- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02857296
Evaluative Research in the Process of Implementation of an Alternative Device to Hospitalization for People Homeless With Severe Psychiatric Disorders (REDAP)
August 2, 2016 updated by: Assistance Publique Hopitaux De Marseille
The research project aims to analyze the implementation of a new health care system - "alternative device to hospitalization and crisis home for people without home" - whose objective is to provide the homeless and suffering from severe psychiatric disorders adequate care to prevent situations from seeking care or complication of their disease.
This device, if it has the administrative and legal structure of the Twin Stop Health Care (LHSS), is based on the original concept of "Soteria House."
This will build tools for evaluating the performance of care device by a process evaluation describing and analyzing what activity involves the device, This research seeks to analyze the experimental device in the early stages of its implementation.
The observation and analysis of the program period will adjust the management arrangements of the device.
The data and conclusions from this research will identify the contributions and benefits of such a device and analyze the difficulties encountered in its implementation.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
30
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Adults without home, with severe psychiatric disorders;
Description
Inclusion Criteria:
Adults without home with severe psychiatric disorders utilizing the structure, adults who master the French language
Exclusion Criteria:
adults not mastered the French language
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
socio-anthropological survey
Time Frame: 1 year
|
Biographical interviews and three du'entretiens targeted series on the course therapy will be conducted
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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
January 1, 2017
Primary Completion (Anticipated)
January 1, 2020
Study Completion (Anticipated)
July 1, 2020
Study Registration Dates
First Submitted
July 29, 2016
First Submitted That Met QC Criteria
August 2, 2016
First Posted (Estimate)
August 5, 2016
Study Record Updates
Last Update Posted (Estimate)
August 5, 2016
Last Update Submitted That Met QC Criteria
August 2, 2016
Last Verified
July 1, 2016
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- RC12_3681 - 5325
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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