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Clinical Trials/NCT01686750
NCT01686750
Completed
Not Applicable

A Cluster Randomized Trial of Integrated Care Centers to Improve Access to HIV Prevention, Testing, and Treatment Services Among High-Risk Vulnerable Populations in India

Johns Hopkins University1 site in 1 country21,726 target enrollmentStarted: October 2012Last updated:
ConditionsHIV Infection

Overview

Phase
Not Applicable
Status
Completed
Enrollment
21,726
Locations
1
Primary Endpoint
Proportion Reporting HIV Testing in the Prior 12 Months

Overview

Brief Summary

This is a cluster randomized trial to evaluate the effectiveness of integrated care centers (ICC) to improve access to HIV testing, prevention services, and treatment among high-risk populations of injection drug users (IDU) and men who have sex with men (MSM) in India. We will collect baseline ethnographic and survey data from approximately 27 IDU or MSM sites in India. We will use baseline data to select 22 sites for the trial (12 IDU and 10 MSM) and to stratify sites according to key baseline characteristics. We will perform stratified randomization to assign sites to either the ICC intervention or to standard services. ICCs, which will be either IDU or MSM-focused, will provide an accepting atmosphere in which members of vulnerable groups can drop-in, receive rapid HIV voluntary counselling and testing, risk reduction counseling and services, and antiretroviral therapy. ICCs will be scaled-up from existing governmental or non-governmental organizations and services provided at ICCs will be supported by the National AIDS Control Organization (NACO) of India. After providing services in communities for two years, we will conduct an evaluation survey (with biological and behavioral measures) of approximately 1000 subjects in the target populations in each of the 22 study sites. Integrated care centers have the potential to improve access to HIV prevention and treatment services among vulnerable, high-risk populations.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Key Informant Interviews:
  • Persons may be included in the key informant interviews if they meet all of the following criteria:
  • 18 years of age or older
  • Knowledge of the local HIV risk group of interest (IDU or MSM)
  • Psychologically fit to participate in the study and to understand the consent
  • Ability to comprehend one of the consent translation languages
  • Provide informed consent
  • Focus groups:
  • Persons may be included in the focus groups if they meet all of the following criteria:
  • 18 years of age or older

Exclusion Criteria

  • Key Informant Interviews:
  • Persons will be excluded from the key informant interviews if they meet any of the following criteria:
  • Younger than 18 years
  • Do not have knowledge of the local HIV risk group of interest (IDU or MSM)
  • Are not psychologically fit to participate in the study or to understand the consent
  • Do not have ability to comprehend one of the consent translation languages
  • Do not provide informed consent
  • Focus groups:
  • Persons will be excluded from the focus groups if they meet any of the following criteria:
  • Younger than 18 years

Outcomes

Primary Outcomes

Proportion Reporting HIV Testing in the Prior 12 Months

Time Frame: 2 years

Self-reported HIV testing in the prior 12 months among all survey participants, excluding those who reported being diagnosed with HIV more than 12 months previously.

Secondary Outcomes

  • Proportion of IDU Reporting Drug Abstinence in Prior 6 Months(2 years)
  • Proportion of HIV-infected Participants Visiting an HIV Treatment Provider in Prior 6 Months(2 years)
  • Proportion of IDU Reporting Needle or Syringe Sharing in Prior 6 Months(2 years)
  • Vicarious Stigma as Assessed by 6-item Stigma Scale(2 years)
  • Proportion of HIV-infected Participants Aware of Status(2 years)
  • Community Viral Load(2 years)
  • Proportion of MSM Reporting Unprotected Anal Intercourse With Non-main Partner in Prior 6 Months(2 years)
  • Prevalence of Recent HIV Infection(2 years)
  • Proportion Reporting Spouse Ever Tested for HIV(2 years)
  • Proportion of Antiretroviral Therapy-eligible HIV-infected Participants Using Antiretroviral Therapy(2 years)
  • Proportion of HIV-infected Participants With Suppressed HIV RNA(2 years)
  • Number of Non-main Male Partners in Prior 6 Months in MSM(2 years)
  • Proportion Reporting Substance Abuse Among MSM(2 years)
  • Proportion With Depressive Symptoms(2 years)
  • Number of Unprotected Sexual Acts Reported by MSM(2 years)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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