NCT01052415

Brief Summary

In this project, UCLA's Center for Community Health (CCH) will develop an efficacious intervention trial integrating both individual and structural components to reduce HIV- related stigma among service providers in China and therefore benefit people living with HIV/AIDS (PLWHA). The purpose of this study is to develop a feasible, practical and low cost intervention strategy that will prevent and/or reduce the negative effects of HIV-related stigma among health service providers in China. This project will be conducted in two provinces and proceed in two phases. In Phase 1, confidential focus groups will take place with small samples of service providers and hospital administrators to finalize the intervention activities, and the investigators will also test and finalize the Audio Computer-Assisted Self-Interview (ACASI) assessment measures and implementation procedures with the same group of service providers. During Phase 1 a small sample of patients will anonymously test the paper-pencil baseline survey. Equal number of samples will be selected from two counties of each province. The findings from Phase 1 will be used to develop intervention, and revise assessment for Phase 2.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
5,400

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Sep 2007

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

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

September 1, 2007

Completed
2.4 years until next milestone

First Submitted

Initial submission to the registry

January 19, 2010

Completed
1 day until next milestone

First Posted

Study publicly available on registry

January 20, 2010

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2010

Completed
8 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2011

Completed
Last Updated

March 18, 2024

Status Verified

March 1, 2024

Enrollment Period

3.3 years

First QC Date

January 19, 2010

Last Update Submit

March 15, 2024

Conditions

Keywords

HIVStigmaPOLService providersChinaUniversal precaution

Outcome Measures

Primary Outcomes (2)

  • HIV related stigma

    6-month and 12-month follow-up

  • Patient satisfaction

    6-mont and 12-month follow-up

Secondary Outcomes (1)

  • Universal precaution

    6-month and 12-month follow-up

Study Arms (2)

Standard care

NO INTERVENTION

Service providers and HIV patients, offered intervention at the end of study

Intervention

EXPERIMENTAL

Behavioral: Cognitive-behavioral, small group format sessions delivered in Chinese to service providers and HIV patients.

Behavioral: Cognitive behavioral sessions

Interventions

Behavioral: Cognitive-behavioral, small group format sessions delivered in Chinese to service providers and HIV patients.

Also known as: Intervention, service providers, HIV-related stigma
Intervention

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Service providers: 18 years and older, who work at the county hospital that is participating in the study, including doctors, nurses and lab technicians, and who provide informed consent.
  • Hospital administrators: 18 years and older, who work at the county hospital that is participating in the study as administrators, and who provide informed consent.
  • Patients: Age 18 and older, who receive treatment from STD, obstetrics/gynecology or HIV care department at the participating hospital, and who provide informed consent.

You may not qualify if:

  • Those who cannot give informed consent (e.g., intoxicated)
  • Those who have a permanent disability (e.g., deaf, serious mental illness, mental retardation).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

UCLA Semel Institute-Center for Community Health

Los Angeles, California, 90024, United States

Location

Related Publications (2)

  • Li L, Liang LJ, Wu Z, Lin C, Guan J. Assessing outcomes of a stigma-reduction intervention with venue-based analysis. Soc Psychiatry Psychiatr Epidemiol. 2014 Jun;49(6):991-9. doi: 10.1007/s00127-013-0808-6. Epub 2013 Dec 28.

  • Li L, Wu Z, Liang LJ, Lin C, Guan J, Jia M, Rou K, Yan Z. Reducing HIV-related stigma in health care settings: a randomized controlled trial in China. Am J Public Health. 2013 Feb;103(2):286-92. doi: 10.2105/AJPH.2012.300854. Epub 2012 Dec 13.

MeSH Terms

Conditions

Patient SatisfactionSocial Stigma

Interventions

Methods

Condition Hierarchy (Ancestors)

Treatment Adherence and ComplianceHealth BehaviorBehaviorSocial Behavior

Intervention Hierarchy (Ancestors)

Investigative Techniques

Study Officials

  • Li Li, PhD

    UCLA Semel Institute, Center for Community Health

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
CARE PROVIDER
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 19, 2010

First Posted

January 20, 2010

Study Start

September 1, 2007

Primary Completion

December 1, 2010

Study Completion

August 1, 2011

Last Updated

March 18, 2024

Record last verified: 2024-03

Locations