Operation Worth Living Project With Suicidal Soldiers at Ft. Stewart (OWL)
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|ClinicalTrials.gov Identifier: NCT01300169|
Recruitment Status : Completed
First Posted : February 21, 2011
Last Update Posted : May 31, 2017
|Condition or disease||Intervention/treatment||Phase|
|Suicidal Ideation Active Suicidal and Self-injurious Behavior||Behavioral: The Collaborative Assessment and Management of Suicidality Behavioral: Enhanced Care as Usual||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||150 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||Double (Participant, Outcomes Assessor)|
|Official Title:||A Randomized Clinical Trial of the Collaborative Assessment and Management of Suicidality Versus Enhanced Care as Usual for Suicidal Soldiers|
|Study Start Date :||March 2011|
|Actual Primary Completion Date :||March 15, 2017|
|Actual Study Completion Date :||March 15, 2017|
Experimental: CAMS--Collaborative Driver-Treatment
The Collaborative Assessment and Management of Suicidality (CAMS) is a suicide-specific clinical intervention that targets and treats patient-defined suicidal "drivers" over the course of clinical care.
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--E-CAU
This control group treatment will reflect current clinical practices for treating suicidal soldiers in the research site setting. These are providers were on site clinicians who provided care according to their usual and customary practices for working with suicidal risk within outpatient care.
Behavioral: Enhanced Care as Usual
This is just standard outpatient mental health care that is routinely provided in the study site outpatient clinic
- Scale for Suicidal Ideation [ Time Frame: Baseline, post-treatment, 1, 3, 6, 12 months ]Industry standard for self-report suicidal ideation
- Overall symptom distress [ Time Frame: Baseline, post treatment, 1, 3, 6, 12 months ]Outcome Questionnaire-45
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01300169
|Principal Investigator:||David A. Jobes, Ph.D.||The Catholic University of America|