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Community Popular Opinion Leader Intervention for HIV Prevention Uptake in Rural South Africa

Adapting and Piloting a Community Popular Opinion Leader Intervention to Increase Uptake of HIV Prevention Interventions in Rural South Africa

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07741474
Acronym
Izinkanyezi
Enrollment
60
Registered
2026-08-03
Start date
2026-08-01
Completion date
2026-10-01
Last updated
2026-08-03

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

Conditions

HIV, Sexually Transmitted Infections (STI)

Keywords

pilot, HIV prevention, behavior change, risk communication, HIV self-testing, social networks

Brief summary

The Community Popular Opinion Leader (CPOL) is an intervention dveloped in the United States which identifies, trains, and enlists key opinion leaders within communities to deliver messages to peers and help link them to services. This project involves testing the feasibility and acceptability of such a localized version of the CPOL intervention in rural South Africa. This will be achieved through a pilot intervention in three purposively selected communities in the Hlabisa sub-district of uMkhanyakude district, KwaZulu-Natal. The investigators will select potential peer leaders in three ways (at random; based on nominations by peers; based on statistical analysis of previously collected social network data). Peer leaders will be invited to attend four weekly training sessions to learn about HIV prevention and persuasive communication. They will then be coached to start HIV prevention conversations with peers, including provision of HIV self-test kits and linkage to healthcare services. The investigators will evaluate this pilot using group discussions, in-depth interviews and brief pre/post questionnaires with session facilitators, peer leaders, contacted peers and healthcare providers. The investigators will analyse the data collected with the Practical, Robust Implementation and Sustainability Model (PRISM) dissemination and implementation framework, identifying factors likely to affect Reach, Effectiveness, Adoption, Implementation and Maintenance (RE-AIM).

Detailed description

The CPOL intervention is a local adaptation of an intervention package developed with Black men-who-have-sex-with-men (MSM) in the United States. This pilot trial studies both the overall effectiveness of this adapated intervention in rural South Africa, and the differential benefit of selecting participants using three different methods: 1) at random; 2) based on peer nominations of local opinion leaders; 3) based on a community-wide social network built from nominations of important social contacts. While the primary outcome is quantitative, the study is not powered to see statistically significant differences between arms. The evaluation focus of the pilot trial is the process evaluation, which will follow the RE-AIM framework to assess how and why the intervention worked, failed or needed adjustment. The end result will be a CPOL-style intervention package that may (or may not) be appropriate for rural South Africa, and a methodology for adapting CPOL packages for other sexual health contexts. The process evaluation will include qualitative group and in-depth one-to-one interviews with: (i) session trainers; (ii) POL trainees; (iii) peers in the local community; (iii) HIV service providers. It will also include a short pre/post questionnaire for all trainees to capture key knowledge and attitude outcomes relating to the training.

Interventions

BEHAVIORALCPOL group training

Trained research assistants will deliver four two-hour training sessions to a group of \~20 young adults, leading to the trainees providing sexual health information and HIV self-tests (with onward self-referral to local clinics) to their friends and close contacts. Sessions include training on local sexual health information, effective communication strategies, practice conversations and feedback.

Sponsors

Africa Health Research Institute
Lead SponsorOTHER
University College, London
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Selection from the population to participate in the intervention is conducted using different methods in each study arm, each defined by a geographic location. Methods are applied to locations at random.

Eligibility

Sex/Gender
ALL
Age
18 Years to 28 Years
Healthy volunteers
Yes

Inclusion criteria

* Resident in Sixhumene study area household

Exclusion criteria

* Unable to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
Number of HIV self-tests distributedFrom enrollment to 4 weeks after last training sessionThe mean number of HIV self-tests distributed to peers by trainees

Secondary

MeasureTime frameDescription
Number of peer conversations heldEnrollemnt to 4 weeks after last training sessionMean number of conversations trainees report holding with peers
Trainee HIV ART knowledge improvementEnrollment to end of last session (4 week period)Mean change in scores pre/post intervention on a 5-item ART knowledge question set \[range 0-5; higher = better\]
Trainee HIV PrEP knowledge improvementEnrollment to end of last session (4 week period)Mean change in scores pre/post intervention on a 5-item PrEP knowledge question set \[range 0-5; higher = better\]
Trainee generalized self-efficacy improvementEnrollment to end of last session (4 week period)Mean change in scores pre/post intervention on the Generalized Self Efficacy-short form (GSE 6) scale \[range 6-24; higher = better\]
Trainee ART/PrEP self-efficacy improvementEnrollment to end of last session (4 week period)Mean change in scores pre/post intervention on a 4-item self-efficacy-short form scale specific to ART and PrEP use \[range 4-16; higher = better\]
Trainee ART/PrEP stigma reductionEnrollment to end of last session (4 week period)Mean change in scores pre/post intervention on a 6-item ART/PrEP use stigma question set \[range 6-24; higher = worse\]

Countries

South Africa

Contacts

CONTACTGuy Harling, ScD
guy.harling@ahri.org+27352510650

Outcome results

None listed

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