Suicide Clinical Trial
— CASSIOfficial title:
Clinician Access to Soldier Suicide Information (CASSI)
Verified date | October 2017 |
Source | VA Eastern Colorado Health Care System |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The overall objective of this project is to conduct a feasibility study using data proved by Department of Defense National Center for Telehealth and Technology (T2) toward the ultimate goal of establishing a mechanism by which VA clinicians could access data on Veterans regarding suicidal thoughts and/or behaviors that occurred when they were on active duty, as documented in the Department of Defense Suicide Event Report (DoDSER).
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | December 2011 |
Est. primary completion date | December 2011 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 64 Years |
Eligibility |
Inclusion Criteria: - Identified with a history of suicidal thoughts and/or behaviors, as recorded in the Army DoDSER Exclusion Criteria: - Death by suicide contained in the Army DoDSER (i.e., this information will not be sent to us by T2) |
Country | Name | City | State |
---|---|---|---|
United States | VISN 19 Mental Illness Research Education and Clinical Center | Denver | Colorado |
Lead Sponsor | Collaborator |
---|---|
VA Eastern Colorado Health Care System |
United States,
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---|---|---|---|
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