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Evaluation of an mHealth SMS Dialogue Strategy to Meet Women's and Couples' Postpartum Contraceptive Needs in Kenya

Not Applicable
Completed
Conditions
Postpartum Period
Contraception
Interventions
Behavioral: Two-way SMS
Registration Number
NCT02781714
Lead Sponsor
University of Washington
Brief Summary

Meeting women's need for postpartum family planning is has been acknowledged as a global priority in maternal and child health. The prevention of unintended pregnancies in sub-Saharan African countries, which carry the highest global burdens of maternal mortality and HIV infection, is projected to substantially decrease maternal and neonatal morbidity and mortality. Many barriers to contraceptive uptake exist, both within and outside of the postpartum time period, and include socio-cultural, economic, and supply-side factors. Furthermore, while the importance of engaging men in family planning programs has been acknowledged for decades, few interventions have succeeded in increasing male involvement in family planning while maintaining a focus on women's empowerment. Innovative approaches to meeting the family planning needs of women and couples are urgently needed.

Public health interventions are increasingly incorporating mobile health (mHealth) approaches using short message service (SMS) technology in low-income countries, approaches that have demonstrated benefit among various reproductive health outcomes. The investigators hypothesize that personalized, bidirectional SMS dialogue with individual women and couples will increase postpartum contraceptive uptake, thereby decreasing unmet need for family planning in Kenya. The investigators have collaborated with the University of Washington (UW) Department of Computer Science and Engineering (CSE) along with Kenyan telecommunication providers to develop a hybrid messaging system that allows for innovative bidirectional SMS messaging. This system has been used successfully in maternal child health (MCH) clinics in Kenya. In qualitative research, women in Kenya have expressed a strong desire for mHealth support to provide additional education, counseling and reminders to supplement counseling by health workers.

The investigators propose a randomized controlled trial (RCT) comparing the effects of bidirectional SMS dialogue vs. control on highly effective contraceptive use at 6 months postpartum among HIV negative women and couples in Nyanza Province, Kenya. Data from this RCT and accompanying qualitative study will contribute to innovative, scale-able strategies to address unmet need for contraception and increase male involvement in family planning.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
260
Inclusion Criteria
  • Pregnant; at least 28 weeks gestation
  • HIV negative
  • Daily access to a mobile phone
  • Planning to stay in area for 6 months postpartum
  • Able to read/write or has trusted person to help
Exclusion Criteria
  • Does not meet above criteria

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Two-way SMSTwo-way SMSPre-programmed SMS messages by partner track will be delivered twice weekly to participants in participants' preferred languages from enrollment to 6 months postpartum. They will include a question soliciting a response from the participant(s). Interactive SMS communication will be responded to and managed by the study nurse at each site. Content themes will include: general support/encouragement, postpartum visit reminders, postpartum pregnancy risk and benefits of birth spacing, postpartum contraceptive options and side effects, family planning misconceptions, and couple communication.
Primary Outcome Measures
NameTimeMethod
Highly-effective contraceptive use6 months postpartum

Proportion of participants self-reporting use of oral contraceptive pills, injectable contraception, contraceptive implant, intrauterine device, or male/female sterilization at 6 months postpartum will be compared between arms. Questionnaires will be used to assess this outcome.

Secondary Outcome Measures
NameTimeMethod
Time to contraceptive useThrough study completion (6 months postpartum)

Time postpartum at which contraceptive use was initiated

Dual contraceptive use6 weeks, 14 weeks, and 6 months postpartum

Percentage of sexual acts in which a condom was used among contraceptive users

Any contraceptive use6 weeks, 14 weeks, and 6 months postpartum

Proportion of participants self-reporting use of any contraceptive method will be compared between arms. This outcome will be assessed with a questionnaire.

Family planning satisfaction questionnaire6 weeks, 14 weeks, and 6 months postpartum

Satisfaction with chosen contraceptive method

Exclusive breastfeeding questionnaire6 weeks, 14 weeks, and 6 months postpartum

Self-reported exclusive breastfeeding

Trial Locations

Locations (2)

Bondo County Hospital

🇰🇪

Bondo, Siaya County, Kenya

Ahero sub-County Hospital

🇰🇪

Ahero, Kisumu County, Kenya

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