HIV Clinical Trial
Official title:
Multicenter Randomized Controlled Trial Evaluating the Efficacy of HIV/STD Prevention Counseling and Testing in Preventing High Risk Behaviors and New Sexually Transmitted Diseases (Project RESPECT)
The efficacy of counseling to prevent infection with the human immunodeficiency virus (HIV)
and other sexually transmitted diseases (STDs) has not been definitively shown. This
multi-center randomized controlled trial (Project RESPECT) sought to compare the effects of
2 interactive HIV/STD counseling interventions with didactic prevention messages typical of
current practice.
A total of 5758 STD clinic patients were enrolled from 5 public STD clinics (Baltimore, Md;
Denver, Colo; Long Beach, Calif; Newark, NJ; and San Francisco, Calif) between July 1993 and
September 1996. Eligible participants were heterosexual, HIV-negative patients aged 14 years
or older who came for full STD examinations. Using a block design, participating men and
women were randomzied separately to 1 of 3 individual face-to-face interventions. Arm 1
received "enhanced counseling" consisting of 4 interactive counseling sessions based on the
Theory of Reasoned Action and Health Belief Model. Arm 2 received "brief counseling",
consisting of 2 interactive risk-reduction sessions based on CDC's client-centered
counseling model. Arms 3 and 4 each received 2 brief didactic messages about HIV/STD
prevention messages typical of current care at that time. Participants assigned to Arms 1,
2, and 3 were actively followed up after enrollment with questionnaires at 3, 6, 9, and 12
months and STD laboratory examinations and tests at 6 and 12 months. An intent-to-treat
analysis was used to compare interventions. Arm 4 participants were followed passively to
determine potential effects of active study follow-up.
The main outcome measures were self-reported condom use and new diagnoses of STDs
(gonorrhea, chlamydia, syphilis, HIV) defined by laboratory tests.
Results: At the 3- and 6-month follow-up visits, self-reported 100% condom use was higher
(P<.05) in both the enhanced counseling and brief counseling arms compared with participants
in the didactic messages arm. Through the 6-month interval, 30% fewer participants had new
STDs in both the enhanced counseling (7.2%; P = .002) and brief counseling (7.3%;P=.005)
arms compared with those in the didactic messages arm (10.4%). Through the 12-month study,
20% fewer participants in each counseling intervention had new STDs compared with those in
the didactic messages arm (P = .008). Consistently at each of the 5 study sites, STD
incidence was lower in the counseling intervention arms than in the didactic messages
intervention arm. Reduction of STD was similar for men and women and greater for adolescents
and persons with an STD diagnosed at enrollment.
Subset analyses found that
Based on these results, we conclude that short counseling interventions using personalized
risk reduction plans can increase condom use and prevent new STDs. Effective counseling can
be conducted even in busy public clinics.
Status | Completed |
Enrollment | 6000 |
Est. completion date | July 2005 |
Est. primary completion date | |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 14 Years and older |
Eligibility |
Inclusion Criteria: - patients who came to the STD clinic and who were eligible in routine clinic practice to undergo confidential HIV testing Exclusion Criteria: - residence outside the clinics' catchment areas - had made firm plans (e.g., can give a new address) to move outside the clinic catchment area during the next 12 months - unable to provide informed consent to be tested for HIV and take part in the follow up aspect of the study (e.g., incarcerated, mental status changes from drugs, alcohol, medication) - reported that he or she had tested positive for HIV in the past - did not speak and comprehend English well enough to participate in the interventions - came to the clinic for something other than a full routine STD clinic examinations - was a man who reported sex with a man in the past 12 months - had been approached for study participation on a previous clinic visit, and hd already enrolled or refused participation - age < 14 years. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind, Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Centers for Disease Control and Prevention | Baltimore City Health Department, City of Long Beach Department of Health and Human Services, City of Newark Health Department, Colorado Department of Public Health and Environment, San Francisco Department of Public Health |
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