most recent menstrual period (flow) in the space marked "A" below. Then write the dates of the menstrual period which preceded the most recent one in the space marked "D". previous menstrual flow from other times four days most recent flow during most before most from to recent cycle recent flow to D C B A On the next two pages is a list of symptoms that women sometimes experience. Please describe your experience of each of these symptoms during the three time periods listed below: Column 1 during your m9§t_;gggnt menstrual flow (the dates shown in area A on the diagram above). Column 2 during the four days before your mes; recent menstrual flow (area B on the diagram). Column 3 during the remainder of your most recent menstrual cycle (area C). Note: The answers you put in columns 1, 2, and 3 should be accurate for your experience during your most recent menstrual cycle. Please do not report your general experience. Also, please report any experience of these symptoms whether or not they seem to be related to your menstrual cycle. For each answer choose the category that best describes your experience of that symptom during that time. Write the number of that category in the space provided. Even if none of the categories is exactly correct, choose the one that best describes your experience. Do not leave any blank spaces. Rudolf H. Moos, Stanford University Medical Center, 1984 e the ecent flo-i' tes rual REFERENCES 64 References Allan, J. D. (1985). Exercise program. In G. Bulechek & J. McCloskey (Ed. ), (pp. 198—219). Nuzsing t ns: atm ts nu s'n dia noses. Philadelphia: W. B. Saunders Company. American College of Sports Medicine (1990). The recommended Quantity of exercise for developing and maintaining cardiorespiratory and muscular fitness in healthy adults. P s' 'o ta American Psychiatric Association (1987). D' s 'c Sggnistigal Mgnual gf Mental Qigongezs (3rd ed. revisedQ, (pp. 367-369). Washington D.C.: American Psychiatric Preff. Barrett, E.A.M. (1988). Using Rogers' science of unitary human beings in nursing practice. Nursing Sciengg Quantenly, ;, 50-51. Boyden, T. W., Pamenter, R. W., Stanforth, P., Rotkis, T. & Wilmore, J. H. (1983). Sex Steroids and endurance running in women. fertilitx_end_§£erilitx, 32(5). 629- 632. Bullen, B. A., Skrinar, G. S., Beitins, I. 2., von Mering, G., Turnbull, B. A., & McArthur, J. W. (1985). Induction of menstrual disorders by strenuous exercise in untrained women. Ihe_Ne1_Englend_lsurnel_2f_uedisine, g12(21), 1349—1353. Burkhart-Lindow, K. (1991). Premenstrual syndrome: Family impact and nursing implications. Jou of Obste r' Gxne22l2gisi_and_Ne2natal_Nur§ins. 22(2). 135-138- Canty, A. P. (1984). Can aerobic exercise relieve the symptoms of premenstrual syndrome (PMS)? Jounnal of §gngol Health, §5(10), 410-411. Carr, 0. 8., Bullen, B. A., Skrinar, G. 3., Arnold, M. A., Rosenblat, M., Beitins, I. 2., Martin, J. 8., & MCArthur, J. W. (1981). Physical conditioning facilitates the exercise-induced decretion of beta-endorphin and beta- lipotropin in women. Ine_Nes_Englsnd_Jgnrnel_2f 52912133, éflifloli 550'552- Caspersen, C., Powell, K., & Christenson, G. (1985). Physical activity, exercise, and physical fitness: Definitions and distinctions for health-related research. Rublis_nealfh_3engrf§.129(2). 126- 131- 65 Cowling, W. R. III (1985). Relationship of mystical experience, differentiation, and creativity. Pe e al Emmekille. 151.. 451-456. Dale, E., Gerlach, D., & Wilhite, A. (1979). Menstrual dysfunction in distance runners. ongtetrics & Q!D§§QlQQ¥: éiflla 47-53- Dalton, K. (1984). T e e strua S d me and (2nd ed.). Chicago: Year Book Medical Publishers Inc. Facchinetti, F., Martignoni, E., Petraglia, P., Sances, M., Nappi, G., & Genazzani, A. R. (1987). Premenstrual fall of plasma B-endorphin in patients with premenstrual syndrome. zerriliry ang Sterility, 11(4), 570-573. - Fair, J., Rosenaur, J., & Thurston, E. (1979). Exercise Management. Wilmer May-June. 13-13. Fawcett, J. (1989). Rogers' science of unitary human beings. In J. Fawcett, ' v t o W cgnge pinnl models or nursing (2nd ed.) (pp 263- 305). Philadelphia: F. A. Davis. Fox, S. M., Naughton, J. P., & Gorman, P. A. (1972b). Physical activity and cardiovascular health. III. The Frequency and type of activity. exercise prescription: Mogern angents gr Cardigygsgulgr Disease, Al, 25-30. Hsia, L. S. Y., & Long, M. H. (1990). Premenstrual syndrome: Current concepts in diagnosis and management. WWW. 15(6) . 