Status:
NOT_YET_RECRUITING
The The Effect of Planned Behavior Theory-Based Education on Physical Activity and Dysmenorrhea
Lead Sponsor:
Ankara University
Conditions:
Dysmenorrhea Primary
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
The aim of the study is to examine the effect of the planned behavior theory-based education program applied to university students with primary dysmenorrhea on physical activity behavior and dysmenor...
Detailed Description
The study was planned to be conducted as a randomized controlled experimental study in the pre-test-post-test order. The research was planned to be conducted at Bitlis Eren University. The population...
Eligibility Criteria
Inclusion
- Last menstrual pain is 5 points or more out of 10 on the Visual Pain Scale (moderate/severe/unbearable pain),
- Being 18 years or older,
- Reading and writing Turkish,
- Receiving education at undergraduate level,
- Being a first year student,
- Being nulliparous (never giving birth) and never having had a pregnancy,
- Having a regular menstrual cycle (every 21-35 days, lasting 3-8 days and without complaints of intermittent bleeding) for the last 6 months,
- Being inactive or minimally active according to the International Physical Activity Survey,
- Being diagnosed with primary dysmenorrhea by the physician,
- Agreeing to participate in the study.
Exclusion
- Receiving education at the health vocational high school level,
- Last menstrual pain is 4 points or less out of 10 on the Visual Pain Scale,
- Having any gynecological diagnosis (endometriosis, ovarian cyst, myoma, polyp, etc.),
- Having undergone a gynecological operation (hysterectomy, myomectomy, etc.),
- Being on hormonal drug therapy,
- Having an orthopedic disability (congenital limb deficiencies, congenital hip dislocation, scoliosis, meningomyolocele, cerebral palsy, etc.), visual disability (vision loss, peripheral retinopathy, hemianopia, night blindness, etc.) and hearing disability that would prevent physical activity,
- Having acute or severe pain that increases with movement,
- Having a known systemic and chronic disease (diabetes, heart disease, vascular diseases, circulatory disorders, varicose veins, blood diseases, etc.),
- Having any psychiatric diagnosis (depression, anxiety disorder, etc.)
- Not agreeing to participate in the study.
Key Trial Info
Start Date :
January 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
January 1 2024
Estimated Enrollment :
68 Patients enrolled
Trial Details
Trial ID
NCT06210659
Start Date
January 1 2024
End Date
January 1 2024
Last Update
January 18 2024
Active Locations (1)
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1
Bitlis Eren University
Bitlis, Turkey (Türkiye)