PRACOH Prevention Breakdown Support Advice Guidance Disability
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorPôle Saint Hélier
About this trial
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.
Eligibility criteria
Qualifiers
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
Disqualifiers
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.
Trial design
Treatments tested in this trial
- 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.
Treatment groups
100 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov