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

This study is ongoing, but not recruiting participants.
Sponsor:
Collaborator:
Butler Hospital
Information provided by (Responsible Party):
Shirley Yen, Brown University
ClinicalTrials.gov Identifier:
NCT01748760
First received: December 11, 2012
Last updated: May 1, 2014
Last verified: May 2014
  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: September 2014
Estimated Primary Completion Date: September 2014 (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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01748760

Locations
United States, Rhode Island
Butler Hospital
Providence, Rhode Island, United States, 02906
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: May 1, 2014
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 August 21, 2014