PrEP Restart for Adolescent Girls and Young Women Using STI Self Testing and Assessment of Risk

HIV Prevention Clinical Trial

— PALESA  

Official title:

A Pilot Randomized Controlled Trial to Assess a Model of Decentralised STI-Self Testing and Risk Self-Assessment Among Adolescent Girls and Young Women in South Africa to Trigger PrEP Re-start

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06030856
• Other study ID #: PALESA
• Status: Recruiting
• Phase: N/A
• Start date: July 5, 2023
• Est. completion date: August 2024

Study information

• Verified date: September 2023
• Source: Wits RHI Research Centre Clinical Research Site
• Contact: Thesla Palanee-Phillips
• Phone: 11 358 5471
• Email: TPalanee[@]wrhi.ac.za
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a pilot randomized trial among 50 AGYW (aged ≥16≤18 years), who discontinued PrEP use within the past 6 months, assigned in a 1:1 ratio to receive: 1) STI self-test kits (Neisseria gonorrhoea (NG), Chlamydia trachomatis (CT) and Trichomonas vaginalis (TV)) with in-person instruction at enrolment and telephone/video-based instructions for home use coupled with self-administered behavioural risk assessment or 2) self-administered behavioural risk assessment only (standard of care). All participants will receive comprehensive sexual and reproductive health (SRH) services during their study visits including choice of family planning method initiation and support, and behavioural HIV/STI risk reduction counselling.

Description:

The PALESA study aims to determine the feasibility of conducting a randomized controlled trial (RCT) to determine the impact of decentralized sexually transmitted infection (STI) point of care (POC) self-testing and risk self-assessment interventions to trigger pre-exposure prophylaxis (PrEP) re-start among adolescent girls and young women (AGYW) in South Africa at potential ongoing risk of re- acquiring STIs and HIV. This overall study comprises two components that include a formative research study enrolling ~60 participants for qualitative in-depth interviews (IDIs) (this has been completed) and a prospective cohort study (Pilot randomized controlled trial - RCT) enrolling 50 AGYW with both clinical, diagnostic laboratory and nested qualitative methodologies. The RCT seeks to establish the feasibility of conducting a randomized controlled trial among AGYW in South Africa to determine the impact of decentralized or at-home STI testing [(for Neisseria gonorrhea (NG), Chlamydia trachomatis (CT) and Trichomonas vaginalis (TV)] on restarting PrEP relative to a self-administered behavioural risk assessment. Additionally qualitative interviews will be conducted to assess adolescent girls experiences of at-home STI testing, behavioural risk assessment, and re-starting PrEP while participating in the pilot trial through exit interviews. Objective 1: To determine the feasibility and acceptability of conducting a RCT among South African AGYW to determine the impact of STI self-testing coupled with a self-administered behavioural risk assessment on restarting PrEP relative to a self-administered behavioural risk assessment only Objective 2: To assess AGYW acceptability of and experiences with use at-home STI testing, self-administered behavioural risk assessment, and re-starting PrEP while participating in the pilot RCT

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 50
• Est. completion date: August 2024
• Est. primary completion date: August 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 16 Years to 20 Years

Eligibility

Inclusion Criteria:

• For the full cohort, all participants must:
• Be cis-gender adolescent females (16-20 years of age)
• Be literate
• Currently sexually active
• Be willing to participate in in-person and virtual study visits
• Not be pregnant or planning to be pregnant for the next 6 months
• Be HIV-negative but not ready to initiate PrEP at the screening and enrolment visit
• Have used PrEP with subsequent discontinuation within the last 6 months
• Have no contraindications to oral PrEP per self-report
• Have no indication of possible acute HIV infection, according to South African PrEP guidelines
• Have their own personal smart phone
• Willing to provide written informed consent/assent to participate in this study

For the subset invited to qualitative interviews, all participants must be:

• Willing to participate in an IDI at/before their month 6 visit (study exit visit)

Exclusion Criteria:

• Potential AGYW participants who meet any of the following criteria will be excluded

from the study:

• At Screening and Enrollment, parent/guardian (for those participants <18 years) is unwilling to provide written informed consent
• At Screening and Enrollment, is already participating in another research study involving drugs, medical devices, or vaccines for STI prevention or treatment.
• Is not willing to comply with study procedures
• As determined by the PIs/designee, any current or historical physical health, mental health or social issue or condition that the site investigator or designee determines should exclude participation.
• Has any other condition that, in the opinion of the PIs/designee, would preclude informed consent, make study participation unsafe, or otherwise interfere with achieving the study objectives.

Related Conditions & MeSH terms

• HIV Prevention

Intervention

Device:
• STI test kits (NG, CT and TV) for home use
The adolescent randomized to the at-home STI testing arm will be provided with in-person instruction at enrollment and flyers (in English and isiZulu) with printed step-by-step instructions for kit use. Information will include details on how to store the kits, criteria for adequate specimen collection and preparation, how to run the test, and how to interpret the test results. Video-based instructions with accompanying text subtitles and audio options may also be provided for home use.

Behavioral:
• Self Administered Behavioural Risk Assessment
Self Administered assessment to determine risk of HIV, STIs and pregnancy

Locations

Country	Name	City	State
South Africa	Wits RHI Research Centre	Hillbrow	Gauteng

Sponsors (3)

Lead Sponsor	Collaborator
Wits RHI Research Centre Clinical Research Site	University of Alabama at Birmingham, University of California, San Francisco

Country where clinical trial is conducted

South Africa, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of participants enrolled and retained in the PALESA study	A recruitment target of 50 adolescent girls and young women and over 90% retention of those participants is achieved	1 year
Primary	Assessing Risk of Acquiring HIV and STIs	A self administered behavioural risk assessment questionnaire with 16 - 20 questions (which include questions on STI test results), which will tally up a score, will be used to measure how much counselling and guidance will the participants need to restart PrEP.; A score of 0 - 7 means medium recommendation to restart PrEP. A score 8-15 means a strong recommendation to restart PrEP. Test results of STIs from the self-testing STI kit are shared on the self-administered behavioural risk assessment questionnaire.	1 year
Primary	Number of participants that restarted PrEP	There will be a dispensation form for every participant, this form will indicate if PrEP was restarted by the participant, and it will calculate include pill counts when PrEP bottles are returned to the research site	1 year
Primary	PrEP continuation 1 month after re-start	Dried Blood Spot (DBS) collected to measure tenofovir diphosphate (TFV-DP) level as an objective assessment of adherence to PrEP.	1 year
Primary	Experiences of at-home STI testing, self-administered behavioural risk assessment, and re-starting PrEP	In-Depth Interviews will be conducted to collect participant's experience while in the study and tools used during the study.	1 year