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

A Randomised Controlled Trial of an Intervention Delivered by App Instant Messaging to Increase the Acceptability of Effective Contraception Among Young People in Tajikistan

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02905513
Enrollment
580
Registered
2016-09-19
Start date
2016-11-16
Completion date
2017-11-30
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 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.

Interventions

BEHAVIORALContraceptive app instant messages

Sponsors

International Planned Parenthood Federation
CollaboratorOTHER
Tajik Family Planning Alliance
CollaboratorUNKNOWN
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
ALL
Age
16 Years to 24 Years
Healthy volunteers
Yes

Inclusion criteria

* Aged 16-24 * Own a personal Android mobile phone * Live in Tajikistan

Exclusion criteria

* Cannot read Tajik or Russian

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)

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)
Use of effective contraception4 monthsThe proportion reporting current use of effective contraception (pill, intrauterine device, injection, implant)
Discontinuation of effective contraception4 monthsThe 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 monthsThe proportion reporting attending a sexual health service during the 4 months
Unintended pregnancy4 monthsThe proportion reporting that they became pregnant (or partner became pregnant) and did not want to become pregnant during the study
Induced abortion4 monthsThe proportion reporting having (or partner having) an abortion during the study

Other

MeasureTime frameDescription
Personal agency in using (women only) and communicating with partners about contraception4 monthsResponses to the personal agency scales
Intention to use effective contraception (women only)4 monthsScore on the intention measure
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

Countries

Tajikistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026