Actively Recruiting
Comparison of Myofascial Release and Kinesiotaping Techniques in the Management of Primary Dysmenorrhea
Led by Medipol University · Updated on 2025-08-01
46
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate the effects of two physiotherapy techniques, myofascial release therapy (MRT) and kinesiotaping (KT), in managing primary dysmenorrhea, which is painful menstruation without any underlying medical condition. Dysmenorrhea affects many women worldwide, causing severe cramps and impacting quality of life. This study focuses on women aged 18 to 30 years who experience moderate to severe pain during their menstrual cycle. Participants will be randomly assigned to one of two groups. One group will receive a single session of myofascial release therapy targeting various abdominal and back fascial layers to relieve tension. The other group will receive kinesiotaping using a specific three-tape sensory modulation method applied to the lower abdomen and sacral area to address pain and fascial tension. Both interventions will be done on the participant's most painful menstrual day. During the study, participants will complete questionnaires before treatment, 8 hours after, and again 3 to 5 weeks later during their next menstrual cycle. These include a pain scale (Visual Analog Scale) and a quality of life assessment (PROMIS-29 Profile v2.0). The research team will analyze these measures to compare the treatments' effects on pain and quality of life. The study is planned to end in October 2025 and involves careful monitoring of participants' responses over time.
CONDITIONS
Brief Title
Comparison of Different Physiotherapy Techniques in Dysmenorrhea
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of primary dysmenorrhea
- Moderate-to-severe pain during menstrual days 1-3
- Regular menstrual cycles for past 6 months
- Female sex
- Age between 18 and 30 years
You will not qualify if you...
- Secondary gynecological conditions
- Current use of pain medications
- History of pregnancy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants receive a single session of either Myofascial Release Therapy or Kinesio Taping on their most painful menstrual day to relieve primary dysmenorrhea symptoms.
1 treatment visit (in-person)
Duration - 3 to 5 weeks
Participants complete questionnaires to assess pain and quality of life before treatment, 8 hours after treatment, and during their first menstrual cycle 3-5 weeks post intervention.
2 follow-up assessments (remote or in-person)
Trial Site Locations
Total: 1 location
1
İstanbul Medipol University
Istanbul, Beykoz, Turkey (Türkiye), 34810
Actively Recruiting
Research Team
S
Salma Abdelzaher
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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