Overview
The primary objective of this study is to evaluate the efficacy of a program of 6 sessions of Cognitive Behavioural Group Therapy (CBGT) (as compared to 6 sessions of Individual Supportive Therapy (IST)) designed for preventing repeat suicide attempts at 12 months post-psychotherapy in adults admitted to inpatient care for suicide attempts.
Description
The secondary objectives of this study are to assess the efficacy of CBGT on:
- parameters describing the incidence of suicide and repeat suicide attempts, as well as suicide re-attempt free follow-up time,
- long-term changes in suicidal ideation,
- long-term changes in psychiatric symptoms (depression, hope for the future, hospitalization).
Eligibility
Inclusion Criteria:
- The patient has been correctly informed
- The patient must have given his/her informed and signed consent
- The patient must be insured or beneficiary of a health insurance plan
- French speaking adults (18 years or older) freely hospitalized (in centres or via emergency services) for prevention of suicide and who have a medium or high suicide risk score according to a Mini International Neuropsychiatric Interview structured interview
- Presence of suicidal ideation according to the Beck Suicide Ideation Scale (score > 3)
- Prior (or recent) suicide attempt within the last three month
- The patient is able to understand the study and capable of giving his/her informed consent
- The patient is available during the weekly time slots proposed by the investigator
Exclusion Criteria:
- The patient is participating in another study that may interfere with the results or conclusions of this study
- Within the past three months, the patient has participated in another study that may interfere with the results or conclusions of this study
- The patient is in an exclusion period determined by a previous study
- The patient is under judicial protection, or is an adult under guardianship
- The patient refuses to sign the consent, or it is impossible to correctly inform the patient
- Emergency situations preventing proper study conduct
- History of schizophrenia or other psychotic troubles
- Presence of psychotic symptoms at initial interview
- Serious cognitive impairment
- Medical incapacity to participate