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NCT06157411Completed

Adapting Mindful Eating Program for French Overweight/Obese Population

Validation of a Mindful Eating Program Adapted to the French Population Living With Overweight or Obesity

Source: ClinicalTrials.gov · Last updated 22 Dec 2025

Brief summary (registry, in English)

The aim of this project is to validate a new mindful eating programme adapted to the overweight or obese French population. Recognising the importance of diet in the management of chronic diseases, particularly obesity, and the limitations of traditional weight management approaches, the study focuses on the application of mindful eating. The investigators have adapted a model based on an existing eating disorders programme overseas, taking into account feedback from participants in a qualitative study and the scientific literature. The ultimate aim is to test and validate the effectiveness of this new programme in improving the care of overweight or obese French adults, thereby filling a gap in interventions for this population in France.

Status (registry)
Completed
Study type
Interventional
Enrollment
56 (actual)
First submitted
17 Nov 2023
Start date
16 Feb 2024
Primary completion date
10 Jan 2025
Lead sponsor
University Hospital, Montpellier
Diseases
Obesity
NCT number
NCT06157411

What you commit to

  • Study type: Interventional
  • Participants enrolled: 56
  • From 16 Feb 2024 to the primary completion date, 10 Jan 2025
  • 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

  • People who are taking medicines that may have an effect on their weight (especially GLP-1 analogs, neuroleptics, corticosteroids)

Other illness

  • People who are illiterate or suffer from a major cognitive impairment that prevents them from understanding the study and the mindful eating program
  • Anyone with a history of bariatric surgery or scheduled bariatric surgery within the next 6 months
  • Presence of co-morbidities or severe pathologies (in particular respiratory failure, heart failure, cancer)
  • Diagnosis of severe psychiatric disorder (in particular schizophrenia, bipolar disorder), depressive syndrome, or suicidal behavior in the past year

Other

  • Pregnant or breast-feeding women
  • People suffering from genetic or syndromic obesity
  • Lack of Internet access
  • Person currently participating in another interventional study

Who the study is looking for

  • First visit to the Nutrition and Diabetes Unit of Montpellier University Hospital for overweight/obesity
  • Adults aged 18 and over, volunteers
  • BMI ≥ 25kg/m² and ≤ 50kg/m²
  • Provisional verbal consent followed by signed written consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Antoine Avignon
Coordinator of this site? Confirm its status
MontpellierFranceUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.