Clinical Trials Directory

Trials / Recruiting

RecruitingNCT01334476

VISN 19 MIRECC Research Database

Status
Recruiting
Phase
Study type
Observational
Enrollment
5,000 (estimated)
Sponsor
VA Eastern Colorado Health Care System · Federal
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed description

This protocol seeks to formally create the database that will store demographic data. The data will be used by VISN 19 MIRECC Investigators solely for recruitment purposes for future studies. The repository data will include: 1. Data regarding individuals in existing study databases who have already provided permission to have their information stored and used for future recruitment into VISN 19 MIRECC research studies (specific data elements to be collected will be articulated below). 2. Data of individuals to be collected and saved to use for future recruitment into VISN 19 MIRECC research studies. A restricted section of the V19-MRD will contain V19-MRD identification numbers and identifying data including name (first, last, middle initial), Social Security number, phone number(s) (primary and secondary), date of birth, and mailing address. A less restricted section of the V19-MRD will contain V19-MRD identification numbers, the COMIRB protocol number of the study the participant was recruited from, gender, year of birth, and criteria identifiers marked as present or absent (i.e., history of medical and mental health conditions, history of suicide - thoughts/behaviors, history of combat experience, and presence of imaging results). The V19-MRD would enhance current research strategies by first allowing VISN 19 MIRECC Investigators an efficient method to conduct preliminary or ongoing investigations to determine if: 1) sufficient populations exist to conduct a study; or 2) potential participants meeting specific study criteria are included in the database who could be contacted regarding study participation. Second, with an approved protocol, the V19-MRD contact section of the database could be used to facilitate mailings to potential participants.

Conditions

Timeline

Start date
2010-06-01
Primary completion
2026-03-01
Completion
2026-03-01
First posted
2011-04-13
Last updated
2025-04-18

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01334476. Inclusion in this directory is not an endorsement.