Actively Recruiting

Phase Not Applicable
Age: 17Years - 25Years
FEMALE
ID06777940

Effects of Kegel Exercises With and Without Myokinetic Active Release of Trigger Points on Pain, Fatigue and Quality of Life in Primary Dysmenorrhea

Led by Riphah International University · Updated on 2025-01-16

50

Participants Needed

2

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating the effects of exercise on primary dysmenorrhea, a common condition causing painful menstrual cramps in young women. This study aims to evaluate whether myokinetic active release of trigger points in specific muscles is more effective than Kegel exercises alone in reducing pain, fatigue, and improving quality of life. The study addresses a gap in current knowledge about combined exercise interventions and their impact on this condition in females aged 17 to 25 years. Participants will perform Kegel exercises combined with myokinetic active release therapy targeting trigger points in the quadratus lumborum, rectus abdominis, and gluteus medius muscles. The therapy involves sustained pressure applied passively for 8-10 seconds, combined with pelvic floor muscle tightening and relaxing exercises. Participants will do 30 repetitions per session following a hold and relax pattern over an 8-week intervention period. During the study, researchers will assess pain levels using a numerical pain rating scale, fatigue severity with the Fatigue Severity Scale (FSS), and quality of life through the SF-36 questionnaire. These assessments are conducted at the start and end of the 8-week treatment. The study is sponsored by Riphah International University and aims to provide evidence about the functional impact of these exercises on young women suffering from primary dysmenorrhea.

CONDITIONS

Brief Title

Effects of Kegel Exercises and Myokinetic Release of Trigger Points in Primary Dysmenorrhea

Who Can Participate

Age: 17Years - 25Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 17-25 years
  • Diagnosed cases of dysmenorrhea
  • Presence of trigger points in rectus abdominis, quadratus lumborum, and gluteus medius muscles
  • Regular menstrual cycles of 21-35 days lasting 3-7 days
Not Eligible

You will not qualify if you...

  • Use of oral contraceptives for menstrual irregularity
  • Other gynecological diseases such as fibroids or endometriosis
  • Use of analgesics
  • Presence of endometrial polyp, pelvic infection, use of IUD, or venous congestion in internal genital organs

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 - 8 weeks

Participants perform Kegel exercises combined with Myokinetic active release of trigger points targeting specific muscles to help reduce pain and fatigue and improve quality of life in primary dysmenorrhea.

Regular sessions during the 8-week treatment period

Trial Site Locations

Total: 2 locations

1

Major balqees maternity home

Lahore, Punjab Province, Pakistan, 53201

Actively Recruiting

2

Major Balqees Maternity Home Clinic

Lahore, Punjab Province, Pakistan

Actively Recruiting

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Research Team

I

imran NA amjad, phd

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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