Breathing + core workouts: a new weapon against cramps?
NCT ID NCT07753408
First seen Aug 07, 2026 · Last updated Aug 07, 2026
Summary
This trial tests whether combining breathing exercises with core stabilization exercises relieves menstrual pain better than core exercises alone. It enrolls 48 women aged 18–25 with primary dysmenorrhea, who will attend supervised sessions three times a week for eight weeks. Researchers will measure pain intensity, psychological distress, and quality of life before and after the program to see if the combined approach offers extra benefits.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Breathing exercises combined with core stabilization exercises
- What this could lead to
- If effective, this drug-free exercise combo could offer a simple, accessible way to reduce period pain and improve well-being in young women.
- What could go wrong
- This is a small, early-stage trial, so results may not apply broadly. Benefits over core exercises alone are uncertain, and exercise may not ease severe pain 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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48 people
The number who actually took part.
- Started
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Oct 2025
- Finished
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Apr 2026
- 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 25 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Female participants aged 18-25 years. * Clinical diagnosis of primary dysmenorrhea confirmed through medical history or self-report. * Baseline menstrual pain intensity of 4 or higher on the Visual Analog Scale (VAS). * Willing to participate and provide written informed consent. * Agree not to receive any additional treatment for dysmenorrhea during the study period. Exclusion Criteria * Secondary dysmenorrhea caused by conditions such as endometriosis, adenomyosis, or uterine fibroids. * Pregnancy or childbirth within the previous six months. * Diagnosed pelvic floor disorders or chronic pelvic pain syndrome. * Severe psychological disorders or chronic pain conditions that may interfere with outcome assessment. * Premenstrual Dysphoric Disorder (PMDD). * History of pelvic surgery within the previous 12 months.
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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.
Contacts and locations
Locations
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The University of Lahore
Lahore, Punjab Province, Pakistan
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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