Clinical Trials in France / NCT06871436
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Telerehabilitation as Follow-up for Obesity
NCT06871436 · tracked via the Priya Life Science France tracker
Condition(s) studied
Obese Patients
Investigational drug(s) / intervention(s)
Aerobic Exercice and muscular reinforcement
Aerobic Exercice and muscular reinforcement: Aerobic exercise and muscle strengthening to increase weekly physical activity at moderate and vigorous intensities
Study summary
The goal of this experimental study is to observed the impact of telerehabilitation modalities in obese patient after a hospitalization on physical intensity at home (MVPA). The secondary aim is to observe the evolution of clinical parameters such as anthropometric data, adherence and psychological state.
Eligibility
Inclusion Criteria:
* Adult (\> 18 years old)
* BMI \> 35 or 30 Kg/m2 in case of concomitant comorbidity
* Authorization to practice physical activity for participants over 30 years old by means of a cardiac assessment and an ECG less than 6 months old carried out by a cardiologist. As part of the COBD treatment, the ECG is either: integrated into the patient file before hospitalization if the patient has seen his cardiologist staff. Either the ECG is provided in the file or carried out and analyzed by the center's cardiologist (Dr Rouffaud). The latter then authorizes or not the practice of PA.
* Complete 3-week stay in an obesity center
* Availability of equipment suitable for telerehabilitation at home
* Having given informed consent for participation in the study
Exclusion Criteria:
* Medical contraindication to PA practice defined by a doctor
* Participation in a concomitant research protocol
* For women of childbearing age, they will be informed that in the event of pregnancy occurring during participation in the research, they will not be able to continue the protocol and will withdraw from the research
* Refusal to participate in the research protocol
* Patient on weekday stay (\< 3 weeks)
* Psychiatric/psychological disorder limiting the expression of consent
* Persons under legal protection or unable to express their consent
* Inability to participate in any of the 18 Telerehabilitation sessions
Primary outcome measure(s)
- MVPA — Up to 8 months
Time (min/s) of physical activity at moderate and/or vigorous intensity. This is done with a trivial accelerometer and measures with an equation (Garmin) the MVPA practice time over a week and gives a value in minutes per week. It enables us to understand whether or not a participant is achieving the recommended level of physical activity (150 min/week at moderate or vigorous intensity). - MVPA — Up to 8 months
This questionnaire by Craig et al (2003) consists of 27 questions divided into 5 parts. In each part, the participant is asked to quantify the amount of time in minutes/hours/days spent in PA. The first part comprises questions 1 to 7 and covers all physical activity practised in a professional context. The second part, questions 8 to 13, covers physical activity related to daily commuting (walking, cycling, driving, etc.) (to work, to the stores, etc.). The third part comprises questions 14 to 19 and covers activities related to housework, home maintenance, time spent with family, etc. The fourth part, questions 20 to 25, deals with physical activity related to leisure, sport and free time. Finally, the fifth section includes questions 26 to 27 and covers time spent sitting or lying down during the day.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Bernard Descottes Obesity Center | Saint-Yrieix-la-Perche | France |
Other trials for the same condition
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06871436 on ClinicalTrials.gov ↗ ← All trials in France