Clinical trial

Study Assessing the Contribution of Telemedicine Monitoring in Addition to Standard Follow-up of an Obesity Program

Opening soon · Not applicable · 1 countries · Registry ID NCT05954377

Opening soonNot applicableInterventional

What this study is about

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

A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.

Basic eligibility

Age18 Years to 60 Years

SexAll

Healthy volunteersNot accepted

ConditionObesity

Full registry criteria

Inclusion Criteria: * 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

Treatments and study arms

Quarterly remote motivational interviews

Other

Remote motivational interview will be in the form of quarterly telephone call (at 3, 6 and 9 months after the start of annual follow up; the patient is seen again at 12 months as part of the annual follow-up) and this for 4 years. It will be performed by medical staff trained in motivational interviewing and who have completed at least 40 hours training in therapeutic education

Primary outcomes

Rates of patients lost to follow up4 years

Rates of patients lost to follow up measured in both arms and compared 4 years after randomization

Study locations

1 locations were listed when this page was built. The first 40 are shown.

Clinique Saint-François🇫🇷 Châteauroux, France

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Françoise LEVITTA, MDContact

Email · Call 06 78 57 01 42