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

A Randomised Controlled Trial of an Intervention Delivered by Text Message to Increase the Acceptability of Effective Contraception Among Young Women in Palestine

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02905461
Enrollment
586
Registered
2016-09-19
Start date
2016-12-08
Completion date
2018-01-31
Last updated
2018-02-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Contraception

Keywords

Reproductive health

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.

Interventions

BEHAVIORALContraceptive text messages
OTHERText messages not about contraception

Sponsors

Palestinian Family Planning and Protection Association
CollaboratorOTHER
International Planned Parenthood Federation
CollaboratorOTHER
London School of Hygiene and Tropical Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 24 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Acceptability of at least one method of effective contraception4 monthsThe proportion reporting that at least one method of effective contraception is acceptable (pill, intrauterine device, injection, implant, patch)

Secondary

MeasureTime frameDescription
Acceptability of individual effective contraceptive methods4 monthsThe proportion reporting that individual methods of effective contraception are acceptable (pill, intrauterine device, injection, implant, patch)
Use of effective contraception4 monthsThe proportion reporting current use of effective contraception (pill, intrauterine device, injection, implant, patch)
Discontinuation of effective contraception4 monthsThe proportion reporting use of effective contraception at any time during the 4 months (pill, intrauterine device, injection, implant, patch)
Service uptake4 monthsThe proportion reporting attending a sexual health service during the 4 months
Unintended pregnancy4 monthsThe proportion reporting that they became pregnant and did not want to become pregnant during the study
Induced abortion4 monthsThe proportion reporting having an abortion during the study

Other

MeasureTime frameDescription
Intervention 'dose' received4 monthsIf participants read all, some, most or none of the messages and if they stopped the messages
Perceived norms in relation to using and communicating with partners about contraception4 monthsResponses to the perceived norms scales
Knowledge of effective contraception4 monthsScore on the knowledge measure
Intention to use effective contraception4 monthsResponse to the intention scale
Personal agency in using and communicating with partners about contraception4 monthsResponses to the personal agency scales

Countries

Palestinian Territories

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026