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
1 other identifier
interventional
580
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Nov 2016
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 14, 2016
CompletedFirst Posted
Study publicly available on registry
September 19, 2016
CompletedStudy Start
First participant enrolled
November 16, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 31, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
November 30, 2017
CompletedFebruary 7, 2018
September 1, 2017
9 months
September 14, 2016
February 6, 2018
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Acceptability of at least one method of effective contraception
The proportion reporting that at least one method of effective contraception is acceptable (pill, intrauterine device, injection, implant)
4 months
Secondary Outcomes (6)
Use of effective contraception
4 months
Acceptability of individual effective contraceptive methods
4 months
Discontinuation of effective contraception
4 months
Service uptake
4 months
Unintended pregnancy
4 months
- +1 more secondary outcomes
Other Outcomes (5)
Knowledge of effective contraception
4 months
Perceived norms in relation to using and communicating with partners about contraception
4 months
Personal agency in using (women only) and communicating with partners about contraception
4 months
- +2 more other outcomes
Study Arms (2)
Intervention
EXPERIMENTALApp plus the contraceptive instant messages
Control
PLACEBO COMPARATORApp only
Interventions
Eligibility Criteria
You may qualify if:
- Aged 16-24
- Own a personal Android mobile phone
- Live in Tajikistan
You may not qualify if:
- Cannot read Tajik or Russian
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Tajik Family Planning Alliance
Dushanbe, Tajikistan
Related Publications (3)
Palmer MJ, Henschke N, Villanueva G, Maayan N, Bergman H, Glenton C, Lewin S, Fonhus MS, Tamrat T, Mehl GL, Free C. Targeted client communication via mobile devices for improving sexual and reproductive health. Cochrane Database Syst Rev. 2020 Jul 14;8(8):CD013680. doi: 10.1002/14651858.CD013680.
PMID: 32779730DERIVEDMcCarthy O, Ahamed I, Kulaeva F, Tokhirov R, Saibov S, Vandewiele M, Standaert S, Leurent B, Edwards P, Palmer M, Free C. A randomized controlled trial of an intervention delivered by mobile phone app instant messaging to increase the acceptability of effective contraception among young people in Tajikistan. Reprod Health. 2018 Feb 13;15(1):28. doi: 10.1186/s12978-018-0473-z.
PMID: 29433506DERIVEDMcCarthy O, Leurent B, Edwards P, Tokhirov R, Free C. A randomised controlled trial of an intervention delivered by app instant messaging to increase the acceptability of effective contraception among young people in Tajikistan: study protocol. BMJ Open. 2017 Sep 21;7(9):e017606. doi: 10.1136/bmjopen-2017-017606.
PMID: 28939582DERIVED
Study Officials
- PRINCIPAL INVESTIGATOR
Caroline Free, PhD
London School of Hygiene and Tropical Medicine
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 14, 2016
First Posted
September 19, 2016
Study Start
November 16, 2016
Primary Completion
July 31, 2017
Study Completion
November 30, 2017
Last Updated
February 7, 2018
Record last verified: 2017-09