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Cognitive Behavioral Therapy for Suicide Attempt
N/A
Waitlist Available
Led By David F Tolin, Ph.D.
Research Sponsored by Hartford Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up assessed on a monthly basis for 6 months follow-up.
Awards & highlights
Study Summary
This trial will compare the efficacy of cognitive behavioral therapy to treatment as usual for inpatient suicide prevention.
Eligible Conditions
- Attempted Suicide
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ assessed at baseline, at completion of inpatient treatment (average of 16 days), and on a monthly basis for 6 months follow-up.
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~assessed at baseline, at completion of inpatient treatment (average of 16 days), and on a monthly basis for 6 months follow-up.
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Number of Readmissions
Change in Suicidal Behavior
Change in Suicidal Ideation/Intent
Side effects data
From 2021 Phase 4 trial • 12 Patients • NCT041359378%
irritability
100%
80%
60%
40%
20%
0%
Study treatment Arm
MESH
Trial Design
4Treatment groups
Experimental Treatment
Active Control
Group I: Presence of SUD with BCBTExperimental Treatment1 Intervention
Patients diagnosed with SUD who are randomly assigned to receive BCBT will participate in all aspects of their prescribed treatment plan (i.e., TAU) and will receive up to 4 sessions of CBT (depending on length of stay), lasting 1.5 hours for the first session and 1 hour for the remaining sessions.
Group II: Absence of SUD with BCBTExperimental Treatment1 Intervention
Patients without SUD who are randomly assigned to receive BCBT will participate in all aspects of their prescribed treatment plan (i.e., TAU) and will receive up to 4 sessions of BCBT (depending on length of stay), lasting 1.5 hours for the first session and 1 hour for the remaining sessions.
Group III: Absence of SUD with TAUActive Control1 Intervention
Patients without SUD who are randomly assigned to receive TAU will participate in all aspects of the prescribed treatment plan given by the inpatient unit.
Group IV: Presence of SUD with TAUActive Control1 Intervention
Patients diagnosed with SUD who are randomly assigned to receive TAU will participate in all aspects of the prescribed treatment plan given by the inpatient unit.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Cognitive Behavioral Therapy
2016
Completed Phase 4
~3120
Find a Location
Who is running the clinical trial?
American Foundation for Suicide PreventionOTHER
33 Previous Clinical Trials
9,562 Total Patients Enrolled
Hartford HospitalLead Sponsor
133 Previous Clinical Trials
18,719 Total Patients Enrolled
David F Tolin, Ph.D.Principal InvestigatorInstitute of Living/Hartford Hospital
2 Previous Clinical Trials
136 Total Patients Enrolled
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