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Increasing MSM in the Continuum of Care in Kazakhstan

Increasing Involvement of MSM in the Continuum of Care in Kazakhstan

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02786615
Enrollment
987
Registered
2016-06-01
Start date
2018-06-27
Completion date
2022-04-30
Last updated
2022-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV, Substance-Related Disorders

Keywords

men who have sex with men (MSM)

Brief summary

This study addresses the disproportionate representation of men who have sex with men (MSM) in the human immunodeficiency virus/acquired immune deficiency syndrome (HIV/AIDS) pandemic in Kazakhstan, a country that has seen some of the largest growth in new HIV infections since the turn of the century. Using a stepped wedge trial across 3 cities in Kazakhstan, the proposed study will test a strategic and innovative social network-based intervention for MSM who use drugs in Kazakhstan as a strategy to increase their numbers in the HIV continuum of care.

Detailed description

The intervention is designed to utilize MSM as experts and leverage social network processes to increase the number of MSM in Kazakhstan to be engaged in the HIV continuum of care. The unit of randomization will be a city, with the timing of roll-out of the social network-based intervention in each of the study's cities-Almaty, Nur-Sultan (formerly Astana), and Shymkent-under experimental control. Receipt/delivery of an intervention to enrolled participants will depend on whether the city is in the intervention delivery phase or not. If a participant is in a city during a time period where the intervention is not being delivered then for that time period, the participant is in the control condition. If the participant is in a city during a time period where the intervention is being delivered then the participant (in fact, all participants in that city) will be considered assigned to the intervention group at that time. In theory, all participants will have the opportunity to experience and receive the intervention. Some participants will be enrolled after the intervention has been rolled out in the city in which they reside; thus, they will only experience the intervention condition and not the control condition.

Interventions

BEHAVIORALPeer Unity

A 4-session, group-delivered intervention focusing on peer/social network-based recruitment and referral program to receive HIV prevention and treatment services in the community.

Sponsors

National Institute on Drug Abuse (NIDA)
CollaboratorNIH
Columbia University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

Stepped-wedge design

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* be at least 18 years old; * identify as male; and * report oral or anal intercourse with another man in the past 12 months; and * report binge alcohol consumption and/or illicit use of substances in the past 12 months

Exclusion criteria

* has a language or cognitive impairment that would prevent comprehension of study procedures, risks, and benefits (described in Russian during the informed consent process)

Design outcomes

Primary

MeasureTime frameDescription
Engagement in the HIV care continuum: HIV testingPast 6 monthsHas participant received an HIV test in the past 6 months

Secondary

MeasureTime frameDescription
For PLWH, engagement in the HIV care continuum related to HIV medical treatmentSince confirmed HIV infection diagnosisFor PLWH, visiting AIDS center, receiving ART, and/or achieving viral suppression (descriptive/exploratory due to limited statistical power given only a smaller fraction of sample will have known HIV infection)

Countries

Kazakhstan, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 2, 2026