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Reducing HIV Stigma for African American Women

Reducing HIV Stigma to Improve Health Outcomes for African-American Women

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01893112
Enrollment
240
Registered
2013-07-08
Start date
2013-06-30
Completion date
2017-02-28
Last updated
2017-05-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV

Brief summary

African American women account for 66% of HIV infections in women in the U.S., AIDS is a leading cause of death for African American women, and African Americans have the lowest medication adherence rates compared to other groups in the U.S. One of the reasons for low medication adherence among African Americans is fear of stigma. HIV stigma has been linked to depression, psychological distress, poor quality of life, poor medication adherence and service utilization contributing to morbidity and mortality. Research has found that stigma is a moderator to poor adherence via depressive symptoms. The current study is a randomized control trial with a time and attention control group to test the effectiveness of a stigma reduction intervention adapted for use with African American women. A total of 224 African American women will be recruited to participate in the study. Half of the women will be from Chicago, Illinois (112) and the other half will be from Birmingham, Alabama (112). A workshop will be held once a study site has recruited 28 women, half of the women will be in the intervention group (14) and the other half will be in the control group (14). Each study site will have 4 cohorts of 28 women. The main aims of the current study are: 1. to determine the long-term effectiveness of the intervention to reduce stigma for African American women living with HIV in Chicago Illinois and Birmingham, Alabama 2. to examine whether stigma reduction due to the intervention is associated with improved physical health biomarkers (CD4+ T cell count, viral load), mediated by reduced psychological symptoms (depressive symptoms), improved engagement to care, and improved medication adherence 3. to explore whether stigma reduction due to the intervention is moderated by location (Chicago vs. Birmingham), transmission risk factor, time since diagnosis, and perceived social support We expect that the multimedia workshop intervention will demonstrate effectiveness in reducing internalized stigma through an easily-disseminated method, and that it will have a positive impact on medication adherence and engagement in care for African American women living with HIV.

Interventions

BEHAVIORALUnity Workshop

The intervention is based on other stigma reduction programs that are being used internationally (HIV Stigma Toolkit developed by the International Center for Research on Women and trigger videos developed by International Training & Education Center for health).

BEHAVIORALBreast Cancer Screening

Sponsors

University of Alabama at Birmingham
CollaboratorOTHER
Northwestern University
CollaboratorOTHER
National Institute of Mental Health (NIMH)
CollaboratorNIH
University of Washington
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* they are women who identify as having an African American racial/ethnic background * born in the U.S. (including women of Caribbean origin if born in the U.S. * speak and understand English as their primary language of communication outside the home * they are 18 years of age or older * have a documented HIV positive status (women are on antiretroviral treatment and women who are not on antiretroviral are eligible) * able to see and interact with a touchscreen computer in English.

Exclusion criteria

* women who not self-identify as African American * women who are African born or born outside the United States * younger than 18 years of age * unable to provide informed consent * life expectancy less than 1 year per physician report * unable to see and interact with a touchscreen computer in English.

Design outcomes

Primary

MeasureTime frameDescription
Change in stigma scores from baseline to 12 months.baseline, after intervervention, 4 months, 6 months, 8 months, 12 monthsWe will see if the intervention/workshop reduces HIV related stigma after 1 year in the study. We will use the Stigma Scale for Chronic Illness to measure stigma.

Secondary

MeasureTime frameDescription
Post-Traumatic Stress Disorder Checklistbaseline, 12 months
Adherence to HIV Medicationbaseline, after intervention, 4 months, 6 months, 8 months, 12 monthsAdherence to HIV medication will be measured by participants self report of adherence using commonly used set of questions.
Patient Health Questionnaire (PHQ-9)baseline, after intervention, 4 months, 6 months, 8 months, 12 monthsWe will look at the correlation between stigma scores and depression scores over time.
Medical Outcomes Study Social Support ScaleStudy durationWe are going to use a validated social support scale, and analyze social support as a correlate.
Location as a moderator variablebaseline, after intervervention, 4 months, 6 months, 8 months, 12 monthsThis is a multi-site study (Chicago and Birmingham) and we are interested in seeing if location is a moderating variable
Engagement in Care (from patient record)baseline, 4 months, 8 months, 12 monthsResearch assistants will access participants' medical records to see if patients have missed any HIV related visits (i.e. medical, counseling). Engagement to care will be measured as a proportion (missed visits over total scheduled). Rescheduled visits will not count as missed visits. At baseline, we will look at visits for the past 12 months.
HIV viral load (from medical chart) over 1 year study durationbaseline, 4 months, 8 months, 12 monthsWe want to examine whether stigma reduction due to the intervention is associated with improved physical health bio-markers such as suppression in HIV viral load in the blood (taken from medical chart/previous clinical blood tests).
Change in CD4 countbaseline, 4 months, 8 months, 12 monthsWe want to see wither stigma reduction from the intervention associated with improved physical health bio-markers such as CD4+ T cell count.
substance abusebaseline, 12 monthssubstance use and stigma of substance use will be measured using: Alcohol Use disorders Identification Test (AUDIT) Severity of Dependence Scale (SDS) Substance Abuse Self Stigma (SASS)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026