351-356. Israel, R. G., Sutton, M., & O'Brien, K. F. (1985). Effects of aerobic training on primary dysmenorrhea symptomatology in college females. Anerigan Journal 9f £211£Q§_fi§elinp £2: 241"244- Johnson, S. R., McChesney, C., & Bean, J. A. (1988). Epidemiology of premenstrual symptoms in a nonclinical Prevalence, natural history and help-seeking sample I. behavior. Journal 9: Reproductive Medicine, ;;(4), 340- 346. Kirkpatrick, M. K., Brewer, J. A., & Stocks, B. (1990). Efficacy of self-care measures for perimenstrual syndrome (PMsl- W. 13. 281-285- Lee, K. A., & Rittenhouse, C. A. (1991). Prevalence of perimenstrual symptoms in employed women. wgngn & Heelin. 11(3): 17'32- 66 Logue, C. M., a Moos, R. H. (1986). Perimenstrual symptoms: Prevalence and risk factors. Esygnosgnatig Mggiging, 48(6). 388-413. LutjeDS. L. R. (1990). Neiee_en_Nureins_Iheeriee (Vol. 1). Martha Rogers: The science of unitary human beings. Newbury Park: Sage Publications. Magos, A. L. & Studd, J. W. (1986). PMS facts and fiction. -Qeniemnererx_gnlfixn. a. 23-24. Merriman, J. E. (1978). Exercise prescription for apparently healthy individuals and for cardiac patients. In K- Wenger (Ed-l. Ezereiee_end_ihe_heeri (pp- 81-92). Philadelphia: F. A. Davis. McArdle, w. 0., Katch, F. 1., & Katch, v. L. (1991). ' ' . e Nutr t' a d u Perfgrnnngg (3rd. ed.). Philadelphia: Lea & Febiger. Moos, R. H. (1985). e ' t ua s to s- A ma ua d ' w' t s a d' . Palo Alto: Stanford University School of Medicine and Veterans Adminstration Medical Centers. M008. R- H- (1991). Eeneirne1.21eireee_92eeiienne1re Mgnngl. Los Angeles: Western Pyschological Services. Piccolo, O. (1982). Effects of biofeedback and autogenic training on symptoms of menstrual distress. (Doctoral disseration, United States International University, San Diego, CA, 1981). sse ' s t te t , .12, 25458. Pollack, M. L. (1971). Effects of walking on body composition and cardiovascular function in middle aged men. Jenrnel_ef_Anelied_£hxeielesx .2. 126- -130- Polit, D. F. & Hungler, B. P. (1991). Nnrsing_3g§ggrgni Brineinlee__nd_neihede (4th ed. ). Philadelphia: J- B. Lippincott Company. Prior, J. C., Vigna, Y., Sciarretta, 0., Alojado, N., & Schulzer, M. (1987). Conditioning exercise decreases premenstrual symptoms: A prospective, controlled 6-month trial. Eeriiliix_end_§ieriliix. 11(3). 402-408- Rapkin, A. J., Chang, L. C., & Reading, A. E. (1988). Comparison of retrospective and prospective assessment of premenstrual symptoms. B§¥Qfl212§i£§l.3§22£§§, .2, 55 60. 67 Rogers, M. E. (1986). Science of unitary human beings. In v. Malinski (Ed-). Exnlereiien_en_Eerine_Beserel_eeienee ' (pp. 4-23). Norwalk, CT: Appletion-Century-Crofts. Rubinow, D. R., & Roy-Bryne, P. (1984). Premenstrual syndrome: Overview from a methodologic perspective. Amer1een_Jesrnel_ef_£exenieirx. 111. 163-172. Shelley, S., & Anderson, C. (1986). The influence of selected variables on the experience of menstrual distress in alcoholic and nonalcoholic women. Jou 0 November/December, 484-491. Smith, M. J. (1984). Human environment process: A test of Rogers' principle of integrality. Adyange§_in_Nnr§ing Seienee. 2(1). 21-28. StanleY. C- T- (1985). Exere1ee_lnieneiix_end_ine_exmniem eexer1ix_ef_nremeneirnel_e¥ndreme. Unpublished master's thesis, California State University, Long Beach, CA. Sveinsdotdtir, H., & Reame, N. (1991). Symptom patterns in women with premenstrual syndrome complaints: A prospective assessment using a marker for ovulation and screening criteria for adequate ovarian function. 1enrnel_ef_Adxeneed_Nureing. 1e. 689-700. Timonen, S., & Procope', B. (1971). Premenstrual syndrome and physical exercise. Aeie_Qbeieirlee_end_§xneeelesx m: at 331-337. Wilhelm-Hass, E. (1984). Premenstrual syndrome: Its nature, evaluation, and management. Jgnrnnl_gfi Qbeieir1e1_exneeelesiel_end_Neeneiel_Nereing..12t4). 223 Woods, N. F., Most, A., & Dery, G. K. (1982). Prevalence of perimenstrual symptoms. e 'c J Heelih. 12(11): 1257-1264- HIGRN STQTE UNIV LIBR IIIIIO II II III II III III 5IIIIIIBII I