- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05692479
Premenstrual Syndrome and Physical Activity Self-Worth
Comparison of Physical Activity Self Worth of Women With and Without Premenstrual Syndrome
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Premenstrual syndrome (PMS) negatively affects the quality of life of millions of women. PMS is a common cyclic disorder characterized by somatic, cognitive, emotional and behavioral symptoms that usually occurs in young and middle-aged women, lasts during the luteal phase of the menstrual cycle and ends with the onset of menstruation.Studies have shown that women with high PMS symptoms are more inactive. Physical activity participation in women affects a wide spectrum of self-perceptions, including knowledge, social, and emotional self-perceptions. By determining which physical, emotional, social and academic/knowledge areas are affected by women, increasing their participation in physical activity can be achieved. The subject of the study is to determine the symptom severity of women with and without premenstrual syndrome and to examine how premenstrual syndrome affects physical activity self-worth.
A total of 296 women age of 18-35 participate in the research. Participants were divide into two groups with and without premenstrual syndrome.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Niğde, Turkey, 51200
- Nigde Omer Halisdemir University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Volunteer to participate in the study
- Being 18-35 years old
- Being women
- To be menstruating
Exclusion Criteria:
- Evaluation form missing
- Not menstruating for 12 months or more
- Having any psychological diagnosis
- Being pregnant
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Group 1 and Group 2
Women With and Without Premenstrual Syndrome
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Other: Premenstrual Syndrome Scale, Women's Physical Activity Self-Worth Inventory, Descriptive data
Premenstrual Syndrome Scale, Women's Physical Activity Self-Worth Inventory, Descriptive data
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Descriptive Data
Time Frame: Baseline
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In the general evaluation form, data such as age, gender, weight, height, age at menarche, menstruation interval, menstrual pattern, presence of gynecological problems, presence of dysmenorrhea, pain level, exercise status, presence of chronic disease will be recorded.
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Baseline
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Premenstrual Syndrome Scale
Time Frame: Baseline
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The Premenstrual Syndrome Scale (PMSS) was developed by Gençdoğan in 2006, based on DSM III and DSM-IV, and its validity and reliability were established.
PMSS is a 44-item five-point Likert-type scale.
After each item is read in PMSS, marking is made by taking into account the degrees to the right of the relevant item, depending on whether this situation is within the period of "one week before menstruation".
In scoring the scale, "Never" is evaluated as 1, "Very little" as 2, "Sometimes" as 3, "Often" as 4, and "Constantly" as 5 points.
A score of 138 or higher indicates PMS.
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Baseline
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Women's Physical Activity Self-Worth Inventory
Time Frame: Baseline
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The Women's Physical Activity Self-Worth Inventory (Women's Physical Activity Self-Worth Inventory), developed by Huberty J. et al. in 2013, is a 37-item multidimensional scale.
Turkish version study, validity and reliability were done by Yutçiçek and Kömürcü in 2019.
FAESQ is a 37-item Likert-type (Strongly Disagree (1), Disagree (2), Agree, (3), Strongly Agree (4)) scale that evaluates the non-physical aspects of physical activity-related self-worth in women.
The total score obtained from the scale varies between 37 and 148.
As the score increases, the sense of self-worth increases.
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Baseline
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Gürkan Demirtaş, MSc., Nigde Omer Halisdemir University
- Principal Investigator: Arife Akbulut, MSc., Ankara Yildirim Beyazıt University
- Principal Investigator: Havva Sümeyye Eroğlu, MSc., Gazi University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 06.10.2022-14
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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