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Completed NCT04887077

Digital Intervention Promoting Physical Activity Among Obese People (DIPPAO)

Conditions: Obesity, Diabete Type 2

Sex: All
Ages: 18 Years – 65 Years
Healthy volunteers: No
Phase: NA
Enrollment: 56
Sponsor: University Hospital, Clermont-Ferrand

Location: CHU de Clermont-Ferrand Clermont-Ferrand

Summary

Overweight and obesity are today considered among the most important health risks facing humanity with more than one in two adults overweight or obese in western countries. In addition, Type 2 diabetes mellitus (T2DM) is a common comorbidity associated with overweight and obesity and counts for 5% of the French population under 65 years of age and 15% in people over 65 years old. Despite the accumulation of scientific evidence supporting the benefits of physical activity, obese and diabetic people remain insufficiently active and current programs struggle to engage and sustain physical activity of patients over long periods of time. It is therefore urgent to develop interventions that can effectively change individuals' behavior. In this context, "e-health" interventions and gamification appear to be a particularly promising avenue to improve physical activity and reduce attrition rates of current programs. This clinical trial aim to test the effectiveness of a digital intervention based on gamification and teamwork in comparison to a supervised physical activity program. The investigators hypothesized that the intervention will be efficient by the development of a self-determined motivation through the process of gamification on the one hand. On the other hand, through the in-group collaboration with other people who share the same stigmatized criteria that will help participants to overcome weight stigmas, acting generally as physical activity barriers.

Eligibility Criteria

Inclusion Criteria: * Subject affected for obesity (BMI ≥30 kg/m² and \ 2 to 3 drinks per day depending on gender) or drug addiction. * Disability or contraindication to PA. * Subject with cardiorespiratory and/or osteoarticular disorders that limit their ability to perform physical tests or moderate PA for 30 minutes. * Subject with progressive cardiovascular or neoplastic disease. * Subject who has presented a major infection in the 3 months prior to inclusion. * Subject with a known neuro-muscular pathology (i.e., myopathy, myasthenia, rhabdomyolysis, paraplegia, hemiplegia). * Subject with chronic or acute inflammatory pathology within 3 months prior to inclusion. * Subject diagnosed and/or treated for schizophrenia, bipolar disorder, major depression. * Subject deprived of their liberty by judicial or administrative decision. * Subject refusing to sign the written consent to participate. * Subject participating in another study.

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT04887077). StuddyBuddy aggregates publicly available trial information.