An Intervention Delivered by App Instant Messaging to Increase the Acceptability of Effective Contraception Among Young People in Tajikistan
- Conditions
- Contraception
- Interventions
- Behavioral: Contraceptive app instant messagesOther: Mobile phone app
- Registration Number
- NCT02905513
- Lead Sponsor
- London School of Hygiene and Tropical Medicine
- Brief Summary
This randomised controlled trial will establish the effect a contraceptive intervention delivered by mobile phone app instant messaging on the acceptability of effective contraception in Tajikistan. Woman and men aged 16-24 will be randomised to have access to the Tajik Family Planning Alliance's sexual and reproductive health app (control) or the app plus 0-3 instant messages a day for 4 months (intervention). Participants will complete a questionnaire at baseline and 4 months.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 580
- Aged 16-24
- Own a personal Android mobile phone
- Live in Tajikistan
- Cannot read Tajik or Russian
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Intervention Contraceptive app instant messages App plus the contraceptive instant messages Control Mobile phone app App only Intervention Mobile phone app App plus the contraceptive instant messages
- Primary Outcome Measures
Name Time Method Acceptability of at least one method of effective contraception 4 months The proportion reporting that at least one method of effective contraception is acceptable (pill, intrauterine device, injection, implant)
- Secondary Outcome Measures
Name Time Method Use of effective contraception 4 months The proportion reporting current use of effective contraception (pill, intrauterine device, injection, implant)
Induced abortion 4 months The proportion reporting having (or partner having) an abortion during the study
Acceptability of individual effective contraceptive methods 4 months The proportion reporting that individual methods of effective contraception are acceptable (pill, intrauterine device, injection, implant)
Unintended pregnancy 4 months The proportion reporting that they became pregnant (or partner became pregnant) and did not want to become pregnant during the study
Discontinuation of effective contraception 4 months The proportion reporting use (or partner's use) of effective contraception at any time during the 4 months (pill, intrauterine device, injection, implant, patch)
Service uptake 4 months The proportion reporting attending a sexual health service during the 4 months
Trial Locations
- Locations (1)
Tajik Family Planning Alliance
🇹🇯Dushanbe, Tajikistan