SAPLAI : Assessing the faiSAbility of a Peer-to-peer Contraceptive Education Program on Social Ne… (NCT06943209) | Clinical Trial Compass
CompletedNot Applicable
SAPLAI : Assessing the faiSAbility of a Peer-to-peer Contraceptive Education Program on Social Networks Aimed at 15- to 19-year-old High School Students in GuAdeloupe and La RéunIon
The goal of this clinical trial is to evaluate the feasibility of a contraception education program delivered by peers via social networks to high school students.
Our primary hypothesis is that the implementation of a peer-led contraceptive education program via social networks is a feasible approach in high schools on Reunion Island and Guadeloupe, as part of a before-and-after study.
Our secondary hypotheses concern the evaluation of adoption, exploratory efficacy (on knowledge, attitudes and practices), acceptability and fidelity of the peer-led education program via social networks among high school students in La Réunion and Guadeloupe.
Participants will :
* Participate in a focus group to explore their views and experiences regarding the value of a peer educator as a source of sexual and reproductive health information.
* answer questionnaires on their knowledge of sexual health
* A selected group (peer influencers): Create educational content (after a training period) on sexual health, and particularly contraception, to be broadcast on social networks.
* Take note of the program distributed on the networks by the peer influencers (for 3 months)
* Fill in questionnaires on their knowledge of sexual health, after the program.
Who can participate
Age range
15 Years – 19 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* HIGH SCHOOL STUDENTS
* Young men and women aged between 15 and 19
* Living in La Réunion or Guadeloupe
* Enrolled in one of the selected vocational high schools and whose school principal agrees to take part in the program
* Who have agreed to take part in the study
* Who have received written consent from a parent or guardian.
PEER INFLUENCERS
* Young men and women aged between 15 and 19
* Living in La Réunion or Guadeloupe
* Enrolled in one of the selected vocational high schools and whose school principal agrees to participate in the program
* Selected in seconde class and admitted to première class
* Have been chosen as a peer
* Have a sense of self-efficacy in the use of computers
* Have good communication skills
* Possession of a video-capable smartphone
* Having agreed to take part in the study
* Written consent from a parent or guardian
Exclusion Criteria:
\- Involved in other similar programs
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Feasibility of the contraceptive education program, measured by the commitment rate of peer influencers.
Timeframe: From date of enrollment until the end of the programm and its evaluation, assessed up to 15 months
Trial details
NCT IDNCT06943209
SponsorCentre Hospitalier Universitaire de la Réunion