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PrEP (Pre-exposure Prophylaxis) Stigma and Women Ethnodrama Pre-Test Phase

Designing an Ethnodrama Addressing PrEP Stigma Toward Young Cisgender Women in Kenya

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06501885
Enrollment
63
Registered
2024-07-15
Start date
2024-11-11
Completion date
2025-09-03
Last updated
2026-07-29

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

Conditions

HIV

Keywords

Stigma, HIV, PrEP

Brief summary

The investigators will develop and pre-test an ethnodrama intervention designed to transform community member beliefs about and foster support of young cisgender women (YCW) using PrEP.

Detailed description

In Aim 1/Year 1, the investigators will develop the ethnodrama intervention; no data collection activities are included. In Aim 2/Year 2, the investigators will pre-test the ethnodrama intervention with invited groups of young women and members of young women's socio ecology (i.e., male partners, female peers, healthcare providers, informal community leaders, and family members).

Interventions

The intervention is six drama performances that are designed to transform community member beliefs about and foster support of young women's PrEP use, reduce PrEP-related enacted stigma toward young women, and reduce PrEP-related anticipated and internalized stigma among young women.

Sponsors

Duke University
Lead SponsorOTHER
National Institutes of Health (NIH)
CollaboratorNIH
Fogarty International Center of the National Institute of Health
CollaboratorNIH

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* 18 years of age or older * Young cisgender women who have taken or are taking PrEP * Male partners of young women * Female peers of young women * Healthcare providers * Informal community leaders * Family members of young women

Exclusion criteria

None

Design outcomes

Primary

MeasureTime frameDescription
Acceptability of the intervention storylines and interactive componentsImmediately post-interventionThe investigators will gather feedback on the acceptability of the storylines (e.g., perceptions of whether the storylines seem relatable) and interactive components, as measured by several single-item questions scored from 1 (strongly agree) to 6 (strongly disagree), with lower scores reflecting greater acceptability.

Secondary

MeasureTime frameDescription
Potential effectiveness of the intervention's storylines on "transporting" participants, as measured by a brief interviewer-administered survey using the Narrative Transportation Scale (NTS).Immediately post-interventionThe Storytelling/Narrative Theory (Lee et al., 2016) suggests that when audiences become deeply absorbed in a story (i.e., when the story is relatable and audiences identify with the characters), they are more likely to reflect on and reconsider their existing beliefs, attitudes, and behaviors. The NTS includes 12 items scored from 1 (strongly agree) to 6 (strongly disagree), with lower scores reflecting greater transportation into the story. Example questions include: "While you were watching the play, you could easily see the stories in it taking place in real life." and "You could picture yourself or someone you know in the stories described in the play."

Countries

Kenya

Contacts

PRINCIPAL_INVESTIGATORAmy Corneli, PhD, MPH

Duke University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 30, 2026