Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
2000 participants
OBSERVATIONAL
2010-05-31
2018-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Brief Telehealth Cognitive Rehabilitation Following Mild TBI
NCT05315453
An Innovative Supportive Care Model for Dementia and Traumatic Brain Injury
NCT04495686
Evaluation of VA's Traumatic Brain Injury (TBI) Clinical Reminder and Comprehensive TBI Evaluation (CTBIE)
NCT00852527
Cognitive-Communication Screening and Early Therapy for Adults With Mild TBI
NCT03230656
Executive Dysfunction and Self-Harm Behavior: An Examination of Veterans With TBI, PTSD, or Both
NCT01334463
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
1. Establishing the criterion-related validity of the Traumatic Brain Injury-4 (TBI-4) questionnaire in the Veteran homeless population using the Ohio State University TBI-Identification Method (OSU TBI-ID) (Corrigan et al., 2007) as the gold standard for establishing traumatic brain injury (TBI) diagnosis.
2. Identifying the prevalence of those that screen positive for a lifetime history of TBI among homeless Veterans.
3. Comparing psychiatric outcomes (psychiatric hospitalizations, suicide attempts and deaths, and clinical contacts) and psychosocial outcomes between those with and without a lifetime history of TBI.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
CROSS_SECTIONAL
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
18 Years
89 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
US Department of Veterans Affairs
FED
Corporal Michael J. Crescenz VA Medical Center
FED
James A. Haley Veterans Administration Hospital
FED
VA Eastern Colorado Health Care System
FED
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Lisa Brenner
Director, VISN 19 MIRECC
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Lisa A. Brenner, Ph. D.
Role: PRINCIPAL_INVESTIGATOR
VISN 19 MIRECC
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Department of Veterans Affairs, Eastern Colorado Health Care System
Denver, Colorado, United States
Tampa VAMC
Tampa, Florida, United States
Philadelphia VAMC
Philadelphia, Pennsylvania, United States
Countries
Review the countries where the study has at least one active or historical site.
Related Links
Access external resources that provide additional context or updates about the study.
MIRECC Web Site
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
10-0170
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.