NCT01177995

Brief Summary

This study is a randomized outcome trial of a social network HIV prevention intervention for at-risk labor migrants who have arrived in St. Petersburg, Russia, to seek work. Most come to St. Petersburg from Moldova, Tajikistan, Uzbekistan, Ukraine, and other poor post-Soviet republics. While living in Russia, labor migrants are also living in a city and country with high HIV prevalence. Many labor migrants have limited awareness of AIDS, and most are living in a location far from their spouses, family members, and others. For that reason, labor migrants are vulnerable to risk behavior for contracting HIV. This study hypothesizes that members of labor migrant social networks whose network leaders are trained to deliver HIV prevention messages will exhibit greater reductions in sexual risk behavior (unprotected intercourse with nonspousal partners) from baseline to 3- and 12-month followup assessments than will members of social networks whose members receive standard, individual HIV risk reduction counseling alone.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
207

participants targeted

Target at P75+ for phase_2 hiv

Timeline
Completed

Started Oct 2008

Longer than P75 for phase_2 hiv

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2008

Completed
1.8 years until next milestone

First Submitted

Initial submission to the registry

August 6, 2010

Completed
3 days until next milestone

First Posted

Study publicly available on registry

August 9, 2010

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2011

Completed
1.9 years until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2013

Completed
Last Updated

August 23, 2013

Status Verified

August 1, 2013

Enrollment Period

2.9 years

First QC Date

August 6, 2010

Last Update Submit

August 21, 2013

Conditions

Outcome Measures

Primary Outcomes (1)

  • Unprotected sexual intercourse events with a nonspousal partner

    up to 12 months post intervention

Secondary Outcomes (2)

  • AIDS-related knowledge, attitudes, intentions, perceived norms, and self-efficacy

    up to 12 months post intervention

  • Substance use related to sexual behavior

    up to 12 months post intervention

Study Arms (1)

Social Network

EXPERIMENTAL

Leaders of labor migrant social networks will be trained to disseminate HIV prevention messages to the members of their social networks. The training will sequentially target ways to increase network members' HIV-related knowledge and norms, attitudes, intentions, and confidence in how to avoid risk. Leaders will be encouraged to have these discussions with network members between and after training sessions.

Behavioral: Social Network Intervention

Interventions

Social network leaders will communicate HIV prevention messages to members of their social networks.

Social Network

Eligibility Criteria

Age16 Years+
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • being a labor migrant intending to temporarily work and reside in St. Petersburg, Russia, or being named as a member of the social network of a labor migrant;
  • being at least 16 years old (the age at which persons can be legal labor migrants and are also legally considered to be able to provide informed consent);
  • being able to complete written consent forms and questionnaire measures in Russian, Moldovan, Tajik, or Uzbek language
  • providing written informed consent

You may not qualify if:

  • being younger than age 16;
  • not being able to complete written materials in the Russian, Moldovan, Tajik, or Uzbek language;
  • planning to reside in St. Petersburg, Russia, for less than four months;
  • having a severe mental or developmental disorder apparent by mental status during the study or consent explanation that, in the opinion of a trained interviewer, would preclude ability to understand informed consent or complete study measures

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Officials

  • Yuri A. Amirkhanian, PhD

    Medical College of Wisconsin

    PRINCIPAL INVESTIGATOR
  • Jeffrey A. Kelly, PhD

    Medical College of Wisconsin

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
phase 2
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor of Psychiatry and Behavioral Medicine

Study Record Dates

First Submitted

August 6, 2010

First Posted

August 9, 2010

Study Start

October 1, 2008

Primary Completion

September 1, 2011

Study Completion

August 1, 2013

Last Updated

August 23, 2013

Record last verified: 2013-08