Qualitative Assessment of Implementing Routine Rapid HIV Testing
This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Department of Veterans Affairs
ClinicalTrials.gov Identifier:
NCT00680862
First received: May 15, 2008
Last updated: April 23, 2012
Last verified: October 2008
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Purpose
Qualitative assessment of implementing routine HIV rapid testing in primary care clinics within VA
| Condition |
|---|
|
HIV Infections |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Cross-Sectional |
| Official Title: | Qualitative Assessment of Implementing Routine Rapid HIV Testing |
Resource links provided by NLM:
Genetics Home Reference related topics:
complement factor I deficiency
MedlinePlus related topics:
HIV/AIDS
U.S. FDA Resources
Further study details as provided by Department of Veterans Affairs:
Primary Outcome Measures:
- survey responses [ Time Frame: 6 months ] [ Designated as safety issue: No ]
| Enrollment: | 25 |
| Study Start Date: | June 2008 |
| Study Completion Date: | September 2008 |
| Primary Completion Date: | September 2008 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
|
Group 1
VA employees
|
Show Detailed Description
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Study Population
key informant VA employees
Criteria
Inclusion Criteria:
- VA employees of LA OPC who are involved in HIV care and/or policy
Exclusion Criteria:
- n/a
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00680862
Locations
| United States, California | |
| VA Greater Los Angeles Healthcare System, West Los Angeles, CA | |
| West Los Angeles, California, United States, 90073 | |
Sponsors and Collaborators
Investigators
| Principal Investigator: | Henry Anaya, PhD MA | VA Greater Los Angeles Healthcare System, West Los Angeles, CA |
More Information
No publications provided
| Responsible Party: | Department of Veterans Affairs |
| ClinicalTrials.gov Identifier: | NCT00680862 History of Changes |
| Other Study ID Numbers: | SHP 08-158 |
| Study First Received: | May 15, 2008 |
| Last Updated: | April 23, 2012 |
| Health Authority: | United States: Federal Government |
Keywords provided by Department of Veterans Affairs:
|
HIV screening |
Additional relevant MeSH terms:
|
HIV Infections Acquired Immunodeficiency Syndrome Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases |
Immunologic Deficiency Syndromes Immune System Diseases Slow Virus Diseases HIV Antibodies Immunologic Factors Physiological Effects of Drugs Pharmacologic Actions |
ClinicalTrials.gov processed this record on June 18, 2013