RecruitingNot ApplicableNCT06133413

Connected Scales to Optimize the Maintenance of Weight Lost After Bariatric Surgery and Limit Failures and Reoperations


Sponsor

Assistance Publique - Hôpitaux de Paris

Enrollment

182 participants

Start Date

Jun 26, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This randomized controlled study tests whether using a connected (smart) scale for weekly home weigh-ins can reduce excessive weight regain in adults who had bariatric surgery (sleeve gastrectomy or gastric bypass) one year earlier — a period when weight regain commonly begins. Patients in the intervention group weigh themselves weekly using the Body Comp Pro smart scale, which transmits data to the care team; automatic alerts are triggered if weight regain exceeds 5%, allowing early intervention. Adults aged 18 and older who had sleeve gastrectomy or gastric bypass exactly one year prior (plus or minus one month), speak and read French fluently, and do not have a pacemaker or medical complications requiring intensive monitoring are eligible. Participants are followed for 12 months, comparing weight regain between the connected scale group and a standard follow-up control group. This summary was prepared as patient-facing educational content using AI assistance.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEBody Comp Pro connected scale (Withings manufacturer)

Use once a week

OTHERAlert generation by remote plateform

Alert will be generated from weight regain \> 5% of baseline weight


Locations(1)

Hôpital La Pitié Salpêtrière

Paris, France

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NCT06133413


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