Study to reveal how Weight-Loss surgery alters your sense of body and eating
NCT ID NCT07594275
First seen Jun 27, 2026 · Last updated Sep 04, 2026 · Updated 2 times
Summary
This study looks at how people with severe obesity perceive internal body signals (like hunger and fullness) before and after bariatric surgery. Researchers will follow 300 adults for two years to see if changes in body awareness and views on illness affect eating behaviors after surgery. The goal is to better understand psychological factors that influence long-term weight and eating outcomes.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 300 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2026
- Expected to finish
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May 2028
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.
Who is studied
The study population consists of adults with severe or morbid obesity undergoing pre-operative multidisciplinary evaluation for bariatric surgery at a tertiary referral center. Participants are assessed before surgery and during post-surgical follow-up as part of routine clinical care.
- 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: * Adults aged 18 years or older. * Diagnosis of severe or morbid obesity (body mass index ≥35 kg/m² with obesity-related comorbidities or ≥40 kg/m²). * Undergoing multidisciplinary evaluation with indication for bariatric surgery. * Ability to provide informed consent and complete self-administered questionnaires. Exclusion Criteria: * Age younger than 18 years. * Presence of neurological disorders associated with cognitive impairment that may interfere with questionnaire completion. * Pregnancy or breastfeeding at the time of enrollment. * Inability to complete study assessments due to language barriers or other conditions limiting participation.
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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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Fondazione Policlinico Universitario A. Gemelli IRCCS
RECRUITINGRome, Lazio, 00168, Italy
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Other studies related to the condition(s) this trial covers.
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- Can a cold cloth on the neck calm Post-Surgery nausea?