Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
250 participants
OBSERVATIONAL
2022-10-10
2023-02-28
Brief Summary
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Detailed Description
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A total of 296 women age of 18-35 participate in the research. Participants were divide into two groups with and without premenstrual syndrome.
Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Group 1 and Group 2
Women With and Without Premenstrual Syndrome
Premenstrual Syndrome Scale, Women's Physical Activity Self-Worth Inventory, Descriptive data
Premenstrual Syndrome Scale, Women's Physical Activity Self-Worth Inventory, Descriptive data
Interventions
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Premenstrual Syndrome Scale, Women's Physical Activity Self-Worth Inventory, Descriptive data
Premenstrual Syndrome Scale, Women's Physical Activity Self-Worth Inventory, Descriptive data
Eligibility Criteria
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Inclusion Criteria
* Being 18-35 years old
* Being women
* To be menstruating
Exclusion Criteria
* Not menstruating for 12 months or more
* Having any psychological diagnosis
* Being pregnant
18 Years
35 Years
FEMALE
No
Sponsors
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Ankara Yildirim Beyazıt University
OTHER
Nigde Omer Halisdemir University
OTHER
Responsible Party
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Asli Celik
MSc. Lecturer
Principal Investigators
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Gürkan Demirtaş, MSc.
Role: PRINCIPAL_INVESTIGATOR
Niğde Ömer Halisdemir University
Arife Akbulut, MSc.
Role: PRINCIPAL_INVESTIGATOR
Ankara Yildirim Beyazıt University
Havva Sümeyye Eroğlu, MSc.
Role: PRINCIPAL_INVESTIGATOR
Gazi University
Locations
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Niğde Ömer Halisdemir University
Niğde, , Turkey (Türkiye)
Countries
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Other Identifiers
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06.10.2022-14
Identifier Type: -
Identifier Source: org_study_id
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