Using a connected scale to improve physical activity programs for chronic disease patients
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
NA · Assistance Publique - Hôpitaux de Paris · NCT06119594
This study is testing if using a connected scale to track body composition can help people with chronic diseases feel better physically and mentally during a six-week rehab program.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 90 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Assistance Publique - Hôpitaux de Paris (other) |
| Locations | 1 site (Paris) |
| Trial ID | NCT06119594 on ClinicalTrials.gov |
What this trial studies
This interventional study aims to assess the impact of a connected impedance scale on the physical and mental quality of life of patients with chronic diseases participating in a rehabilitation program. Participants will be randomized into two groups: one receiving routine care and the other receiving routine care along with the connected scale for monitoring body composition. The study will evaluate whether real-time tracking of body composition can enhance patients' perception of their quality of life over a six-week rehabilitation period. Follow-up assessments will occur at six months to gauge long-term effects.
Who should consider this trial
Good fit: Ideal candidates include adults aged 18 and over with stable, diagnosed chronic diseases who can participate in a physical activity rehabilitation program.
Not a fit: Patients with significant functional limitations or acute medical conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could lead to improved physical and mental well-being for patients with chronic diseases.
How similar studies have performed: While the use of connected devices in rehabilitation is gaining traction, this specific approach combining body composition monitoring with physical activity rehabilitation is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Paris
- Centre d'Investigations en Médecine du Sport - Hôpital Hôtel Dieu — Paris, France (RECRUITING)
Study contacts
- Study coordinator: Pierre FERRAND, Mr
- Email: pierre.ferrand@aphp.fr
- Phone: 0142348985
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Chronic Disease, physical activity rehabilitation program, Connected scale