- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01686750
Integrated Care Centers to Improve HIV Outcomes in Vulnerable Indian Populations
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
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Tamil Nadu
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Chennai, Tamil Nadu, India, 600113
- YR Gaitonde Center for AIDS Research and Education
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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
Member of a target HIV risk group, meeting criterion 2a or 2b
- IDU: self-reported injection drug use in prior 12 months
- MSM: self-identify as male and report oral/anal sex with another male in prior 12 months
- Psychologically fit to participate in the study and to understand the consent
- Ability to comprehend one of the consent translation languages
- Provide informed consent
Baseline or evaluation respondent-driven sampling (RDS) survey
Persons may be included in the baseline or evaluation RDS survey if they meet all of the following criteria:
- 18 years of age or older
Member of a target HIV risk group, meeting criterion 2a or 2b
- IDU: self-reported injection drug use in prior 24 months
- MSM: self-identify as male and report oral/anal sex with another male in prior 12 months
- Psychologically fit to participate in the study and to understand the consent
- Ability to comprehend one of the consent translation languages
- Present a valid RDS referral coupon (unless a seed)
- Provide informed consent
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
Are not a member of a target HIV risk group, meeting neither criterion 2a nor 2b
- IDU: self-reported injection drug use in prior 12 months
- MSM: self-identify as male and report oral/anal sex with another male in prior 12 months
- 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
Baseline or evaluation RDS survey
Persons will be excluded in the baseline or evaluation RDS survey if they meet any of the following criteria:
- Younger than 18 years
Are not a member of a target HIV risk group, meeting neither criterion 2a nor 2b
- IDU: self-reported injection drug use in prior 24 months
- MSM: self-identify as male and report oral/anal sex with another male in prior 12 months
- 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 present a valid RDS referral coupon and are not a seed
- Do not provide informed consent
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Integrated care centers
Integrated care centers will provide HIV prevention and treatment services to high risk populations of IDU or MSM in an accepting and supportive environment.
|
|
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No Intervention: Standard services
In Standard Services sites, HIV testing, prevention, and treatment services will be available through standard venues.
Government centers typically provide most HIV testing services and are the only source for free antiretroviral therapy.
Non-governmental organizations typically provide prevention and risk reduction services.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
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.
|
2 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Proportion of HIV-infected Participants Aware of Status
Time Frame: 2 years
|
Proportion of HIV-positive participants that were aware of their status at the time of the visit
|
2 years
|
|
Proportion of HIV-infected Participants Visiting an HIV Treatment Provider in Prior 6 Months
Time Frame: 2 years
|
2 years
|
|
|
Proportion of Antiretroviral Therapy-eligible HIV-infected Participants Using Antiretroviral Therapy
Time Frame: 2 years
|
2 years
|
|
|
Community Viral Load
Time Frame: 2 years
|
Average log(10) HIV RNA concentration among HIV-infected participants
|
2 years
|
|
Proportion of HIV-infected Participants With Suppressed HIV RNA
Time Frame: 2 years
|
Proportion of HIV-positive participants meeting criteria for antiretroviral therapy [cluster of differentiation 4 (CD4) count <350 cells/mm3 or current or past use of antiretroviral therapy)] who have a suppressed viral load (HIV RNA <150 copies/mL)
|
2 years
|
|
Prevalence of Recent HIV Infection
Time Frame: 2 years
|
2 years
|
|
|
Proportion of IDU Reporting Needle or Syringe Sharing in Prior 6 Months
Time Frame: 2 years
|
2 years
|
|
|
Proportion of IDU Reporting Drug Abstinence in Prior 6 Months
Time Frame: 2 years
|
2 years
|
|
|
Proportion of MSM Reporting Unprotected Anal Intercourse With Non-main Partner in Prior 6 Months
Time Frame: 2 years
|
2 years
|
|
|
Number of Non-main Male Partners in Prior 6 Months in MSM
Time Frame: 2 years
|
2 years
|
|
|
Proportion Reporting Substance Abuse Among MSM
Time Frame: 2 years
|
2 years
|
|
|
Proportion With Depressive Symptoms
Time Frame: 2 years
|
Participants with Score >=10 on Patient Health Questionnaire-9
|
2 years
|
|
Number of Unprotected Sexual Acts Reported by MSM
Time Frame: 2 years
|
2 years
|
|
|
Vicarious Stigma as Assessed by 6-item Stigma Scale
Time Frame: 2 years
|
Summed score from a 6-item stigma scale (range 0-18), with higher values indicating more perceived stigma
|
2 years
|
|
Proportion Reporting Spouse Ever Tested for HIV
Time Frame: 2 years
|
2 years
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Shruti Mehta, PhD, Johns Hopkins University
- Principal Investigator: David D Celentano, ScD, Johns Hopkins University
- Principal Investigator: Suniti Solomon, MD, YR Gaitonde Centre for AIDS Research and Education
- Principal Investigator: Aylur Srikrishnan, BA, YR Gaitonde Centre for AIDS Research and Education
- Principal Investigator: Suresh Kumar, MPH, YR Gaitonde Centre for AIDS Research and Education
- Principal Investigator: Sunil S Solomon, PhD, Johns Hopkins University
Publications and helpful links
General Publications
- Solomon SS, Mehta SH, Srikrishnan AK, Vasudevan CK, Mcfall AM, Balakrishnan P, Anand S, Nandagopal P, Ogburn EL, Laeyendecker O, Lucas GM, Solomon S, Celentano DD. High HIV prevalence and incidence among MSM across 12 cities in India. AIDS. 2015 Mar 27;29(6):723-31. doi: 10.1097/QAD.0000000000000602.
