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Qualitative Assessment of Implementing Routine Rapid HIV Testing

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00680862
First Posted: May 20, 2008
Last Update Posted: September 29, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
VA Office of Research and Development
  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:


Further study details as provided by VA Office of Research and Development:

Primary Outcome Measures:
  • Number of Participants Who Completed the Survey [ Time Frame: 6 months ]
    survey responses from participants on thoughts pertaining to implementation of HIV rapid testing


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

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
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
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): 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
VA Office of Research and Development
Investigators
Principal Investigator: Henry Anaya, PhD MA VA Greater Los Angeles Healthcare System, West Los Angeles, CA
  More Information

Publications:
Responsible Party: VA Office of Research and Development
ClinicalTrials.gov Identifier: NCT00680862     History of Changes
Other Study ID Numbers: SHP 08-158
First Submitted: May 15, 2008
First Posted: May 20, 2008
Results First Submitted: August 27, 2014
Results First Posted: September 29, 2014
Last Update Posted: September 29, 2014
Last Verified: September 2014

Keywords provided by VA Office of Research and Development:
HIV
screening

Additional relevant MeSH terms:
HIV Infections
Lentivirus Infections
Retroviridae Infections
RNA Virus Infections
Virus Diseases
Sexually Transmitted Diseases, Viral
Sexually Transmitted Diseases
Immunologic Deficiency Syndromes
Immune System Diseases


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