NCT01502319

Brief Summary

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

  1. 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. 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. 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. 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
5,400

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Sep 2010

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2010

Completed
1.3 years until next milestone

First Submitted

Initial submission to the registry

December 9, 2011

Completed
21 days until next milestone

First Posted

Study publicly available on registry

December 30, 2011

Completed
5.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2017

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2017

Completed
Last Updated

October 20, 2017

Status Verified

October 1, 2017

Enrollment Period

7 years

First QC Date

December 9, 2011

Last Update Submit

October 18, 2017

Conditions

Suicidal and Self-injurious Behaviour

Outcome Measures

Primary Outcomes (1)

  • Suicide

    Specific outcomes related to suicide will vary as a function of the individual studies conducted within the consortium

    varies by study

Secondary Outcomes (1)

  • Suicide

    varies by study

Study Arms (1)

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

Interventions

Cognitive therapyBEHAVIORAL

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

All subjects

Eligibility Criteria

Age17 Years+
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability 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).

You may qualify if:

  • 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.

You may not qualify if:

  • Specific to each investigator's protocol.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Denver VA Medical Center

Denver, Colorado, 80220, United States

Location

Related Links

MeSH Terms

Conditions

Self-Injurious Behavior

Interventions

Cognitive Behavioral Therapy

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehavior

Intervention Hierarchy (Ancestors)

Behavior TherapyPsychotherapyBehavioral Disciplines and Activities

Study Officials

  • Peter M Gutierrez, PhD

    VA Eastern Colorado Health Care System

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
OTHER
Sponsor Type
FED
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 9, 2011

First Posted

December 30, 2011

Study Start

September 1, 2010

Primary Completion

September 1, 2017

Study Completion

September 1, 2017

Last Updated

October 20, 2017

Record last verified: 2017-10

Locations

US(1)