Improving HIV Screening With Nurse-Based Rapid Testing/Streamlined Counseling

NCT00119548 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 251

Last updated 2015-04-07

No results posted yet for this study

Summary

Background: HIV testing is cost-effective in unselected general medical populations, yet testing rates among those at-risk remain low, even among those with regular primary care. HIV rapid testing is effective in many healthcare settings but scant research has been done within primary care settings, nor within the US Department of Veteran's Affairs Healthcare System.

Objectives: We evaluated three methods proven effective in other diseases/settings: Nurse standing orders for testing, streamlined counseling, and HIV rapid testing.

Design: Randomized, controlled trial with three intervention models: Model A (traditional counseling/testing); Model B (nurse-initiated screening, traditional counseling/testing); Model C (nurse-initiated screening, streamlined counseling/rapid testing).

Participants: 251 patients with primary/urgent care appointments in two VA clinics in the same city (one large urban hospital, one freestanding outpatient clinic in a high HIV prevalence area)

Measurements: Rates of HIV testing and receipt of results; sexual risk reduction; HIV knowledge improvement.

Results: Testing rates were 40.2% (Model A), 84.5% (Model B), and 89.3% (Model C) (p=\<.01). Test receipt rates were 14.6% (Model A), 31.0% (Model B), 79.8% (Model C) (all p=\<.01). Sexual risk reduction and knowledge improvement did not differ significantly between counseling methods.

Conclusions: Streamlined counseling with rapid testing significantly increased testing and receipt rates over current practice without changes in risk behavior or post-test knowledge. Increased testing and receipt of results could lead to earlier disease identification, increased treatment and reduced morbidity/mortality. Policymakers should consider streamlined counseling/rapid testing when implementing routine HIV testing into primary/urgent care.

Conditions

  • Health Care Quality, Access, and Evaluation
  • Delivery of Health Care
  • Immune System Diseases
  • HIV Infections

Interventions

OTHER

Rates of HIV testing and receipt of results

Rates of HIV testing and receipt of results

OTHER

Sexual risk reduction; HIV knowledge improvement

Sexual risk reduction; HIV knowledge improvement

OTHER

Rates of HIV testing and receipt of results

Rates of HIV testing and receipt of results

OTHER

Sexual risk reduction; HIV knowledge improvement

Sexual risk reduction; HIV knowledge improvement

OTHER

Rates of HIV testing and receipt of results

Rates of HIV testing and receipt of results

OTHER

Sexual risk reduction; HIV knowledge improvement

Sexual risk reduction; HIV knowledge improvement

Sponsors & Collaborators

Principal Investigators

  • Steven M. Asch, MD MPH · VA Greater Los Angeles Healthcare System, West Los Angeles, CA

  • Douglas K. Owens, MD MS · VA Palo Alto Health Care System, Palo Alto, CA

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2005-03-31
Primary Completion
2007-01-31
Completion
2007-01-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00119548 on ClinicalTrials.gov