Can massage or music ease period pain? new trial investigates
NCT ID NCT07647276
First seen Jun 26, 2026 · Last updated Jul 01, 2026 · Updated 3 times
Summary
This study tests whether connective tissue massage or music-based relaxation can reduce pain and other symptoms in women with primary dysmenorrhea (painful periods). Thirty-six women will be randomly assigned to massage, relaxation, or a control group. The treatments are given before and during one menstrual cycle, and pain levels are tracked over two cycles.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Connective tissue massage and music-based progressive muscle relaxation
- What this could lead to
- If successful, this could offer drug-free options for managing period pain and related symptoms.
- What could go wrong
- This is a small, early-stage trial with only 36 participants, so results may not apply widely. The interventions are non-invasive but may not work for everyone.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 36 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2026
- Expected to finish
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Nov 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 30 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Pamukkale University, Faculty of Physiotherapy and Rehabilitation
RECRUITINGDenizli, Turkey (Türkiye)
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