MedPath

An Intervention Delivered by Text Message to Increase the Acceptability of Effective Contraception Among Young Women in Palestine

Not Applicable
Completed
Conditions
Contraception
Interventions
Behavioral: Contraceptive text messages
Other: Text messages not about contraception
Registration Number
NCT02905461
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 text message on the acceptability of effective contraception in Palestine. Woman aged 18-24 will be randomised to receive 0-3 text messages a day for 4 months (intervention) or a monthly text message not about contraception (control). Participants will complete a questionnaire at baseline and 4 month follow-up.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
586
Inclusion Criteria
  • Aged 18-24 years
  • Own a personal mobile phone
  • Not using the pill, implant, injection, intrauterine device or patch
  • Live in the West Bank
Exclusion Criteria
  • Cannot read Arabic

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
InterventionContraceptive text messagesContraceptive text messages
ControlText messages not about contraceptionText messages not about contraception
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)

Secondary Outcome Measures
NameTimeMethod
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

Use of effective contraception4 months

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

Induced abortion4 months

The proportion reporting having an abortion during the study

Service uptake4 months

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

Trial Locations

Locations (1)

Palestinian Family Planning and Protection Association

🇵🇸

Jerusalem, Palestinian Territory, occupied

© Copyright 2025. All Rights Reserved by MedPath