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RECRUITING Not applicable ClinicalTrials.gov

Fitness and Well-being of Caregivers in the Hauts-de-France Region

Sponsor: Lille University • ClinicalTrials.gov ID: NCT06832709

Registry updated: 2026-09-10
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Description

The ageing of the population is accompanied by an increase in the frequency of chronic illnesses, leading to a rise in the number of caregivers. These caregivers do not have the time to look after their own health, and they are very often in a deteriorated mental state with no knowledge of their level of fitness. A deterioration in their fitness can be a source of the development of diseases induced by a sedentary lifestyle. On the other hand, patients with chronic respiratory disease can benefit from respiratory rehabilitation (RR), which includes outpatient or home-based physical activity. The literature has demonstrated an improvement in the mental state of caregivers following a RR carried out by their loved ones without taking an interest in their fitness. The aim of the study will be to establish 1. a representation of the level of fitness and mental state of caregivers; 2. to assess the presence/absence of benefits on fitness and mental state of caregivers depending on the form of RR: home versus outpatient where the caregiver is not integrated in this last form.

Interventions

  • a program of rehabilitation (Other)
    physical activities, health education, psychosocial and motivational support

Eligibility criteria

Inclusion Criteria: * Be of legal age; * Have a sick relative taking part in a RR program, either as an outpatient at the Clinique de la Mitterie or at home with FormAction Santé; * Have the cognitive ability to understand the instructions for carrying out the physical tests and the questions for answering the questionnaires; * Be able to read; * Have no disability preventing them from carrying out the physical tests; * Have given their written consent to take part in the research; * Be willing to comply with all the research procedures and duration. Exclusion Criteria: * Refusal to sign consent; * Operation less than one month old; * Presence of psychological or psychiatric disorders; * Impossibility of receiving informed information; * Impossibility of participating in the entire study; * Contraindication to physical activity.

Conditions

Healthy

Locations

  • Participant'S Home — Lille, France
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Official Source

Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

View Official Record