Tests remote check-ins alongside usual follow-up for adults with obesity
Tests remote motivational check-ins added to usual care for adults with obesity.
Plain-language title generated from the registry record
Registry title: Study Assessing the Contribution of Telemedicine Monitoring in Addition to Standard Follow-up of an Obesity Program
Key facts
- Where
- Châteauroux, FranceSee the site
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 18 and 60 years old?
Source: NCT05954377, who can take part
Where in France
- Clinique Saint-françoisChâteauroux, FranceNo longer taking part
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Elsan
- Trial code
- NCT05954377
- Record updated
- 24 April 2024
- Original description
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 programRead full original descriptionShow less
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)
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
Inclusion: 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.