Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03992105
Other study ID # 2019-33
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date October 1, 2019
Est. completion date October 1, 2020

Study information

Verified date June 2019
Source Assistance Publique Hopitaux De Marseille
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Document the effectiveness of the "Respite Site" program in relation to the current health system. Document in particular the number and type of constraints, lengths of hospitalization and mode of exit, as well as the exit destination of psychotic homeless people.


Description:

Between 2012 and 2015, the practice of "stress-related care" related to crisis situations increased by 15%, with about 90,000 people under duress making France one of the European countries where practice most under stress. Being homeless, from a visible ethnic minority, combined with the lack of alternatives in the territory are well-documented risk factors for being hospitalized under duress. A review of the 2015 literature has shown that out-of-hospital crisis sites achieve results equivalent to those of conventional hospitalization in terms of reduced symptomatology and would have better outcomes in terms of increase in remission and recovery times of professional activity and social inclusion, with greater efficiency. In Marseille, an experimental device has shown its capacity to propose an alternative to hospitalization, for this type of population.Running the lessons of this experiment and inspired by the experimentation Parachute, a new device experimental, called "Place of respite", This place proposes a model of resolution of the psychotic crisis where the person decides the type of care that she wish to receive. It is a device that is therefore an alternative to conventional psychiatric care under duress. The investigators formulate the hypothesis that alternative support to the resolution of the crisis by using the skills of people with disorders severe psychiatric conditions in the experimental "Respite site" decreases in the short term the number of hospitalizations and their duration, as well as the experience of the constraint in the course of care of these people, compared to the subjects who did not benefit from this device and could represent a model of crisis management / psychiatric emergency efficient with regard to the current offer.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 200
Est. completion date October 1, 2020
Est. primary completion date December 30, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

Over 18 years old Diagnosed with schizophrenia, bipolar I disorder, or schizoaffective disorder according to the DSMIV classification Homeless "ETHOS 1 or 2" (FEANTSA classification) In a crisis situation: psychiatric crisis (PANSS increase of more than 20%), social crisis (significant alteration of social relations) Affiliated to a social protection scheme Accepting to participate in the study An HCAT score greater than or equal to 3

Exclusion Criteria:

Under 18 years old Participant in another study simultaneously in accordance with Article L112112 of the public health code Refusing to participate in the study, or whose legal representative refuses to participate in the study in the case of a person under guardianship or curatorship A score on the HCAT scale (decision-making competence) strictly less than 3

Study Design


Related Conditions & MeSH terms


Intervention

Other:
prospective cohort
topics included openly in the "Respite Site", made up of the first 50 subjects followed prospectively

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique Hopitaux De Marseille

Outcome

Type Measure Description Time frame Safety issue
Primary Needs Assessement Scoring the Montreal Assement Need questionnaire 36 months
See also
  Status Clinical Trial Phase
Completed NCT06267534 - Mindfulness-based Mobile Applications Program N/A
Completed NCT04108689 - Internet-based Acceptance and Commitment Training for Elite Ice Hockey Players N/A
Recruiting NCT06012084 - The Development and Evaluation of iCF-PWR for Healthy Siblings of Individuals With Cystic Fibrosis N/A
Completed NCT04085861 - Mental Health in Dancers; an Intervention Study N/A
Recruiting NCT05227352 - Bio-Experiential Spaces for Mental Health in Healthworkers N/A
Completed NCT03663075 - Effect of Group Education and Individual Counselling on Mental Health and Quality of Life in 45-60 Year Old Women N/A
Completed NCT02480907 - Supporting Carers of Children and Adolescents With Eating Disorders in Austria (SUCCEAT) N/A
Completed NCT02157766 - Wisconsin Center for the Neuroscience and Psychophysiology of Meditation N/A
Completed NCT01155687 - Psychosocial Counseling in Afghanistan N/A
Unknown status NCT01177696 - Intervention in Groups of Family Caregivers in Primary Health Care N/A
Completed NCT01037946 - Family to Family: Psychoeducation to Improve Children's Outcomes in HIV+ Families N/A
Completed NCT00700349 - Evaluation of Impacts of Access to Credit and Loan Size for Microcredit Clients in South Africa N/A
Recruiting NCT03885401 - Enhanced Care Planning for Patients With Multiple Chronic Conditions N/A
Completed NCT03118388 - Engaging Homeless Youth in Vocational Training to Meet Their Mental Health Needs Phase 2
Completed NCT05061966 - The Digital Wellbeing Project N/A
Completed NCT04546061 - Project Uplift: Substance Use and Mental Health Treatment for Young Sexual and Gender Minorities N/A
Completed NCT04026308 - Written vs Electronic Safety Planning Study N/A
Completed NCT05738109 - Evaluating the Efficacy of a 91-day Self-talk Mental Health Self-care Journal N/A
Completed NCT03901274 - Partnering for Student Wellness N/A
Not yet recruiting NCT05910580 - Improving Alcohol and Substance Use Care Access, Outcome, Equity During the Reproductive Years N/A