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Military Suicide Research Consortium (MSRC)

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ClinicalTrials.gov Identifier: NCT01502319
Recruitment Status : Completed
First Posted : December 30, 2011
Last Update Posted : October 20, 2017
Information provided by (Responsible Party):

Study Description
Brief Summary:

The Consortium's overall mission can be summarized as follows; each function is developed with the goal of clear military relevance:

  1. Produce new scientific knowledge about suicidal behavior in the military that improves mental health outcomes for the investigators men and women in uniform.
  2. Use high quality research methods and analyses to address problems in policy and practice that have a direct impact on suicide-related and other mental health outcomes for military personnel.
  3. Disseminate Consortium knowledge, information, and findings through a variety of methods appropriate for decision makers, practitioners, and others who are accountable for ensuring the mental health of military personnel. This includes the rapid response function so that queries from decision makers and others to the Consortium are answered with speed and efficiency. Technical assistance and support for decision makers and others is an integral aspect of this Consortium function. This aspect of the Consortium will warehouse knowledge about suicidal behavior in general (e.g., from civilian and international sources as well as from military sources), so that military issues can be informed in a comprehensive manner.
  4. Train future leaders in military suicide research through experience within a multi-disciplinary setting for Ph.D. students and postdoctoral scholars interested in research questions on military suicide of both a basic and applied nature.

Condition or disease Intervention/treatment
Suicidal and Self-injurious Behaviour Behavioral: Cognitive therapy

Detailed Description:
This is a research consortium responsible for the conduct of a wide range of studies, including clinical trials. All clinical trials funded through the consortium will be registered separately.

Study Design

Study Type : Observational
Actual Enrollment : 5400 participants
Observational Model: Other
Time Perspective: Other
Official Title: Military Suicide Research Consortium
Actual Study Start Date : September 2010
Primary Completion Date : September 2017
Study Completion Date : September 2017

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Self-harm Suicide
U.S. FDA Resources

Groups and Cohorts

Group/Cohort Intervention/treatment
All subjects
Group/Cohort label is not applicable to this umbrella protocol. The Consortium funds specific research teams who will determine the number of group(s)/cohort(s) relevant to their study.
Behavioral: Cognitive therapy
Interventional studies conducted by the consortium focus on a range of cognitive and cognitive-behavioral techniques including cognitive therapy.

Outcome Measures

Primary Outcome Measures :
  1. Suicide [ Time Frame: varies by study ]
    Specific outcomes related to suicide will vary as a function of the individual studies conducted within the consortium

Secondary Outcome Measures :
  1. Suicide [ Time Frame: varies by study ]
    Secondary outcomes related to suicide will vary as a function of the individual studies conducted within the consortium.

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   17 Years and older   (Child, Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population
Given the age range of active duty military, reservists, and veterans, it is expected that funded Study Principal Investigators will enroll subjects that are young adults (18 to 21 years) to Senior Citizens (over 65 years).

Inclusion Criteria:

  • MSRC studies are inclusive of all individuals who are eligible as defined by each study's protocol regardless of age, gender, race or ethnicity, socioeconomic status, sexual orientation, and any other demographic characteristics. Measures and treatments are translated and culturally adapted to the extent possible.

Exclusion Criteria:

  • Specific to each investigator's protocol.
Contacts and Locations

Information from the National Library of Medicine

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): NCT01502319

United States, Colorado
Denver VA Medical Center
Denver, Colorado, United States, 80220
Sponsors and Collaborators
VA Eastern Colorado Health Care System
United States Department of Defense
Principal Investigator: Peter M Gutierrez, PhD VA Eastern Colorado Health Care System
More Information

Additional Information:
Responsible Party: VA Eastern Colorado Health Care System
ClinicalTrials.gov Identifier: NCT01502319     History of Changes
Other Study ID Numbers: COMIRB 11-0304
First Posted: December 30, 2011    Key Record Dates
Last Update Posted: October 20, 2017
Last Verified: October 2017

Additional relevant MeSH terms:
Self-Injurious Behavior
Behavioral Symptoms