Talking before cutting: therapy boosts Weight-Loss surgery success?
NCT ID NCT03976674
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a short therapy program before weight-loss surgery helps patients develop healthier eating habits. About 94 adults preparing for bariatric surgery took part. The goal was to see if the program could improve long-term results by addressing emotional eating and dietary restrictions.
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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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94 people
The number who actually took part.
- Started
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Feb 2018
- Finished
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Sep 2020
- 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 60 years
- 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 starting a preparation for bariatric surgery in the endocrinology department at St Philibert Hospital * 18 ≤Age≤60 years * Patient meeting the criteria of the High Authority of Health (HAS) for the agreement of a bariatric treatment * Patient affiliated to the social security * Patient giving informed consent Exclusion Criteria: * Low level of comprehension of French * Pregnant women * Patient under guardianship or curatorship.
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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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• Lille Catholic University Hospital Group, Saint Philibert Hospital
Lomme, Haits de France, 59, France
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Other studies related to the condition(s) this trial covers.
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