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An Intervention Delivered by App Instant Messaging to Increase Use of Effective Contraception Among Young Women in Bolivia

Not Applicable
Completed
Conditions
Contraception
Interventions
Other: Mobile phone app
Behavioral: Contraceptive instant messages
Registration Number
NCT02905526
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 use of effective contraception in Bolivia. Woman aged 16-24 will be randomised to have access to Centro de Investigacion, Educacion y Servicios'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 month follow-up.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
645
Inclusion Criteria
  • Aged 16-24
  • Own a personal Android mobile phone
  • Live in El Alto or La Paz Bolivia
  • Sexually active
  • Not using the pill, implant, injection, intrauterine device or patch
  • Want to avoid a pregnancy
Exclusion Criteria
  • Cannot read Spanish

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
ControlMobile phone appApp only
InterventionContraceptive instant messagesApp plus the contraceptive instant messages
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, patch)

Use of effective contraception4 months

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

Secondary Outcome Measures
NameTimeMethod
Service uptake4 months

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

Acceptability of individual effective contraceptive methods4 months

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

Discontinuation of effective contraception4 months

The proportion reporting use of effective contraception at any time during the 4 months (pill, intrauterine device, injection, implant, patch)

Unintended pregnancy4 months

The proportion reporting that they became pregnant and did not want to become pregnant during the study

Induced abortion4 months

The proportion reporting having an abortion during the study

Trial Locations

Locations (1)

Centro de Investigacion, Educacion y Servicios

🇧🇴

La Paz, Bolivia

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