NCT05954377Not yet recruiting
Study Assessing the Contribution of Telemedicine Monitoring in Addition to Standard Follow-up of an Obesity Program
Prospective, Single-center, Randomized, Open Label Study Assessing the Contribution of Telemedicine Monitoring in Addition to Standard Follow-up, Strengthening an Obesity Program in Berry (FRANCE)
Source: ClinicalTrials.gov · Last updated 24 Apr 2024 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
STROBERRY Study is a Prospective, monocentric, randomized, open-label study assessing the contribution of telemedicine, in addition to standard follow-up, strengthening an Obesity program in Berry (France). The principal objective is to study the effectiveness of a follow-up reinforced with telemedicine in addition to the standard multidisciplinary annual follow-up on the rate of patients lost to follow-up after initial or second line management in a multidisciplinary bariatric medical program
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 116 (estimated)
- First submitted
- 12 Jul 2023
- Start date
- Sept 2024
- Primary completion date
- Mar 2030
- Lead sponsor
- Elsan
- Diseases
- Obesity
- NCT number
- NCT05954377
What you commit to
- Study type: Interventional
- Planned participants: 116
- From Sept 2024 to the primary completion date, Mar 2030
- 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.
Who the study is looking for
- Woman or Male aged from 18 to 60 years old included
- Patient in obesity (BMI\> or = 30)
- Patient who has completed a multidisciplinary medical program for obesity management, as a first- or second-line intention (after initial obesity management) at the investigating center
- Affiliation to a social security scheme
- Patient informed of the study and who had signed the informed consent form
- Non Inclusion Criteria:
- Management of obesity within the framework of an exclusively interventional program, without redirection to a medical program
- Managing obesity as part of a post-operative program
- Pregnant or breastfeeding women
- Patients deprived of liberty
- Patients under legal protection
Age in the registry: 18 years to 60 years · 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 |
|---|---|---|---|
| Clinique Saint-françois Coordinator of this site? Confirm its status | Châteauroux | France | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.