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Fostering Resilience to Psychosocial and HIV Risk in Indian MSM

Primary Purpose

HIV Infection, Sexual Behavior, Health Behavior

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Self-acceptance based intervention
HIV/STI counseling and testing
Sponsored by
Massachusetts General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for HIV Infection focused on measuring HIV risk behavior

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria - One of the following must be true:

  • Participant has had anal sex with 4 or more male partners (protected or unprotected) in the past 4 months.
  • Participant has had condomless anal sex with a man who was HIV unknown or serodiscordant in the past 4 months.
  • Participant has a history of transactional sex activity in the past 4 months.
  • Participant has been given a diagnosis of an STI in the past 4 months.

Exclusion Criteria:

  • Participant does not identify as male
  • Younger than 18
  • Is unable to understand or consent to the procedures
  • Is deemed by the local PI or study staff to be engaging in deception about the inclusion/exclusion criteria.

Sites / Locations

  • Massachusetts General Hospital
  • The National Institute for Research in Tuberculosis
  • The Humsafar Trust

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Self-acceptance behavioral intervention

Comparison/Control

Arm Description

The intervention will consist of individual and 4 group counseling sessions and 6 individual counseling sessions. The individual sessions are focused on specific individualized risk reduction plans, whereas the group sessions are focused on increasing self-acceptance and reducing HIV risk. Additionally, participants in this arm will receive HIV and STI counseling and testing.

The comparison group will receive HIV and STI counseling and testing.

Outcomes

Primary Outcome Measures

Changes in frequency of condomless sex
Self-reported insertive or receptive anal sex without the use of a condom.
Number of incident STIs from Baseline
Chlamydia, gonorrhea, syphilis, and HIV

Secondary Outcome Measures

Changes in Psychosocial Mediators
Items will be used to measure potential psychosocial mediators (e.g. self-acceptance questionnaire, distress questionnaire) at each major visit.
Cost-effectiveness of intervention
To assess the incremental cost-effectiveness of the experimental versus the comparison condition.

Full Information

First Posted
April 23, 2015
Last Updated
October 22, 2019
Sponsor
Massachusetts General Hospital
Collaborators
National Institute of Mental Health (NIMH), The National Institute for Research in Tuberculosis, Indian Council of Medical Research, Sahodaran, The Humsafar Trust, Fenway Community Health
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1. Study Identification

Unique Protocol Identification Number
NCT02556294
Brief Title
Fostering Resilience to Psychosocial and HIV Risk in Indian MSM
Official Title
Fostering Resilience to Psychosocial and HIV Risk in Indian MSM
Study Type
Interventional

2. Study Status

Record Verification Date
October 2019
Overall Recruitment Status
Completed
Study Start Date
June 2015 (Actual)
Primary Completion Date
August 2019 (Actual)
Study Completion Date
August 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Massachusetts General Hospital
Collaborators
National Institute of Mental Health (NIMH), The National Institute for Research in Tuberculosis, Indian Council of Medical Research, Sahodaran, The Humsafar Trust, Fenway Community Health

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
India has the world's third largest HIV epidemic and men who have sex with men (MSM) are an identified high risk group. MSM in India face unique psychosocial stress underlying the context of HIV risk. To maximize the potential impact of an HIV prevention intervention, the purpose of this study is to test, in a two-arm randomized controlled efficacy trial, a behavioral intervention that addresses both psychosocial / contextual stress and reducing participant's risk for HIV.
Detailed Description
India has the world's third largest HIV epidemic, and MSM in India have an estimated seroprevalence of 14.7%. Many HIV prevention efforts for MSM in India are limited to condom distribution and HIV education, with no existing efficacy trials of HIV prevention interventions and therefore no evidenced based HIV prevention interventions this population. MSM in India are hidden, stigmatized, and face considerable psychosocial stressors, including pressure to marry, which potentially increases the risk for HIV transmission to their wives. This proposal is the culmination of our ongoing, successful > 10-year community based research collaboration with two NGOs dedicated to HIV prevention among MSM, Sahodaran (Chennai) and The Humsafar Trust (Mumbai), and investigators from the India Council of Medical Research (ICMR), National Institute for Research in Tuberculosis (NIRT) in Chennai. Our work, including extensive community advisory input, has identified self-acceptance as a key resilience variable that protects against both HIV risk and psychosocial distress. A field test and pilot randomized controlled trial of our behavioral intervention that addresses both HIV risk and self-acceptance showed high participant acceptability and feasibility of study procedures, and success reducing HIV sexual risk behavior. The current study is a two-arm randomized controlled trial to reduce HIV, STI and sexual transmission risk compared to HIV/STI counseling and testing alone.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infection, Sexual Behavior, Health Behavior
Keywords
HIV risk behavior

