search
Back to results

A Pragmatic Trial to Expand Youth-friendly HIV Self-testing (I-TEST)

Primary Purpose

HIV/AIDS, Sexually Transmitted Infections

Status
Active
Phase
Not Applicable
Locations
Nigeria
Study Type
Interventional
Intervention
Sexual health information
I-TEST branded HIVST package
Follow-up testing and clinic assessments
Sponsored by
St. Louis University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for HIV/AIDS focused on measuring HIV Prevention, HIV Self-testing, Young people, Nigeria, 4 Youth by Youth

Eligibility Criteria

14 Years - 24 Years (Child, Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Nigerian Institute of Medical Research

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

I-TEST Intervention Package

Arm Description

Each 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.

Outcomes

Primary Outcome Measures

Uptake of HIV Self-testing
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 to verify the HIVST results. The number of persons who tested with an HIV self-test

Secondary Outcome Measures

Uptake of Facility-Based HIV testing
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) Testing
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).
Sexually Transmitted Infection (STI) Treatment
The number of persons initiating STI treatment among the total number of persons with active infection linked to care.
PrEP Referral
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 Use
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 Engagement
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.
Cost effectiveness of the intervention
The incremental cost-effectiveness ratio of participants involved in the I-TEST intervention phase compared to the control phase.

Full Information

First Posted
December 19, 2020
Last Updated
August 13, 2023
Sponsor
St. Louis University
Collaborators
University of North Carolina, Chapel Hill, Nigerian Institute of Medical Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH)
search

1. Study Identification

Unique Protocol Identification Number
NCT04710784
Brief Title
A Pragmatic Trial to Expand Youth-friendly HIV Self-testing
Acronym
I-TEST
Official Title
The 4 Youth by Youth Project: A Pragmatic Stepped-wedge Cluster Randomized Controlled Trial to Expand Youth-friendly HIV Self-testing Services in Nigeria
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
May 10, 2021 (Actual)
Primary Completion Date
August 2023 (Anticipated)
Study Completion Date
April 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
St. Louis University
Collaborators
University of North Carolina, Chapel Hill, Nigerian Institute of Medical Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV/AIDS, Sexually Transmitted Infections
Keywords
HIV Prevention, HIV Self-testing, Young people, Nigeria, 4 Youth by Youth

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Sequential Assignment
Model Description
Stepped-wedge cluster randomized controlled trial
Masking
None (Open Label)
Allocation
N/A
Enrollment
1500 (Actual)

8. Arms, Groups, and Interventions

Arm Title
I-TEST Intervention Package
Arm Type
Experimental
Arm Description
Each 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.
Intervention Type
Behavioral
Intervention Name(s)
Sexual health information
Other Intervention Name(s)
Pre-Implementation (Control Phase)
Intervention Description
We will provide participants with sexual health information, that is basic, accurate, and directly contributes to health-promoting decisions and behavior, once a week at the beginning of the study.
Intervention Type
Behavioral
Intervention Name(s)
I-TEST branded HIVST package
Other Intervention Name(s)
Intervention Implementation
Intervention Description
The I-TEST branded HIVST package will include HIV self-testing (HIVST) kits, referral coupons, condoms, female or male hygiene products, and instructions on how to use the I-TEST photo verification App or USSD (Unstructured Supplementary Service Data) system to verify the HIVST results. Study participants will be referred to a youth-friendly health clinic for confirmatory HIV testing, STI testing (syphilis, gonorrhea, chlamydia, and hepatitis B), STI treatment and PrEP referral.
Intervention Type
Other
Intervention Name(s)
Follow-up testing and clinic assessments
Other Intervention Name(s)
Post-Implementation
Intervention Description
Information to encourage routine retesting for HIV every 6 months and linkage to the youth-friendly clinic for confirmatory HIV testing, STI testing (syphilis, gonorrhea, chlamydia, and hepatitis B), STI treatment, and PrEP referral. Additionally, follow-up surveys will be administered to assess HIV testing, sexual behavior history, youth participation experience, and other related outcomes will be collected from enrolled participants.
Primary Outcome Measure Information:
Title
Uptake of HIV Self-testing
Description
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 to verify the HIVST results. The number of persons who tested with an HIV self-test
Time Frame
Up to 24 months
Secondary Outcome Measure Information:
Title
Uptake of Facility-Based HIV testing
Description
The number of persons who received an HIV test at a youth-friendly clinic among the total number of participants in the study.
Time Frame
Up to 24 months
Title
Sexually Transmitted Infection (STI) Testing
Description
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).
Time Frame
Up to 24 months
Title
Sexually Transmitted Infection (STI) Treatment
Description
The number of persons initiating STI treatment among the total number of persons with active infection linked to care.
Time Frame
Up to 24 months
Title
PrEP Referral
Description
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.
Time Frame
Up to 24 months
Title
100% Condom Use
Description
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.
Time Frame
Up to 24 months
Title
Youth Engagement
Description
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.
Time Frame
Up to 24 months
Title
Cost effectiveness of the intervention
Description
The incremental cost-effectiveness ratio of participants involved in the I-TEST intervention phase compared to the control phase.
Time Frame
Up to 24 months
Other Pre-specified Outcome Measures:
Title
Key Implementation Factors
Description
Guided by the RE-AIM framework for implementation science, semi-structured, in-depth interviews will be conducted at the individual and setting level to explore the factors associated with the implementation of the intervention (e.g., reach, adoption, implementation, and maintenance).
Time Frame
Up to 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
24 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Juliet Iwelunmor, PhD
Organizational Affiliation
St. Louis University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Oliver Ezechi, MD
Organizational Affiliation
Nigerian Institute of Medical Research
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Joseph Tucker, MD
Organizational Affiliation
University of North Carolina, Chapel Hill
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nigerian Institute of Medical Research
City
Yaba
State/Province
Lagos
ZIP/Postal Code
00000
Country
Nigeria

