Remote adapted physical activity program to improve life for adults with IBD

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This pilot interventional program delivers an adapted physical activity (APA) regimen remotely using the MOOV+ application to adults with inflammatory bowel disease. Participants must be at least 18, have a confirmed IBD diagnosis for six months or more, medical clearance for exercise, and internet access; highly physically active individuals are excluded. The program is designed to provide light-to-moderate tailored exercise sessions with remote monitoring and guidance and will measure changes in quality of life and feasibility outcomes. The trial is conducted at GHI Le Raincy Montfermeil and CHU Nantes, with collaboration from Janssen Cilag S.A.S.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Adults aged 18 years and older
* Diagnosis of Inflammatory Bowel Disease (IBD) established for at least 6 months
* Patient is motivated to participate in the Adapted Physical Activity (APA) program
* Medical certificate confirming fitness to engage in remote physical activity
* Access to a digital device with internet connectivity enabling use of the MOOV+ application at home
* Written informed consent freely given after appropriate information
* Affiliation with, or beneficiary of, a national health insurance system

Exclusion Criteria:

* Patients under 18 years of age
* Medical contraindication to physical activity
* High levels of physical activity as defined by the International Physical Activity Questionnaire (IPAQ):

  * Total \>1500 MET-min/week of vigorous activity on at least 3 days, OR
  * Total physical activity \>3000 MET-min/week, regardless of distribution
* Presence of psychological disorders that may interfere with study participation
* Lack of access to a device or internet connection enabling remote participation
* Pregnant or breastfeeding women
* Patients under legal guardianship or curatorship
* Patients under legal protection

Where it's running

• GHI Le Raincy Montfermeil
  Montfermeil, France Recruiting
• CHU Nantes
  Nantes, France Not yet recruiting

Study contacts

• Study coordinator: Stephane NAHON, Professor
• Email: stephane.nahon@ght-gpne.fr
• Phone: +33141708000

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.