NCT01334476

Brief Summary

The VISN 19 MIRECC is involved in research concerned with suicide prevention in high risk populations (e.g., history of traumatic brain injury, post-traumatic stress disorder); Recruitment for future studies will continue with a similar focus. The aim of this protocol is for the VISN 19 MIRECC Research Database (V19-MRD), to have a data repository of participants for possible recruitment from other studies being conducted at the VISN 19 MIRECC. The VISN 19 MIRECC conducts numerous research projects under the review of COMIRB and the VA R\&D.

Trial Health

57
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
5,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jun 2010

Longer than P75 for all trials

Geographic Reach
1 country

2 active sites

Status
recruiting

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

June 1, 2010

Completed
10 months until next milestone

First Submitted

Initial submission to the registry

April 11, 2011

Completed
2 days until next milestone

First Posted

Study publicly available on registry

April 13, 2011

Completed
14.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2026

Completed
Last Updated

April 18, 2025

Status Verified

April 1, 2025

Enrollment Period

15.8 years

First QC Date

April 11, 2011

Last Update Submit

April 16, 2025

Conditions

Demographic DataHistory of Medical and Mental HealthHistory of Combat ExperienceHistory of SuicideImaging Results

Keywords

Data RepositoryFacilitate Recruitment of Participants for Ongoing and Future Research

Outcome Measures

Primary Outcomes (1)

  • Permission to contact for future studies

    One time

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Receiving Medical Treatment at the Denver VA Medical Center 18 or older

You may qualify if:

  • Being a Patient at the Denver VA Medical Center
  • years or Older
  • Participated in another study at the VISN 19 MIRECC

You may not qualify if:

  • Not a Patient at the Denver VA Medical Center
  • Younger than 18 years
  • Never Participated on a Study Within the VISN 19 MIRECC

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

VA Eastern Colorado Health Care System

Denver, Colorado, 80220, United States

RECRUITING

VHAECH Denver VA Medical Center

Denver, Colorado, 80220, United States

RECRUITING

MeSH Terms

Conditions

Psychological Well-Being

Condition Hierarchy (Ancestors)

Personal SatisfactionBehavior

Study Officials

  • Lisa Brenner, PhD

    VA ECHCS

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Lisa Brenner, PhD

CONTACT

(303) 399-8020Lisa.Brenner@va.gov

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
OTHER
Sponsor Type
FED
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Director of the VHA Rocky Mountain MIRECC

Study Record Dates

First Submitted

April 11, 2011

First Posted

April 13, 2011

Study Start

June 1, 2010

Primary Completion

March 1, 2026

Study Completion

March 1, 2026

Last Updated

April 18, 2025

Record last verified: 2025-04

Locations

US(2)