Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04639778

Monitoring the Weight Evolution Using a Connected Scale

Led by University Hospital, Lille · Updated on 2025-12-24

390

Participants Needed

2

Research Sites

296 weeks

Total Duration

On this page

Sponsors

U

University Hospital, Lille

Lead Sponsor

M

Ministry of Health, France

Collaborating Sponsor

AI-Summary

What this Trial Is About

Current guideline recommend yearly multidisciplinary postoperative follow-up after bariatric surgery. However, practices remain very heterogeneous, and only a fraction of patients are still follow-up beyond two years after the operation. This study will assess a new care pathway in which the patients are follow-up according to the weight evolution measured by the patient using a connected scale.

CONDITIONS

Official Title

Monitoring the Weight Evolution Using a Connected Scale

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 years or older
  • Patients who had Roux-en-Y Gastric Bypass or Sleeve Gastrectomy bariatric surgery 2 years ago
  • Preoperative Body Mass Index between 35 kg/m2 and 59 kg/m2
  • Access to wired network at home
  • Socially insured patients
  • Patients who signed the informed consent
Not Eligible

You will not qualify if you...

  • Lack of autonomy to use remote monitoring equipment or psychological or psychiatric disorders that prevent optimal use
  • Inability to receive informed consent or participate in entire study due to administrative reasons
  • Lack of social security coverage
  • Refusal to sign consent
  • Patients under guardianship or legal protection

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Ch Boulogne-Sur-Mer - Boulogne Sur Mer

Boulogne-sur-Mer, France, 62321

Actively Recruiting

2

Hop Claude Huriez Chu Lille

Lille, France, 59037

Actively Recruiting

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Research Team

F

François Pattou, MD,PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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