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
608 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Self-acceptance behavioral intervention
Arm Type
Experimental
Arm Description
The intervention will consist of individual and 4 group counseling sessions and 6 individual counseling sessions. The individual sessions are focused on specific individualized risk reduction plans, whereas the group sessions are focused on increasing self-acceptance and reducing HIV risk. Additionally, participants in this arm will receive HIV and STI counseling and testing.
Arm Title
Comparison/Control
Arm Type
Other
Arm Description
The comparison group will receive HIV and STI counseling and testing.
Intervention Type
Behavioral
Intervention Name(s)
Self-acceptance based intervention
Intervention Description
The intervention will consist of HIV/STI counseling and testing as well as individual counseling sessions and group sessions. The primary focus of the group sessions are to help foster self-acceptance by the support from the group, as well as learn skills to reduce distress and HIV risk. The primary purpose of the individual sessions is to help develop and implement an individualized plan for HIV risk reduction, and, as needed and available, linkage to other services.
Intervention Type
Behavioral
Intervention Name(s)
HIV/STI counseling and testing
Intervention Description
The counseling component is standard of care in India and will focus on HIV/STI risk and how to minimize risk. This is followed by biological testing for HIV and STIs.
Primary Outcome Measure Information:
Title
Changes in frequency of condomless sex
Description
Self-reported insertive or receptive anal sex without the use of a condom.
Time Frame
4 month visit, 8 month visit, 12, month visit
Title
Number of incident STIs from Baseline
Description
Chlamydia, gonorrhea, syphilis, and HIV
Time Frame
12 month visit
Secondary Outcome Measure Information:
Title
Changes in Psychosocial Mediators
Description
Items will be used to measure potential psychosocial mediators (e.g. self-acceptance questionnaire, distress questionnaire) at each major visit.
Time Frame
Measured at baseline, 4, 8, 12 month visits
Title
Cost-effectiveness of intervention
Description
To assess the incremental cost-effectiveness of the experimental versus the comparison condition.
Time Frame
12 months

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria - One of the following must be true: Participant has had anal sex with 4 or more male partners (protected or unprotected) in the past 4 months. Participant has had condomless anal sex with a man who was HIV unknown or serodiscordant in the past 4 months. Participant has a history of transactional sex activity in the past 4 months. Participant has been given a diagnosis of an STI in the past 4 months. Exclusion Criteria: Participant does not identify as male Younger than 18 Is unable to understand or consent to the procedures Is deemed by the local PI or study staff to be engaging in deception about the inclusion/exclusion criteria.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steven A Safren, PhD
Organizational Affiliation
University of Miami
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Matthew J Mimiaga, ScD, MPH
Organizational Affiliation
Brown University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Conall M O'Cleirigh, Ph.D.
Organizational Affiliation
Massachusetts General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Massachusetts General Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States
Facility Name
The National Institute for Research in Tuberculosis
City
Chennai
Country
India
Facility Name
The Humsafar Trust
City
Mumbai
Country
India

12. IPD Sharing Statement

Citations:
PubMed Identifier
33740407
Citation
Safren SA, Thomas B, Biello KB, Mayer KH, Rawat S, Dange A, Bedoya CA, Menon S, Anand V, Balu V, O'Cleirigh C, Klasko-Foster L, Baruah D, Swaminathan S, Mimiaga MJ. Strengthening resilience to reduce HIV risk in Indian MSM: a multicity, randomised, clinical efficacy trial. Lancet Glob Health. 2021 Apr;9(4):e446-e455. doi: 10.1016/S2214-109X(20)30547-7.
Results Reference
derived
PubMed Identifier
30021566
Citation
Mimiaga MJ, Thomas B, Mayer KH, Regenauer KS, Dange A, Andres Bedoya C, Rawat S, Balu V, O'Cleirigh C, Biello KB, Anand V, Swaminathan S, Safren SA. A randomized clinical efficacy trial of a psychosocial intervention to strengthen self-acceptance and reduce HIV risk for MSM in India: study protocol. BMC Public Health. 2018 Jul 18;18(1):890. doi: 10.1186/s12889-018-5838-2.
Results Reference
derived

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Fostering Resilience to Psychosocial and HIV Risk in Indian MSM

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