Clinical trial Recruiting at 1 site Interventional Ages 17 to 24 Women only

Aerobic Exercise vs. Jacobson’s Relaxation for Primary Dysmenorrhea

Official title: Comparative Effects of Aerobic Exercises and Jacobson's Progressive Relaxation Technique on Pain, Fatigue and Quality of Life in Primary Dysmenorrhea

Run by Riphah International University · NCT07628452 · Data updated 2026-11-12

This study tests whether aerobic exercise or Jacobson’s progressive relaxation can help reduce pain and fatigue and improve quality of life for young women with primary dysmenorrhea.

Quick facts

Study typeInterventional
Ages17 Years to 24 Years
SexWomen only
Enrollment58 (estimated)
SponsorRiphah International University
Academic / other
Locations1 site (Okāra, Punjab Province)
StatusRecruiting
StartedOctober 1, 2025
Main results expectedJuly 1, 2026
Study endsJuly 1, 2026
Registry record updatedJune 5, 2026
Trial IDNCT07628452 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are unmarried, non-athlete women aged 17–24 with mild primary dysmenorrhea and WaLiDD-diagnosed, regular cycles, BMI under 30, and no recent painkiller use.

Probably not a fit

Women with moderate to severe dysmenorrhea, secondary dysmenorrhea, or conditions excluded by WaLiDD criteria may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized trial compares two non-drug approaches for primary dysmenorrhea: aerobic exercise and Jacobson’s progressive relaxation. Participants are 17–24 years old women with mild dysmenorrhea, recruited from selected colleges in Okāra and Lahore, Pakistan, and randomly assigned to one of two groups after screening. Each group receives a different 8-week intervention while both receive baseline core muscle strengthening, with outcomes measured using NPRS for pain, EQ-5D-5L for quality of life, and a fatigue scale. Data collection uses non-probability convenience sampling and sealed envelopes for allocation, with 64 participants divided equally. The study aims to determine which intervention better reduces pain and fatigue and improves life quality.

Why it matters

Potential benefit: If successful, this trial could offer non-pharmacological options to relieve menstrual pain and improve daily functioning for young women.

How similar studies have gone: Previous research suggests non-drug approaches like exercise or relaxation can help dysmenorrhea, but direct head-to-head comparisons are limited and this study adds comparative data.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Pain on numeric rating pain scale,
* Menarche range 12-16,
* BMI less than 30,
* Having a regular menstrual cycle (28-32) days,
* Normal bleeding days (3 to 1) and diagnosed with mild PD according to WaLiDD score

Exclusion Criteria:

* Athletes,
* married women with gynaecological abnormalities were excluded,
* Medical treatment during the study (e.g., oral contraceptives, antidepressants)
* Recent musculoskeletal trauma or surgery, or chronic musculoskeletal disorders
* affecting pain perception (e.g., fibromyalgia, pelvic floor dysfunction)
* secondary dysmenorrhea-related conditions (e.g., endometriosis, fibroids, ovarian cysts),
* consumption of painkillers
* No mental or physical diseases, which reduce the abilities to exercise

Where it's running

  • Superior college for women and Polytechnic institute
    Okāra, Punjab Province, Pakistan
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.