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Clinical Trials/NCT03320239
NCT03320239
Unknown
Not Applicable

Using HIV Risk Assessment Tool to Promote HIV Testing Among Men Who Have Sex With Men in Beijing: a Social Media-based Randomized Trial

National Center for AIDS/STD Control and Prevention, China CDC1 site in 1 country4,500 target enrollmentOctober 12, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
HIV/AIDS
Sponsor
National Center for AIDS/STD Control and Prevention, China CDC
Enrollment
4500
Locations
1
Primary Endpoint
The proportion of HIV testing during the study period
Last Updated
8 years ago

Overview

Brief Summary

The objective of the study is to evaluate the effectiveness of a HIV risk assessment tool to promote HIV testing and to reduce high risk sexual behaviors among men who have sex with men (MSM). It hypothesizes that the social media-based HIV risk assessment tool can increase 20% HIV testing proportion during the six months follow-up period.

Registry
clinicaltrials.gov
Start Date
October 12, 2017
End Date
May 2018
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Sponsor
National Center for AIDS/STD Control and Prevention, China CDC
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Male at birth.
  • Having had homo-sexual behaviors (anal/oral) in the past 6 months before enrollment.
  • An age of 18 years or older.
  • Living in Beijing, China.
  • Self-reporting HIV negative or unknown.
  • Willingly participating into the baseline survey and the six months follow ups.
  • Agreeing not to share the research link to others.
  • Owning a mobile phone and having had downloaded the social networking Application Blued before enrollment.

Exclusion Criteria

  • Not accepting blood sampling within the study period.
  • Reporting injecting drugs use in the past six months before enrollment.
  • Being currently involved in other HIV behavioral interventions for MSM.
  • Having a specific plan to leave from Beijing in the next 6 months.
  • Self-reporting female.
  • Other reasons the investigators deem make participation either detrimental to the participants or the study.

Outcomes

Primary Outcomes

The proportion of HIV testing during the study period

Time Frame: 1 month

The numerator is the number of participants who come to the specific HIV testing clinics for HIV test during the study period, the denominator is the number of participants randomized per group.

Secondary Outcomes

  • unprotected anal intercourse(6 months)
  • Post exposure prophylaxis (PEP)(6 months)

Study Sites (1)

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