RISE: Reducing Cancer and HIV Stigma Through Empowerment
Starting soon · Not applicable
Conditions studied: HIV, Cervical Cancer Stigma
In brief
This multilevel randomized behavioral study evaluates participant- and provider-level stigma-reduction interventions in Zambia. Participant-level intervention: Women living with cervical cancer and HIV (WLC+H ) are randomized in a 2×2 factorial design of storytelling versus neutral videos and storytelling versus neutral disclosure interventions to assess effects on quality of life, anxiety, and depressive symptoms. Provider-level intervention: Healthcare workers are randomized to storytelling or neutral videos to assess changes in stigma and compassion. The study also evaluates participant -reported stigma and satisfaction with care before and after implementation of the provider intervention.
Key facts
- Study ID
- NCT07728370
- Run by
- M.D. Anderson Cancer Center
- People needed
- 440
- Starts
- 2026-09-01
- Expected to finish
- 2030-08-31
- Last updated by the study team
- 2026-07-27
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patient-level intervention
- Women diagnosed with cervical cancer and HIV (stage I-IV)
- Receiving cancer treatment at the Cancer Disease Hospital in Zambia
- Aged 18 or above 4. Able to speak in English (the official language in Zambia) or one of four local languages (Bemba, Nyanja, Tonga, Lozi) for cultural inclusivity
- Provider-level intervention
- Employment at the Cancer Disease Hospital in Lusaka, Zambia
You may not qualify if…
- Patient-level intervention
- Inability to provide informed consent and presence of a major mental health disorder (e.g., schizophrenia or bipolar disorder), as determined by participant records or self-report.
- Provider-level intervention
- Inability to provide informed consent
Where it is running
- UT MD Anderson — Houston, Texas, United States
Full record on ClinicalTrials.gov
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