Suicidal and Self-injurious Behaviour Clinical Trial
— MSRCOfficial title:
Military Suicide Research Consortium
Verified date | October 2017 |
Source | VA Eastern Colorado Health Care System |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
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.
Status | Completed |
Enrollment | 5400 |
Est. completion date | September 2017 |
Est. primary completion date | September 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 17 Years and older |
Eligibility |
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. |
Country | Name | City | State |
---|---|---|---|
United States | Denver VA Medical Center | Denver | Colorado |
Lead Sponsor | Collaborator |
---|---|
VA Eastern Colorado Health Care System | United States Department of Defense |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Suicide | Specific outcomes related to suicide will vary as a function of the individual studies conducted within the consortium | varies by study | |
Secondary | Suicide | Secondary outcomes related to suicide will vary as a function of the individual studies conducted within the consortium. | varies by study |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
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|
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Completed |
NCT01826240 -
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Phase 1 | |
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Collaborative Adolescent Research on Emotions and Suicide
|
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