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A Pragmatic Trial to Expand Youth-friendly HIV Self-testing

Not Applicable
Completed
Conditions
HIV/AIDS
Sexually Transmitted Infections
Interventions
Behavioral: Sexual health information
Behavioral: I-TEST branded HIVST package
Other: Follow-up testing and clinic assessments
Registration Number
NCT04710784
Lead Sponsor
Washington University School of Medicine
Brief Summary

The current study extends the study team's earlier efforts described in ClinicalTrail ID#: NCT04070287 and NCT03874663. The I-TEST (Innovative Tools to Expand Youth-friendly HIV Self-Testing) study known locally as the 4 Youth by Youth project, sought to develop and evaluate novel youth-friendly HIVST services in Nigeria using open challenges and apprenticeship training informed by a participatory learning collaborative model. The study thus aims to reach young Nigerians that remain undiagnosed for HIV and to facilitate linkage and retention in preventive services (includes STI testing/treatment, PrEP referral, condom use).

Detailed Description

Following the completion of the open contests and apprenticeship training, four youth teams (with four distinct interventions) were selected to undergo a one-year pilot assessment in the community. Preliminary findings from the feasibility study suggest that the youth-developed interventions have the potential to impact HIV testing as well as uptake of sexually transmitted infections (STI) testing among young people in Nigeria. As a result, the investigators identified key components from the four interventions to form a single intervention that will be evaluated in the next phase of the research. Thus, the current protocol is focused on evaluating the effectiveness of a combined, youth-developed intervention on HIV testing and other HIV prevention outcomes (i.e. condom use, PrEP referral, STI testing).

Using a stepped-wedge cluster randomized controlled trial design, the I-TEST intervention package will be implemented sequentially across 32 local government areas (LGA) whereby each LGA will be exposed to a pre-intervention (control), intervention (implementing the intervention), and post-intervention condition, according to a randomized schedule. Young people between the ages of 14-24 years will be recruited from the selected 32 local government areas through in-person events, social media platforms, and online advertisements, clinics, and community centers that cater to young people. We included two additional LGAs in November 2021 to account for civil unrest activities that are taking place across two other study sites. Due to the civil unrest, the implementation of the intervention has been affected hence the addition of the two new sites. Upon enrollment, the study team will collect baseline data on HIV testing history, sexual behavior history, youth participation experience, and other related outcomes from the study participants. Two trained youth alongside one trained supervisor will implement the I-TEST intervention at the LGAs.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
1500
Inclusion Criteria
  • Age 14-24
  • Self-reported HIV negative or unknown HIV status
  • Currently and planning on residing in one of the 30 areas during the next 12 months
  • Able to complete the survey in English (the national language of Nigeria)
  • All participants must agree to informed consent and provide their cell mobile number for follow-up and retention
Exclusion Criteria
  • Younger than 14 and older than 24
  • Inability to comply with the study protocol
  • Illness, cognitive impairment, or threatening behavior with acute risk to self or others
  • No informed consent
  • No contact phone number

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
I-TEST Intervention PackageI-TEST branded HIVST packageEach study site will begin in the baseline, pre-implementation phase, and then be randomized to implement the I-TEST intervention package for a duration of three months, followed by the post-implementation phase.
I-TEST Intervention PackageSexual health informationEach study site will begin in the baseline, pre-implementation phase, and then be randomized to implement the I-TEST intervention package for a duration of three months, followed by the post-implementation phase.
I-TEST Intervention PackageFollow-up testing and clinic assessmentsEach study site will begin in the baseline, pre-implementation phase, and then be randomized to implement the I-TEST intervention package for a duration of three months, followed by the post-implementation phase.
Primary Outcome Measures
NameTimeMethod
Uptake of HIV Self-testingUp to 24 months

The number of persons who tested with an HIV self-test. We will assess the number of persons who tested with an HIV self-test among the total number of participants in the study. The primary outcome will be ascertained using a photographic verification approach via a mobile application or a USSD (Unstructured Supplementary Service Data) system. We will also use self-reported data on HIVST results for those unable to use both systems accurately.

Secondary Outcome Measures
NameTimeMethod
Uptake of Facility-Based HIV testingUp to 24 months

The number of persons who received an HIV test at a youth-friendly clinic among the total number of participants in the study.

Sexually Transmitted Infection (STI) TestingUp to 24 months

The number of persons who completed a consultation at the youth-friendly clinic for STI testing. In addition, the baseline and follow-up surveys include items on knowledge and testing of sexually transmitted infections (gonorrhea, chlamydia, syphilis, and hepatitis B virus).

PrEP ReferralUp to 24 months

PrEP referral will be assessed based on the proportion of participants who are "optimal" (assessed based on the sexual behavioral history and willingness to use PrEP) candidates for PrEP referral and the total number of participants referred for PrEP initiation at the health care facilities.

100% Condom UseUp to 24 months

The baseline and follow-up survey includes items on condom usage in the last sexual intercourse and a 4-item Condom Use Self Efficacy Scale.

Youth EngagementUp to 24 months

A 12-item scale on youth engagement will be used to assess the HIV prevention services proposed by the youth teams. The scale was adapted from the 20-item Tiffany-Eckenrode Program Participation Scale (TEPPS). Responses to the participation items were measured on a 5-point Likert-type scale, ranging from "strongly disagree (0)" to "Strongly agree (4)". Higher TEPPS scores indicate higher levels of program participation. The item is only included in the follow-up survey.

Sexually Transmitted Infection (STI) TreatmentUp to 24 months

The number of persons initiating STI treatment among the total number of persons with active infection linked to care.

Cost effectiveness of the interventionUp to 24 months

The incremental cost-effectiveness ratio of participants involved in the I-TEST intervention phase compared to the control phase.

Trial Locations

Locations (1)

Nigerian Institute of Medical Research

🇳🇬

Yaba, Lagos, Nigeria

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