Working...
ClinicalTrials.gov
ClinicalTrials.gov Menu

Qualitative Assessment of Implementing Routine Rapid HIV Testing

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.
ClinicalTrials.gov Identifier: NCT00680862
Recruitment Status : Completed
First Posted : May 20, 2008
Results First Posted : September 29, 2014
Last Update Posted : September 29, 2014
Sponsor:
Information provided by (Responsible Party):
VA Office of Research and Development ( US Department of Veterans Affairs )

Study Type Observational
Study Design Observational Model: Cohort;   Time Perspective: Cross-Sectional
Condition HIV Infections
Enrollment 25
Recruitment Details  
Pre-assignment Details  
Arm/Group Title Group 1
Hide Arm/Group Description VA employees
Period Title: Overall Study
Started 25
Completed 25
Not Completed 0
Arm/Group Title Group 1
Hide Arm/Group Description VA employees
Overall Number of Baseline Participants 25
Hide Baseline Analysis Population Description
VA employees
Age, Continuous  
Mean (Standard Deviation)
Unit of measure:  Years
Number Analyzed 25 participants
36  (2)
Age, Categorical  
Measure Type: Count of Participants
Unit of measure:  Participants
Number Analyzed 25 participants
<=18 years
0
   0.0%
Between 18 and 65 years
25
 100.0%
>=65 years
0
   0.0%
Sex: Female, Male  
Measure Type: Count of Participants
Unit of measure:  Participants
Number Analyzed 25 participants
Female
0
   0.0%
Male
25
 100.0%
Region of Enrollment  
Measure Type: Number
Unit of measure:  Participants
United States Number Analyzed 25 participants
25
1.Primary Outcome
Title Number of Participants Who Completed the Survey
Hide Description survey responses from participants on thoughts pertaining to implementation of HIV rapid testing
Time Frame 6 months
Hide Outcome Measure Data
Hide Analysis Population Description
[Not Specified]
Arm/Group Title Group 1
Hide Arm/Group Description:
VA employees
Overall Number of Participants Analyzed 25
Measure Type: Number
Unit of Measure: participants
25
Time Frame [Not Specified]
Adverse Event Reporting Description Serious and other [non-serious] adverse events were not collected or assessed as part of the study
 
Arm/Group Title Group 1
Hide Arm/Group Description VA employees
All-Cause Mortality
Group 1
Affected / at Risk (%)
Total   --/-- 
Show Serious Adverse Events Hide Serious Adverse Events
Group 1
Affected / at Risk (%)
Total   0/0 
Show Other (Not Including Serious) Adverse Events Hide Other (Not Including Serious) Adverse Events
Frequency Threshold for Reporting Other Adverse Events 0%
Group 1
Affected / at Risk (%)
Total   0/0 
Certain Agreements
All Principal Investigators ARE employed by the organization sponsoring the study.
Results Point of Contact
Name/Title: Henry Anaya
Organization: VHA
Phone: 310-478-3711 ext 48488
Responsible Party: VA Office of Research and Development ( US Department of Veterans Affairs )
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