Coping Long Term With Attempted Suicide - Adolescents (CLASP-A)
This study is currently recruiting participants.
Verified December 2012 by Brown University
Sponsor:
Brown University
Collaborator:
Butler Hospital
Information provided by (Responsible Party):
Shirley Yen, Brown University
ClinicalTrials.gov Identifier:
NCT01748760
First received: December 11, 2012
Last updated: December 12, 2012
Last verified: December 2012
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Purpose
This study is to develop an adjunctive intervention for acutely suicidal adolescents who have been admitted to a psychiatric inpatient unit. The study intervention is comprised of: 1) two individual sessions delivered in an inpatient setting or immediately upon discharge; 2) one family session; 3) six months of follow-up phone interventions. The investigators hypothesize that those who receive the study intervention will have lower rates of suicide events and greater decreases in suicidal ideation after six months.
| Condition | Intervention |
|---|---|
|
Suicide |
Behavioral: CLASP-A intervention Other: Treatment as Usual |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Single Blind (Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | Coping Long Term With Attempted Suicide - Adolescents |
Resource links provided by NLM:
Further study details as provided by Brown University:
Primary Outcome Measures:
- Suicide events [ Time Frame: 6 months ] [ Designated as safety issue: No ]Suicide attempts (actual, aborted, interrupted) or emergency interventions to intercede an attempt.
| Estimated Enrollment: | 50 |
| Study Start Date: | October 2012 |
| Estimated Study Completion Date: | December 2013 |
| Estimated Primary Completion Date: | December 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: CLASP-A intervention
Adolescent participants and parents will receive adjunctive psychosocial intervention.
|
Behavioral: CLASP-A intervention |
|
Active Comparator: Treatment as Usual
Adolescent participants and parents will not receive study intervention
|
Other: Treatment as Usual |
Eligibility| Ages Eligible for Study: | 12 Years to 18 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Admission to an inpatient unit due to suicide risk
- English speaking
Exclusion Criteria:
- Active psychosis
- Cognitive Disability
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01748760
Contacts
| Contact: Shirley Yen, Ph.D. | 4014441915 | Shirley_Yen_PhD@Brown.edu |
Locations
| United States, Rhode Island | |
| Butler Hospital | Recruiting |
| Providence, Rhode Island, United States, 02906 | |
| Contact: Shirley Yen, Ph.D. 401-444-1915 Shirley_Yen_PhD@Brown.edu | |
Sponsors and Collaborators
Brown University
Butler Hospital
Investigators
| Principal Investigator: | Shirley Yen, Ph.D. | Brown University |
More Information
No publications provided
| Responsible Party: | Shirley Yen, Assistant Professor (Research), Brown University |
| ClinicalTrials.gov Identifier: | NCT01748760 History of Changes |
| Other Study ID Numbers: | R34 MH090147 |
| Study First Received: | December 11, 2012 |
| Last Updated: | December 12, 2012 |
| Health Authority: | United States: Federal Government |
Keywords provided by Brown University:
|
Suicide Attempts Suicidal Ideation |
Additional relevant MeSH terms:
|
Suicide Suicide, Attempted Self-Injurious Behavior Behavioral Symptoms |
ClinicalTrials.gov processed this record on May 23, 2013