Contribution of the Evaluation of Body Composition by Connected Scale in the Effectiveness of a Reconditioning Program Through Physical Activity Adapted for Patients Suffering From Chronic Diseases (COCORAPA)

Assistance Publique - Hôpitaux de Paris

Status: Active, not recruiting

Conditions: Chronic Disease

Treatments: Device: Body Comp Pro connected scale (Withings manufacturer)

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT06119594

2023-A01156-39 (Other Identifier)

APHP230549

Details and patient eligibility

About

The goal of this interventional study is to evaluate the impact of the use of a connected impedance scale on the physical and mental quality of life of patients suffering from chronic diseases and participating in a physical activity rehabilitation program. The main objective is to know if a regular monitoring of the evolution of body composition parameters recorded by the connected scale would allow patients participating in the Physical Activity rehabilitation program at Hôtel-Dieu to follow in real time the effects of such program, not on weight itself but on body composition, and that this would contribute to a better perception of physical and mental quality of life at the end of the program 90 Participants will be randomized in two groups :

• Control group (N = 45) : routine care
• Interventionnal group (N=45) : routine care + use of connected scale All participants will undergo physical activity rehabilitation program during 6 weeks.

Patients will be see again at 6 months, and the following parameters will be comparer between the two groups :

• SF-36 questionnaire
• Ricci & Gagnon questionnaire
• 6MWT
• 30 sec sit-to stand test
• Ito-Shirado test
• Sorensen test
• Handgrip test
• MaxV02

Enrollment: 90 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patient (male or female) aged 18 and over
• Patient able to express free, informed and written consent
• Patient participating in the physical activity rehabilitation program at the CIMS of the Hôtel Dieu
• Patient suffering from a known, stable and diagnosed chronic disease
• Patient autonomous in taking treatments for their ALD
• Patient affiliated to a social security system

Exclusion criteria

• Patient under legal protection (guardianship, curatorship)
• Patient deprived of liberty by a judicial or administrative decision
• Patient with functional limitations that do not allow a physical assessment or result in a walking distance < 350 m during the HDJ for admission to the program
• Patient with suspected cardiac pathology during the HDJ for admission to the program
• Patient with episode of decompensation or exacerbation
• Patient with a pacemaker or implantable automatic defibrillator
• Pregnant women

Trial design

Primary purpose: Diagnostic

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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90 participants in 2 patient groups

Standard follow-up group

No Intervention group

Description:

Routine care

Connected scale group

Experimental group

Description:

Routine care + use of connected scale during 6 months

Treatment:

Device: Body Comp Pro connected scale (Withings manufacturer)