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
NA
80 participants
INTERVENTIONAL
2020-04-06
2020-08-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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interpersonal relations counseling applied
8 sessions of interpersonal relations counseling, each lasting 40 minutes, were applied for 2.
interpersonal counseling
In the intervention group, it will be administered for 40 minutes for 8 weeks to people with symptoms of premenstrual syndrome.
no application
No action taken.
No interventions assigned to this group
Interventions
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interpersonal counseling
In the intervention group, it will be administered for 40 minutes for 8 weeks to people with symptoms of premenstrual syndrome.
Eligibility Criteria
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Inclusion Criteria
2. between the ages of 18-30
3. Menstruating at regular intervals for at least 2 years (21-35 days)
4. Those who have never given birth
5. Speak and understand Turkish
6. It will consist of people who have not received antidepressant, oral contraceptive or hormone therapy for any reason.
Exclusion Criteria
2. A known, ongoing physical health problem (diabetes, rheumatic disease, ...)
3. Any psychiatric disease diagnosed (psychotic disorder, mood disorder, anxiety disorder ...)
4. People who use cigarettes, alcohol or substances
18 Years
30 Years
FEMALE
Yes
Sponsors
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Istanbul University - Cerrahpasa
OTHER
Responsible Party
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Zeynep Seyyide Bozkurt
Principle Investigator
Principal Investigators
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Neslihan Özcan, Professor
Role: STUDY_DIRECTOR
Istanbul University - Cerrahpasa
Locations
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Istanbul University-Cerrahpasa
Istanbul, , Turkey (Türkiye)
Countries
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Other Identifiers
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zeynep
Identifier Type: -
Identifier Source: org_study_id
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