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Deidentified individual data that supports the results will be shared beginning 9 to 36 months following publication provided the investigator who proposes to use the data has approval from an Institutional Review Board (IRB), Independent Ethics Committee (IEC), or Research Ethics Board (REB), as applicable, and executes a data use/sharing agreement with Saint Louis University.
Citations:
Citation
WHO/TDR. (2018). Crowdsourcing in Health and Health Research: A Practical Guide (TDR/STRA/18.4). Retrieved from Geneva: https://www.who.int/tdr/publications/year/2018/crowdsourcing-practical-guide/en/
Results Reference
background
PubMed Identifier
32469971
Citation
Iwelunmor J, Ezechi O, Obiezu-Umeh C, Gbaja-Biamila T, Nwaozuru U, Oladele D, Musa AZ, Idigbe I, Uzoaru F, Airhihenbuwa C, Muessig K, Conserve DF, Kapogiannis B, Tucker JD. The 4 youth by youth HIV self-testing crowdsourcing contest: A qualitative evaluation. PLoS One. 2020 May 29;15(5):e0233698. doi: 10.1371/journal.pone.0233698. eCollection 2020.
Results Reference
background
PubMed Identifier
33413246
Citation
Obiezu-Umeh C, Gbajabiamila T, Ezechi O, Nwaozuru U, Ong JJ, Idigbe I, Oladele D, Musa AZ, Uzoaru F, Airhihenbuwa C, Tucker JD, Iwelunmor J. Young people's preferences for HIV self-testing services in Nigeria: a qualitative analysis. BMC Public Health. 2021 Jan 7;21(1):67. doi: 10.1186/s12889-020-10072-1.
Results Reference
background
PubMed Identifier
31881959
Citation
Nwaozuru U, Iwelunmor J, Ong JJ, Salah S, Obiezu-Umeh C, Ezechi O, Tucker JD. Preferences for HIV testing services among young people in Nigeria. BMC Health Serv Res. 2019 Dec 27;19(1):1003. doi: 10.1186/s12913-019-4847-x.
Results Reference
background
PubMed Identifier
34800699
Citation
Iwelunmor J, Tucker JD, Obiezu-Umeh C, Gbaja-Biamila T, Oladele D, Nwaozuru U, Musa AZ, Airhihenbuwa CO, Muessig K, Rosenberg N, BeLue R, Xian H, Conserve DF, Ong JJ, Zhang L, Curley J, Nkengasong S, Mason S, Tang W, Bayus B, Ogedegbe G, Ezechi O. The 4 Youth by Youth (4YBY) pragmatic trial to enhance HIV self-testing uptake and sustainability: Study protocol in Nigeria. Contemp Clin Trials. 2022 Mar;114:106628. doi: 10.1016/j.cct.2021.106628. Epub 2021 Nov 17.
Results Reference
derived
Links:
URL
https://4yby.org/
Description
4 Youth by Youth Website
URL
https://www.seshglobal.org/
Description
SESH Crowdsourcing Clinic

Learn more about this trial

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

We'll reach out to this number within 24 hrs