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

Contraception Clinical Trial

— Mobile WACh XY  

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02781714
• Other study ID #: 51125
• Status: Completed
• Phase: N/A
• Start date: July 2016
• Est. completion date: September 2017

Study information

• Verified date: April 2018
• Source: University of Washington
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 260
• Est. completion date: September 2017
• Est. primary completion date: September 2017
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 14 Years to 50 Years

Eligibility

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

Related Conditions & MeSH terms

• Contraception
• Postpartum Period

Intervention

Behavioral:
• Two-way SMS
SMS messages will provide tailored and actionable education, counseling, and reminders specific to antenatal/postpartum timing and partner track. Messages will include questions and prompts; women and their male partners have the option of writing back to a nurse with questions or concerns, who will provide real-time responses via text and/or make referrals to a clinic. Message content will be tailored to women and couples, and will range from health benefits of child spacing and an emphasis on contraceptive options, to the hierarchy of effectiveness and information on specific methods, to simple reminders about postpartum visits. Prior to randomization, each enrolled woman will be asked if she has a male partner, and whether she would like to refer her male partner for recruitment and enrollment into the study. The partner tracks are as follows: Male partner invited to enroll/enrolled Male partner not invited to enroll Unpartnered

Locations

Country	Name	City	State
Kenya	Ahero sub-County Hospital	Ahero	Kisumu County
Kenya	Bondo County Hospital	Bondo	Siaya County

Sponsors (3)

Lead Sponsor	Collaborator
University of Washington	Kenyatta National Hospital, University of Nairobi

Country where clinical trial is conducted

Kenya, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Highly-effective contraceptive use	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.	6 months postpartum
Secondary	Time to contraceptive use	Time postpartum at which contraceptive use was initiated	Through study completion (6 months postpartum)
Secondary	Dual contraceptive use	Percentage of sexual acts in which a condom was used among contraceptive users	6 weeks, 14 weeks, and 6 months postpartum
Secondary	Any contraceptive use	Proportion of participants self-reporting use of any contraceptive method will be compared between arms. This outcome will be assessed with a questionnaire.	6 weeks, 14 weeks, and 6 months postpartum
Secondary	Family planning satisfaction questionnaire	Satisfaction with chosen contraceptive method	6 weeks, 14 weeks, and 6 months postpartum
Secondary	Exclusive breastfeeding questionnaire	Self-reported exclusive breastfeeding	6 weeks, 14 weeks, and 6 months postpartum