Coping Long Term With Attempted Suicide - Adolescents (CLASP-A)

This study is currently recruiting participants.
Verified December 2012 by Brown University
Sponsor:
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
  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 April 17, 2014