Study seeks to predict who thrives after Weight-Loss surgery
NCT ID NCT06951893
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows 165 adults undergoing bariatric surgery to see if certain pre-surgery traits—like anxiety, depression, eating behaviors, and weight-related quality of life—can predict how their quality of life changes over the two years after surgery. Participants complete questionnaires and have their weight and body measurements taken at several points before and after surgery. The goal is to identify patterns that could help tailor support to individual patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could help doctors identify which patients are likely to have the best quality-of-life improvements after bariatric surgery, allowing for more personalized care.
- What could go wrong
- This is an observational study, not a treatment trial, so it won't directly change outcomes. Results may not apply to all patient groups or surgical programs.
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 165 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2025
- Expected to finish
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Sep 2030
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 years and older
- Sex
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Anyone
- 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: * patient \> 18years old * Integrated into the GEROM73 surgical program and starting the intra-hospital program Exclusion Criteria: * Patients in a state of psychiatric decompensation * Patients with cognitive disorders * Patients with difficulties understanding the French language, spoken or written * Pregnant, parturient, or breastfeeding women
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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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Centre Hospitalier Métropole Savoie
RECRUITINGChambéry, Savoie, 73011, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can Weight-Loss surgery patients skip the opioids?
- Can tailoring bypass length improve weight loss surgery results?
- New injection IBI3046 tested for weight management
- Can collagen supplements help preserve muscle after Weight-Loss surgery?
- Blood markers may predict muscle loss after Weight-Loss surgery