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An Intervention Delivered by App Instant Messaging to Increase the Acceptability of Effective Contraception Among Young People in Tajikistan

Not Applicable
Completed
Conditions
Contraception
Interventions
Behavioral: Contraceptive app instant messages
Other: 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
Inclusion Criteria
  • Aged 16-24
  • Own a personal Android mobile phone
  • Live in Tajikistan
Exclusion Criteria
  • Cannot read Tajik or Russian

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
InterventionContraceptive app instant messagesApp plus the contraceptive instant messages
ControlMobile phone appApp only
InterventionMobile phone appApp plus the contraceptive instant messages
Primary Outcome Measures
NameTimeMethod
Acceptability of at least one method of effective contraception4 months

The proportion reporting that at least one method of effective contraception is acceptable (pill, intrauterine device, injection, implant)

Secondary Outcome Measures
NameTimeMethod
Use of effective contraception4 months

The proportion reporting current use of effective contraception (pill, intrauterine device, injection, implant)

Induced abortion4 months

The proportion reporting having (or partner having) an abortion during the study

Acceptability of individual effective contraceptive methods4 months

The proportion reporting that individual methods of effective contraception are acceptable (pill, intrauterine device, injection, implant)

Unintended pregnancy4 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 contraception4 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 uptake4 months

The proportion reporting attending a sexual health service during the 4 months

Trial Locations

Locations (1)

Tajik Family Planning Alliance

🇹🇯

Dushanbe, Tajikistan

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