Standardized Patients to Measure and Address Intersectional Stigma

  • STATUS
    Recruiting
  • days left to enroll
    12
  • participants needed
    56
  • sponsor
    University of Minnesota
Updated on 3 September 2021
HIV Vaccine
enzyme-linked immunosorbent assay

Summary

This study aims to develop and evaluate an intervention to reduce enacted stigma in healthcare settings aimed at people living with HIV (PLWH) and men who have sex with men (MSM) in China. Enacted stigma will be measured using a quality of care score collected through unannounced standardized patient (SP) visits to consenting providers in sexual health clinics.

Description

Standardized patients, or trained actors from the community, will conduct a baseline round of unannounced clinic visits with consenting providers for the purposes of observing their clinical performance. SPs will present clinically standardized case scenarios, but the HIV status and sexual orientation of each case will be randomly varied in order to quantify the extent to which HIV stigma and/or homophobia contribute to the deterioration of care quality. Care quality will be calculated using a global score based on a standard checklist administered to SPs following each visit. Results of the baseline visit will inform the development of a stigma reduction intervention for consenting providers employed at clinics randomized to the treatment arm of the study. Design of this intervention has been informed by results of the baseline study and incorporates expert input from members of community advisory boards (CAB), one made up of community members and the other of providers. The intervention will consist of both didactic and skills-building methods and will be delivered both in-person and through follow-up modules online. Didactic portions will include content on topics including clinical management of common STIs, shared decision making, sexual history taking, and working with marginalized populations. Skills-building sessions will include group-based discussion and medical simulation and feedback with trained standardized patients. Follow-up data collection will begin within 2 months of completing the stigma reduction intervention using the same approach as for the baseline data collection. All research activities will take place in Guangzhou, China.

Details
Condition HIV, HIV positive, HIV infection, Immunodeficiency, AIDS Vaccines, AIDS, HIV/AIDS, HIV Infections, human immunodeficiency virus, hiv disease, HIV Vaccine, hiv vaccines, acquired immunodeficiency syndrome (aids), sida, acquired immune deficiency syndrome (aids)
Treatment Stigma Reduction Intervention
Clinical Study IdentifierNCT04896216
SponsorUniversity of Minnesota
Last Modified on3 September 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Eligible facilities will be those with
formal government accreditation as a medical center (a basic tenet of all public hospitals in China); and
possession of an accredited on-site laboratory with capacity to provide enzyme-linked immunosorbent assay testing for HIV, treponemal (e.g. Treponema pallidum particle agglutination) and non-treponemal tests (e.g. rapid plasma regain) for syphilis
Within eligible and consenting facilities, eligible providers will be those who are licensed at the time of the study to practice dermatovenereology in China

Exclusion Criteria

none
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