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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01502319
Other study ID # COMIRB 11-0304
Secondary ID
Status Completed
Phase N/A
First received December 9, 2011
Last updated October 18, 2017
Start date September 2010
Est. completion date September 2017

Study information

Verified date October 2017
Source VA Eastern Colorado Health Care System
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

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.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Cognitive therapy
Interventional studies conducted by the consortium focus on a range of cognitive and cognitive-behavioral techniques including cognitive therapy.

Locations

Country Name City State
United States Denver VA Medical Center Denver Colorado

Sponsors (2)

Lead Sponsor Collaborator
VA Eastern Colorado Health Care System United States Department of Defense

Country where clinical trial is conducted

United States, 

Outcome

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
See also
  Status Clinical Trial Phase
Completed NCT01342809 - Follow up by General Practitioner After Self-poisoning N/A
Completed NCT01826240 - Mindfulness-Based Cognitive Therapy + Safety Planning For Suicidal Behavior Phase 1
Completed NCT01528020 - Collaborative Adolescent Research on Emotions and Suicide N/A