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Completed

NCT Number: NCT02905513

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

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.

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Key information

Conditions

Contraception

Age range

16 year–24 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Tajik Family Planning Alliance

Dushanbe, Tajikistan

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • Cannot read Tajik or Russian

Treatment and study plan

Contraceptive app instant messages

Behavioral

Mobile phone app

Other

Primary outcomes

  1. Acceptability of at least one method of effective contraception

    Time frame: 4 months

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

Secondary outcomes

  1. Use of effective contraception

    Time frame: 4 months

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

  2. Acceptability of individual effective contraceptive methods

    Time frame: 4 months

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

  3. Discontinuation of effective contraception

    Time frame: 4 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)

  4. Service uptake

    Time frame: 4 months

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

  5. Unintended pregnancy

    Time frame: 4 months

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

  6. Induced abortion

    Time frame: 4 months

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

Other outcomes

  1. Knowledge of effective contraception

    Time frame: 4 months

    Score on the knowledge measure

  2. Perceived norms in relation to using and communicating with partners about contraception

    Time frame: 4 months

    Responses to the perceived norms scales

  3. Personal agency in using (women only) and communicating with partners about contraception

    Time frame: 4 months

    Responses to the personal agency scales

  4. Intention to use effective contraception (women only)

    Time frame: 4 months

    Score on the intention measure

  5. Intervention 'dose' received

    Time frame: 4 months

    If participants read all, some, most or none of the messages and if they stopped the messages

Sponsors and collaborators

Lead sponsor

London School of Hygiene and Tropical Medicine

Other

Collaborators

  • International Planned Parenthood Federation
  • Tajik Family Planning Alliance

Registry information

Official study title

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

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Sep 19, 2016
Registry last updated
Feb 7, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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