No-Pill bloating fix? Video-Guided breathing shows promise
NCT ID NCT06150638
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a non-instrumental biofeedback technique to help people with irritable bowel syndrome or dyspepsia who experience visible abdominal bloating after meals. 41 participants were taught to control their abdominal and chest muscles using a video guide, then practiced the exercises before and after meals for four weeks. The goal was to see if this simple, drug-free approach could reduce the sensation of bloating and changes in belly size.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- biofeedback (behavioral technique)
- What this could lead to
- If it works, this could offer a simple, drug-free way to reduce uncomfortable bloating after meals.
- What could go wrong
- This is a small, early-stage trial with only 41 participants. The technique may not work for everyone, and results need to be confirmed in larger studies.
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
-
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
-
41 people
The number who actually took part.
- Started
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Apr 2024
- Finished
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Jul 2025
- 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
-
18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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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: * episodes of visible abdominal distension triggered by meal ingestion * patients are able to identify the offending foodstuff Exclusion Criteria: * organic cause detected by clinical work-up * constipation * abdominal distension not confirmed by the 7-day clinical questionnaires or after the probe meal in the pre-intervention evaluation
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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
-
Hospital Universitari Vall d'Hebron
Barcelona, 08035, Spain
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Other studies related to the condition(s) this trial covers.
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