Status:
COMPLETED
Multi-component HIV Intervention Packages for Chinese Men Who Have Sex With Men -Test, Link and Care (TLC)
Lead Sponsor:
Vanderbilt University Medical Center
Collaborating Sponsors:
National Center for AIDS/STD Control and Prevention, China CDC
Conditions:
HIV/AIDS
Eligibility:
MALE
18+ years
Brief Summary
1. The number of MSM who are tested for HIV in the 4 study clinics over 12 months will increase compared with historical data from the same 4 clinics over the past 12 months prior to the intervention....
Eligibility Criteria
Inclusion
- • Men who had sex with another man in the last 12 months based on self-reporting (sex can be defined as oral, anal, or mutual masturbation)(including transgendered women)（including transgendered women）;
- Aged 18 years or older;
- Living and/or working in the defined districts of municipal Beijing;
- Able and willing to adequately grant informed consent. For the purposes of this activity participants must consent to questionnaire surveys, receipt of phone messages, and serological testing;
- Having not previously participated in HIV testing in this study.
- Besides these criteria, additional criteria for the HIV Linkage and Care pilot Research Clinical Trial are:
- Men who are being identified as HIV positive during the testing campaign in Phase I of the study;
- No plan to leave Beijing in the next 12 months.
- Willing to comply with study procedures.
- Having a cell phone and willing to receive study related SMS texts
Exclusion
- Having previously been found to be HIV positive based on self-reporting during eligibility screening;
- Serious psychological disturbance or cognitive impairment interfering with the participant's ability to comply with the study visit schedule and procedures, as judged by the local study clinician;
- Any other medical or psychiatric condition that, in the opinion of the investigator, would make participation in the study unsafe, or otherwise interfere substantially with the study objectives or interpretation.
Key Trial Info
Start Date :
March 1 2013
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
June 1 2016
Estimated Enrollment :
3760 Patients enrolled
Trial Details
Trial ID
NCT01904877
Start Date
March 1 2013
End Date
June 1 2016
Last Update
April 5 2017
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