Relaxation technique may soothe IBS symptoms in women
NCT ID NCT07533500
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether a relaxation method called autogenic training can reduce symptoms of irritable bowel syndrome (IBS) in adult women. About 44 women with constipation-predominant IBS will practice relaxation exercises and report changes in pain, bowel movements, fatigue, anxiety, and quality of life. The goal is to see if this mind-body approach offers a drug-free way to manage IBS.
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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 44 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Apr 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 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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20 to 35 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: * Patients diagnosed with irritable bowel syndrome (IBS) based on Rome IV diagnostic criteria constipation- predominant IBS. Their body mass index 25- 30. Exclusion Criteria: * Organic gastrointestinal disorder, thyroid dysfunction, respiratory, renal, hepatic disorder. * Pregnancy, hematological disease, neurological and psychiatric disease. * Previous history of stomach or intestinal excision.
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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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Nisreen Ashraf Helmy
Cairo, Egypt
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Other studies related to the condition(s) this trial covers.
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