Actively Recruiting

Phase Not Applicable
Age: 18Years - 30Years
FEMALE
ID07022106

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

Age: 18Years - 30Years
FEMALE

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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)

Follow-up

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

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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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