MedPath

Initiative for Chinese Sex Workers to Promote Wellbeing and Improve HIV Prevention by Reducing intersEctional Stigma

Not Applicable
Not yet recruiting
Conditions
HIV Prevention
Wellbeing
Registration Number
NCT07103525
Lead Sponsor
NYU Langone Health
Brief Summary

During the development phase (Aim 1), investigators will use a community-driven process to further refine a preliminary intervention design that was developed based on previous research.

For the intervention phase (Aim 2), investigators will conduct a pilot randomized controlled trial of the multi-level intervention. For the individual-level component of the intervention, investigators will recruit 70 Chinese immigrant FSWs who work in MPs in Queens, NYC (n=35 intervention participants and n=35 control participants).

To assess the feasibility and acceptability of intervention implementation (Aim 3), investigators will conduct in-depth qualitative interviews with 12 FSW study participants and the 2 peer advocates and focus groups with 4-5 staff from each of the 3 organizations (3 focus groups total and 12-15 focus group participants in total).

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
Female
Target Recruitment
70
Inclusion Criteria
  • Female Sex Workers: A person who identifies as a woman, Chinese, a massage parlor (MP) worker in Queens, who is at least 18 years old, and has provided sexual services in the past 12 months, will be eligible.
  • Community advisory board (CAB) members: self identifies as a community member providing services to immigrant Chinese women and is at least 18 years old.
  • Peer Advocates: self identifies as current or previous sex worker, is a Chinese adult woman, and speaks both Mandarin and English.
  • Medical Providers: self identifies as a current medical provider who works with Chinese immigrant adults and speaks English.
Exclusion Criteria
  • Female Sex Workers: Because completion of HIV testing is our primary study outcome, women who received an HIV test in the previous 3 months or who know they are HIV-positive will be excluded from the study.
  • Community advisory board (CAB) members: Does not speak English or is under the age of 18.
  • Peer Advocates: Does not speak English/Mandarin or is under the age of 18.
  • Medical Providers: Does not speak English or does not provide care to Chinese immigrant adults (e.g., pediatricians).

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Percentage of Participants who Completed HIV TestingFollow-Up Visit 1 (Approximately Week 6)

Assessed via self-report.

Secondary Outcome Measures
NameTimeMethod
Percentage of Participants with PrEP UptakeFollow-Up Visit 1 (Approximately Week 6)

Assessed via self-report; percentage of participants who begin PrEP treatment.

Trial Locations

Locations (3)

NYU Langone Health

🇺🇸

New York, New York, United States

Columbia University Irving Medical Center

🇺🇸

New York, New York, United States

CUNY-Hunter College

🇺🇸

New York, New York, United States

NYU Langone Health
🇺🇸New York, New York, United States
Sahnah Lim, PhD
Principal Investigator

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