Project for Reproductive Equity Through Volunteers and Entrepreneurship, Networks and Technology

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age15-19
SponsorDr. Karen Yeates

About this trial

The PREVENT Project is a multifaceted, adolescent friendly, culturally competent program aimed to address the issues surrounding unplanned pregnancies and lack of access and uptake of contraceptive services among adolescent girls. The intervention uses a mobile platform that provides educational SMS (Short Message Service) messaging, interactive voice response, and connects adolescent girls to community based AFSRH (Adolescent Friendly Sexual Reproductive Health) counselling services, as well as discreet contraceptive access points headed by female entrepreneurs. The program will be piloted for 12 months in various wards and villages in rural and urban Kilimanjaro, Tanzania.The acceptability and practicality of the intervention will be assessed using mixed methods. Questionnaires and focus groups will be conducted with the study participants, as well as the medical and non-medical volunteers at the start and end of the pilot. The study will be heavily supported by all-female non-medical social entrepreneurs and sexual reproductive health community mentors (volunteers), and, all-female medical reproductive health team. Recruitment will also take place in hair saloons (local hair braiding and styling establishments) and other female run business such as tailors and female clothing stores that have enlisted to become contraceptive access points in the study. There will be 2 intervention groups, control and case group. Both groups will receive educational SMS (text) messages on SRH (Sexual Reproductive Health) and access individually tailored educational resources through interactive voice response (IVR) services/system via PREVENT mobile platform. In addition to personal support to be able to contact with a SRH community peer mentor in the community for AFSRH counselling and support. The case group will then have access to contraception provided with detailed and discreet information on accessing PREVENT contraceptive access points in all communities included in the study.

Eligibility criteria

Qualifiers

Women 15-19 years of age

Reside within the study area for the duration of the study

Have a personal mobile phone and be willing to provide the phone number to the researchers to receive the intervention messages

Report being SMS literate (ie. able to read text messages in English or Swahili)

Disqualifiers

Be pregnant or planning pregnancy within 12 months (assessed when obtaining consent using HCG (human chorionic gonadotropin) urine dipstick).

Participation in another study or intervention that may affect the outcome of this study

Already utilizing a long-term form of contraception such as intra-uterine device, or implantable or inject-able contraception

Having a non-medical condition detected through screening that hinders study participation such as developmental or cognitive delay

Trial design

Treatments tested in this trial

  • Education
  • Personal Support
  • Access to contraception

Treatment groups

198 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Dr. Karen Yeates

Lead sponsor

Queen's University

Sponsor institution