Trial record 9 of 93 for:    Open Studies | "Self-Injurious Behavior"

Operation Worth Living Project With Suicidal Soldiers at Ft. Stewart (OWL)

This study is currently recruiting participants.
Verified May 2012 by The Catholic University of America
Sponsor:
Collaborators:
University of Washington
Information provided by (Responsible Party):
David A. Jobes, Ph.D., The Catholic University of America
ClinicalTrials.gov Identifier:
NCT01300169
First received: February 17, 2011
Last updated: May 15, 2012
Last verified: May 2012
  Purpose

This is a randomized clinical trial comparing the use of new psychotherapy intervention (the "Collaborative Assessment and Management of Suicidality--CAMS") versus enhanced care as usual for suicidal Soldiers who are seen at an outpatient mental health clinic at Ft. Stewart GA.


Condition Intervention
Suicidal Ideation Active
Suicidal and Self-injurious Behavior
Behavioral: The Collaborative Assessment and Management of Suicidality
Behavioral: Enhanced Care as Usual

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: Double Blind (Subject, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: A Randomized Clinical Trial of the Collaborative Assessment and Management of Suicidality Versus Enhanced Care as Usual for Suicidal Soldiers

Resource links provided by NLM:


Further study details as provided by The Catholic University of America:

Primary Outcome Measures:
  • Scale for Suicidal Ideation [ Time Frame: SSI changes from baseline, to post-treatment, and at 1, 3, 6, 12 months follow up ] [ Designated as safety issue: Yes ]
    Industry standard for self-report suicidal ideation


Secondary Outcome Measures:
  • Overall symptom distress [ Time Frame: Baseline, post treatment, 1, 3, 6, 12 months ] [ Designated as safety issue: Yes ]
    Outcome Questionnaire-45


Estimated Enrollment: 150
Study Start Date: March 2011
Estimated Study Completion Date: February 2015
Estimated Primary Completion Date: August 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: CAMS
Collaborative assessment and treatments that target problems that lead to suicidal thinking and behavior.
Behavioral: The Collaborative Assessment and Management of Suicidality
Intensive outpatient, suicide-focused, psychotherapy designed to target and treat the "drivers" of suicidal ideation and behaviors.
Active Comparator: Enhanced Care as Usual
This control group treatment will reflect current clinical practices for treating suicidal soldiers in the research site setting
Behavioral: Enhanced Care as Usual
This is just standard outpatient mental health care that is routinely provided in the study site outpatient clinic

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Active duty Army personnel at FSGA
  • Significant suicidal ideation
  • Soldier is appropriate under FSGA policies
  • Consent at baseline and follow up
  • Consent to randomization and being digitally recorded

Exclusion Criteria:

  • Significant psychosis, cognitive or physical impairment to not give consent
  • Judicially ordered treatments
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01300169

Contacts
Contact: Bradley A. Singer, MSW 912-767-8888 Bradley.Singer@us.army.mil
Contact: David A. Jobes, Ph.D. 202-319-5761 jobes@cua.edu

Locations
United States, Georgia
Fort Stewart Soldier Resiliency Center Recruiting
Ft. Stewart, Georgia, United States, 31314
Contact: Bradley A Singer, MSW    912-767-8888    Bradley.Singer@us.army.mil   
Contact: McRae Philip, Psy.D.    912-767-7301    Philip.S.McRae@US.ARMY.MIL   
Principal Investigator: Bradley A. Singer, MSW         
Sponsors and Collaborators
The Catholic University of America
University of Washington
Investigators
Principal Investigator: David A. Jobes, Ph.D. The Catholic University of America
  More Information

No publications provided

Responsible Party: David A. Jobes, Ph.D., Professor of Psychology, The Catholic University of America
ClinicalTrials.gov Identifier: NCT01300169     History of Changes
Other Study ID Numbers: CUA-001, 09134002
Study First Received: February 17, 2011
Last Updated: May 15, 2012
Health Authority: United States: Institutional Review Board

Keywords provided by The Catholic University of America:
Suicide
Assessment
Intervention
CAMS

Additional relevant MeSH terms:
Self-Injurious Behavior
Suicidal Ideation
Behavioral Symptoms
Suicide

ClinicalTrials.gov processed this record on April 15, 2014