RECRUITING Not applicable ClinicalTrials.gov

PRACOH Prevention Breakdown Support Advice Guidance Disability

Sponsor: Pôle Saint Hélier • ClinicalTrials.gov ID: NCT07496996

Registry updated: 2026-09-15

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Description

The main objective of this prospective interventional study is to evaluate the impact of the stay in the dedicated transitional care unit, through the achievement of the patient's primary objective set at admission, directly related to their specific needs. It is expected to improve knowledge regarding the prevention of situations of breakdown and exhaustion in the living environment of people with disabilities. * This would improve the life and care pathways as well as the support provided to these individuals and their families and friends. * It would limit the use of unscheduled care services in crisis situations, thereby improving the quality of care and life.

Interventions

the impact of the stay in the dedicated transitional care unit by evaluating whether the patient's primary objective, set at admission and directly related to their specific needs, has been achieved. (Other)
assess the impact of the stay in the dedicated transitional care unit by evaluating whether the patient's primary objective, set at admission and directly related to heir specific needs, has been achieved.

Eligibility criteria

Inclusion Criteria: * Patients: * People with disabilities requiring a 4-week stay in a dedicated transitional care unit at POLE MPR ST HELIER * Men or women, of legal age (over 18) * Affiliated with a social security scheme or entitled to benefits * Having given their free and informed consent * Caregivers: * Primary caregiver from the circle of a person with a disability who has agreed to participate in the study. * Male or female, of legal age (over 18) * Affiliated with a social security scheme or entitled to benefits * Having given their free and informed consent Exclusion Criteria: * Patients: * Pregnant women, women in labor, or women who are breastfeeding * Individuals deprived of their liberty by judicial (excluding guardianship or curatorship) or administrative decision * Individuals undergoing severe psychiatric treatment that may impact the conduct of the protocol, at the investigator's discretion * Individuals in an emergency situation who are unable to give their prior consent. * Caregivers: * Professional caregivers of participants with disabilities who have agreed to participate in the study. * Pregnant women, women in labor, or women who are breastfeeding, * Individuals deprived of their liberty by a judicial (excluding guardianship or curatorship) or administrative decision. * Individuals undergoing severe psychiatric treatment that may impact the conduct of the protocol, at the investigator's discretion * Individuals in an emergency situation who are unable to give their prior consent.

Conditions

Person With a Disability Caregiver

Locations

Fondation Saint-Hélier — Rennes, France

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Official Source

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

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