NCT06133413Active, not recruiting
Connected Scales to Optimize the Maintenance of Weight Lost After Bariatric Surgery and Limit Failures and Reoperations
Source: ClinicalTrials.gov · Last updated 5 Jun 2026
Brief summary (registry, in English)
In this research, we hypothesize that post-operative monitoring implemented with a connected scale after the 1st year (weight nadir period) post obesity surgery (i.e. sleeve and RYGB) would reduce the percentage of patients with excessive weight regain (\>10% regain of lost weight) by improving the quality of follow-up and long-term results. To do this, we are carrying out a comparative study on 182 patients, controlled, randomized per patient, ratio 1/1, open, in two parallel arms. Patients will be followed for 12 months and divided into one of the following two groups: * Control group: Standard follow-up * Interventional group: Standard follow-up + weekly weighing with the "Body Comp Pro" connected scale During their follow-up period, patients in the intervention group will have to weigh themselves at least once a week using the "Body Comp Pro" connected scale. The information will be transmitted to the investigation team via a secure platform available 24 hours a day. Alerts will be generated from a weight regain \> 5% of the baseline weight, allowing early management of weight regain.
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 182 (estimated)
- First submitted
- 30 Oct 2023
- Start date
- 26 Jun 2025
- Primary completion date
- Feb 2027
- Lead sponsor
- Assistance Publique - Hôpitaux de Paris
- Diseases
- Obesity
- NCT number
- NCT06133413
What you commit to
- Study type: Interventional
- Planned participants: 182
- From 26 Jun 2025 to the primary completion date, Feb 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patient with medical-surgical complications during inclusion visit justifying specific and reinforced monitoring (at the discretion of the investigator)
Other
- Patient with a pacemaker
- Patient with a pathology or disability preventing them from standing on the scale
- Patient participating in another interventional research at the time of inclusion
- At the interview, pregnant patient or planning pregnancy during her period of participation in the research
- Patient deprived of liberty
- Patient subject to a legal protection measure (guardianship, curatorship)
Who the study is looking for
- Adult patient aged 18 and over
- Patient operated by a sleeve or RYGB at 1 year (+/- 1 month) from the inclusion visit
- Patient affiliated to a social security system (excluding AME)
- Patient having signed free, informed and written consent
- Patient speaking and reading French fluently
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Hôpital La Pitié Salpetrière Coordinator of this site? Confirm its status | Paris | France | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.