Telerehabilitation as Follow-up for Obesity

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorCentre de l'Obesite Bernard Descottes

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

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

Trial design

Design model

Parallel

Treatments tested in this trial

  • Aerobic Exercice and muscular reinforcement

    Other intervention

    Aerobic exercise and muscle strengthening to increase weekly physical activity at moderate and vigorous intensities

Treatment groups

138 Participants
are divided into 3 treatment groups
Group A: Supervised TelerehabilitationExperimental treatment 1 intervention
Group B: Unsupervised Physical Activity VideosExperimental treatment 1 intervention
Group C: Contrôle GroupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

MVPA

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).

Time frame
Up to 8 months
2

MVPA

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.

Time frame
Up to 8 months

Secondary outcomes

1

Weight

weight of participants in kilograms

Time frame
Up to 8 months
2

Walking Distance

The walking test will be performed in a corridor delimited by two markers spaced 30 meters apart, following international recommendations (Baillot, Baillargeon, Brown \& Langlois, 2015). The distance is calculated using markers placed on the ground at the end of the test. In addition, dyspnea and perception of effort were measured at the end of the test using the modified BORG scale (0 representing a dyspneic state or non-existent difficulty in exertion and 10 a dyspneic state or perception of maximum effort).

Time frame
Up to 8 months
3

Effort perception and dyspnea

Assessment of perceived exertion and dyspnoea after exercise using the modified Borg scale. This scale ranges from 1 to 10. A score close to 1 shows a perception of effort and a feeling of weak dyspnea. Conversely, the higher the score, the more difficult the effort is perceived.

Time frame
Up to 8 months
4

Lower limb strength

The chair stand-up test will be implemented with a chair placed against a wall. The subject must stand up and sit down as many times as possible from their chair in 30 seconds, without leaning against the backrest and using their hands. This version will be applied since its reliability and reproducibility is greater in subjects whose average age is less than 65 years (Orange et al., 2018).

Time frame
Up to 8 months

Other outcomes

Sponsors and contacts

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