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Clinical Trials/NCT01502319
NCT01502319CompletedNot Applicable

Military Suicide Research Consortium

VA Eastern Colorado Health Care System1 site in 1 country5,400 target enrollmentStarted: September 2010Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
5,400
Locations
1
Primary Endpoint
Suicide

Study Overview

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.

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
Observational Model
Other
Time Perspective
Other

Eligibility Criteria

Ages
17 Years to — (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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.

Outcomes

Primary Outcomes

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 Outcomes

  • Suicide(varies by study)

Investigators

Sponsor Class
Fed
Responsible Party
Sponsor

Study Sites (1)

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