Connective Tissue Massage and Music-based Relaxation for Period Pain
Official title: The Effects of Connective Tissue Massage and Music-Based Progressive Muscle Relaxation on Pain Intensity, Pressure Pain Threshold, and Menstruation-Related Symptoms in Women With Primary Dysmenorrhea: A Randomized Controlled Trial
Run by Pamukkale University · NCT07647276 · Data updated 2026-11-12
This study tests whether connective tissue massage or a music-based relaxation program can reduce pain and related symptoms in young women with primary dysmenorrhea.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 30 Years |
| Sex | Women only |
| Enrollment | 36 (estimated) |
| Sponsor | Pamukkale University Academic / other |
| Locations | 1 site (Denizli) |
| Status | Recruiting |
| Started | June 22, 2026 |
| Main results expected | October 30, 2026 |
| Study ends | November 15, 2026 |
| Registry record updated | June 30, 2026 |
| Trial ID | NCT07647276 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are women aged 18–30 with clinically diagnosed primary dysmenorrhea, regular cycles, and a history of menstrual pain higher than 4 cm on the Visual Analog Scale.
✕Probably not a fit
Individuals with gastrointestinal, autoimmune, psychiatric, or pelvic conditions, or those on chronic analgesic or psychotropic therapy, 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, three-arm trial assigns women with primary dysmenorrhea to receive connective tissue massage, music-based progressive muscle relaxation, or no intervention as a control. Interventions occur from the estimated ovulation day in Cycle 0 through Cycle 1, with post-intervention and follow-up assessments in Cycle 2. Outcomes include pain intensity, pressure pain threshold, analgesic use, and menstrual symptoms. Baseline and follow-up visits are scheduled during specific days of menstrual cycles to standardize assessment. The study aims to determine if these nonpharmacologic approaches can alleviate menstrual pain and improve related symptoms.
Why it matters
Potential benefit: If successful, participants may experience reduced menstrual pain and fewer related symptoms, potentially lowering analgesic use.
How similar studies have gone: Previous studies suggest nonpharmacologic approaches can help with menstrual pain, but results vary by method and population.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Having a diagnosis of primary dysmenorrhea made by a Gynecology and Obstetrics specialist * Being between 18-30 years of age * Being nulliparous * Having a regular menstrual cycle (28 ± 7 days) * Having menstrual pain intensity greater than 4 cm on the Visual Analog Scale for the last 6 months * Voluntarily agreeing to participate in the study Exclusion Criteria: * Having been diagnosed at least 6 months prior with gastrointestinal, urogynecological, autoimmune, or psychiatric diseases and/or chronic pain syndromes * Having any neurological or systemic disease * Having a history of childbirth or previous pregnancy * Being pregnant * Using an intrauterine device (IUD) * Having any pelvic pathology or history of pelvic surgery * Chronic use of medications, including oral contraceptives or antidepressants * Currently receiving anti-inflammatory, analgesic, or psychotherapeutic drug treatment * Having irregular menstrual cycles (\<21 or \>35 days and/or cycle variation \>4 days) * Presence of pathology indicating secondary dysmenorrhea
Where it's running
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Pamukkale University, Faculty of Physiotherapy and Rehabilitation
Denizli, Turkey (Türkiye) Recruiting
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.