- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06636474
Evaluation of the Supported Housing System for the Inclusion of People Suffering From Mental Disorders (EVA-DLAI)
October 9, 2024 updated by: Centre Hospitalier St Anne
Access to housing, in the current context of extreme tension in the rental housing market in Paris and throughout the Ile-de-France region, is proving to be extremely complex for people with mental health problems.National and international scientific studies have quantified the problem of homelessness and precarious or inappropriate housing among patients suffering from psychiatric disorders, and show the impact of housing problems on the consumption of psychiatric care.The DÉLAI's mission is to facilitate access to housing for people enrolled in a psychiatric care pathway, with teams from the psychiatric sectors
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
- Written and oral information provided to the patient by the patient's referring psychiatrist (Investigator of one of the five recruiting sites) during a regular consultation appointment.
- Initial assessment (V inclusion): reminder of the information concerning the research, collection of consent, collection of sociodemographic data, and standardized assessment scales (quality of life, clinical state, level of functioning) + standardized semi-structured interview for the diagnosis of psychiatric disorders + completion by the referring psychiatrist of the data corresponding to the patient's care pathway.
- Then follow-up visit at an annual rate (V1 ... VX), and DLAI exit assessment (V exit) as soon as the patient stops benefiting from the DLAI.
Study Type
Interventional
Enrollment (Estimated)
50
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Alexandra PHAM-scottez, Pr
- Phone Number: + 33 (0)1 45 65 83 70 / 81 08
- Email: a.pham@ghu-paris.fr
Study Locations
-
-
-
Paris, France, 75014
- Recruiting
- Centre Hospitalier Sainte Anne
-
Contact:
- Alexandra PHAM - SCOTTEZ, MD
- Phone Number: +33 145 65 89 18
- Email: a.pham@ch-sainte-anne.fr
-
Principal Investigator:
- Alexandra PHAM - SCOTTEZ, MD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
patient followed for a psychiatric disorder patient benefiting from a DLAI
Exclusion Criteria:
patient not followed for psychiatric disorder patient who refused to participate in the research
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: patients with mental disorders
administration of standardized questionnaires and scales, upon entering the research, then annually, and finally upon leaving the research
|
administration of standardized questionnaires and scales, upon entering the research, then annually, and finally upon leaving the research
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
improvement of quality of life
Time Frame: one year
|
World Health Organization Quality of Life-26,26-item self-assessment questionnaire for assessing quality of life covering four major dimensions: physical health, mental health, social relationships and environment
|
one year
|
|
improvement of quality of life
Time Frame: one year
|
quality of life rating scale (each item is rated from 0 to 6, giving a total score out of 42 points), assessing interpersonal relationships (relationships with close acquaintances and social initiatives), social status, intrapsychic functioning (degree of motivation, anhedonia and capacity for empathy) and regular activities.
|
one year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
clinical condition
Time Frame: one year
|
Mini International Neuropsychiatric Interview : structured diagnostic interview, relatively short in duration, exploring in a standardized way the main psychiatric disorders
|
one year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 27, 2020
Primary Completion (Estimated)
July 27, 2030
Study Completion (Estimated)
December 27, 2030
Study Registration Dates
First Submitted
September 27, 2024
First Submitted That Met QC Criteria
October 9, 2024
First Posted (Actual)
October 10, 2024
Study Record Updates
Last Update Posted (Actual)
October 10, 2024
Last Update Submitted That Met QC Criteria
October 9, 2024
Last Verified
September 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- D20-P007
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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