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NCT01118195 Clinical Trial

Executive Dysfunction & Suicide: An Exploration Of Risk Factors In Traumatically Brain Injured Veterans

Traumatic Brain Injury (TBI) Clinical Trial

Official title:
Executive Dysfunction & Suicide: An Exploration Of Risk Factors In Traumatically Brain Injured Veterans

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01118195
Other study ID # VA 05-1100
Secondary ID
Status Completed
Phase N/A
First received May 4, 2010
Last updated April 21, 2011
Start date January 2007
Est. completion date April 2011

Study information
Verified date April 2011
Source VA Eastern Colorado Health Care System
Contact n/a
Is FDA regulated No
Health authority United States: Federal GovernmentUnited States: Institutional Review Board
Study type Observational

Clinical Trial Summary

This is a study to learn more about traumatic brain injury (TBI) and suicidal behaviors. The purpose of this research is to find out more about the issues related to these conditions. This study seeks to explore the relationship between executive dysfunction and suicidal behavior in an outpatient population.

Recruitment information / eligibility
Status Completed
Enrollment 54
Est. completion date April 2011
Est. primary completion date April 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 74 Years
Eligibility Inclusion Criteria:

1. Diagnosis of traumatic brain injury, history of suicidal behavior.

2. Age 18-74.

3. Currently receiving care through the Eastern Colorado Health Care System (ECHCS) Denver VA TBI Interdisciplinary Team.

Exclusion Criteria:

1. History of other significant neurological disease.

2. Diagnosis of Schizophrenia.

3. Test of Memory Malingering (TOMM) performance lower than 50%.

4. Behavior which could be described as Substance Abuse in the 7 days prior to participation.

5. Current guardianship or mention of recommendation for guardianship in medical chart within the past six months.

6. Inability to read the informed consent document.

7. Inability to adequately respond to questions regarding the informed consent procedure.

8. Significant hearing impairment.

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
VA Eastern Colorado Health Care System
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