- Lucas GM, Solomon SS, Srikrishnan AK, Agrawal A, Iqbal S, Laeyendecker O, McFall AM, Kumar MS, Ogburn EL, Celentano DD, Solomon S, Mehta SH. High HIV burden among people who inject drugs in 15 Indian cities. AIDS. 2015 Mar 13;29(5):619-28. doi: 10.1097/QAD.0000000000000592.
- Solomon SS, Mehta SH, Srikrishnan AK, Solomon S, McFall AM, Laeyendecker O, Celentano DD, Iqbal SH, Anand S, Vasudevan CK, Saravanan S, Lucas GM, Kumar MS, Sulkowski MS, Quinn TC. Burden of hepatitis C virus disease and access to hepatitis C virus services in people who inject drugs in India: a cross-sectional study. Lancet Infect Dis. 2015 Jan;15(1):36-45. doi: 10.1016/S1473-3099(14)71045-X. Epub 2014 Dec 3.
- Solomon SS, Lucas GM, Celentano DD, Sifakis F, Mehta SH. Beyond surveillance: a role for respondent-driven sampling in implementation science. Am J Epidemiol. 2013 Jul 15;178(2):260-7. doi: 10.1093/aje/kws432. Epub 2013 Jun 25.
- Solomon SS, Lucas GM, Celentano DD, McFall AM, Ogburn E, Moulton LH, Srikrishnan AK, Kumar MS, Anand S, Solomon S, Mehta SH. Design of the Indian NCA study (Indian national collaboration on AIDS): a cluster randomized trial to evaluate the effectiveness of integrated care centers to improve HIV outcomes among men who have sex with men and persons who inject drugs in India. BMC Health Serv Res. 2016 Nov 14;16(1):652. doi: 10.1186/s12913-016-1905-5.
- Mehta SH, Lucas GM, Solomon S, Srikrishnan AK, McFall AM, Dhingra N, Nandagopal P, Kumar MS, Celentano DD, Solomon SS. HIV care continuum among men who have sex with men and persons who inject drugs in India: barriers to successful engagement. Clin Infect Dis. 2015 Dec 1;61(11):1732-41. doi: 10.1093/cid/civ669. Epub 2015 Aug 6.
- Solomon SS, Solomon S, McFall AM, Srikrishnan AK, Anand S, Verma V, Vasudevan CK, Balakrishnan P, Ogburn EL, Moulton LH, Kumar MS, Sachdeva KS, Laeyendecker O, Celentano DD, Lucas GM, Mehta SH; Indian National Collaboration on AIDS Study. Integrated HIV testing, prevention, and treatment intervention for key populations in India: a cluster-randomised trial. Lancet HIV. 2019 May;6(5):e283-e296. doi: 10.1016/S2352-3018(19)30034-7. Epub 2019 Apr 2.
- Prabhu S, Mehta SH, McFall AM, Srikrishnan AK, Vasudevan CK, Lucas GM, Celentano DD, Solomon SS. Substance use is associated with condomless anal intercourse among men who have sex with men in India: a partner-level analysis. BMC Public Health. 2022 Apr 11;22(1):722. doi: 10.1186/s12889-022-13192-y.
- Solomon SS, Quinn TC, Solomon S, McFall AM, Srikrishnan AK, Verma V, Kumar MS, Laeyendecker O, Celentano DD, Iqbal SH, Anand S, Vasudevan CK, Saravanan S, Thomas DL, Sachdeva KS, Lucas GM, Mehta SH. Integrating HCV testing with HIV programs improves hepatitis C outcomes in people who inject drugs: A cluster-randomized trial. J Hepatol. 2020 Jan;72(1):67-74. doi: 10.1016/j.jhep.2019.09.022. Epub 2019 Oct 8.
- Solomon SS, Mehta SH, McFall AM, Srikrishnan AK, Saravanan S, Laeyendecker O, Balakrishnan P, Celentano DD, Solomon S, Lucas GM. Community viral load, antiretroviral therapy coverage, and HIV incidence in India: a cross-sectional, comparative study. Lancet HIV. 2016 Apr;3(4):e183-90. doi: 10.1016/S2352-3018(16)00019-9. Epub 2016 Mar 11.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- NA_00047702
- R01DA032059 (U.S. NIH Grant/Contract)
- R01MH089266 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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