Program to Promote Engagement in Care for the Prevention of Recidivism
NCT ID: NCT04366466
Last Updated: 2020-04-30
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
138 participants
INTERVENTIONAL
2020-05-31
2021-09-30
Brief Summary
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To day, no study has compared the approaches to health surveillance and case management in a clinical trial, nor established the benefit of each on commitment to care and beyond the prevention of suicidal recurrence.
Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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suicide attempt patient who will receive sanitory supervision
The control group will establish the health monitoring
suicide attempt patient using PEPS Program
The research protocol consists of two phases separated by randomization.
A Hospital Phase common to both groups:
Day zero is the day of the suicide attempt for which the patient came to the hospital.
A post-hospital phase including the P.E.P.S. program for the intervention group and telephone reminders for the usual treatment group.
Suicide attempt patient who will participate to PEPS Program
The intervention group will test the program of Promotion of Commitment to Care for the Prevention of Suicidal Recidivism.
suicide attempt patient using PEPS Program
The research protocol consists of two phases separated by randomization.
A Hospital Phase common to both groups:
Day zero is the day of the suicide attempt for which the patient came to the hospital.
A post-hospital phase including the P.E.P.S. program for the intervention group and telephone reminders for the usual treatment group.
Interventions
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suicide attempt patient using PEPS Program
The research protocol consists of two phases separated by randomization.
A Hospital Phase common to both groups:
Day zero is the day of the suicide attempt for which the patient came to the hospital.
A post-hospital phase including the P.E.P.S. program for the intervention group and telephone reminders for the usual treatment group.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Male and female.
* Admission to CH St Denis for a suicide attempt.
* Referral for outpatient follow-up.
* Patient with no psychiatric follow-up or who has been out of follow-up for at least three months.
* Patient having given their written informed consent.
Exclusion Criteria
* Patients who do not have the required faculties to be evaluated (cognitive and delusional disorders).
* Patients treated for more than 72 hours after their procedure (maximum length of stay in the UAS and/or in medical intensive care.
* Patient currently under psychiatric care.
* Patients who cannot be called back by telephone (no telephone, homeless, incarceration).
* Patients who do not master the French language.
18 Years
ALL
No
Sponsors
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Januel
OTHER
Responsible Party
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Januel
Head of clinical research unit
Principal Investigators
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Fayçal MOUAFFAK
Role: PRINCIPAL_INVESTIGATOR
Investigateur Principal
Central Contacts
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References
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Witt KG, Hetrick SE, Rajaram G, Hazell P, Taylor Salisbury TL, Townsend E, Hawton K. Psychosocial interventions for self-harm in adults. Cochrane Database Syst Rev. 2021 Apr 22;4(4):CD013668. doi: 10.1002/14651858.CD013668.pub2.
Other Identifiers
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10477M-PEPS
Identifier Type: -
Identifier Source: org_study_id