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Mobile Phone Messaging to Improve Women's and Children's Health (Mobile WACh) in Kenya

Mobile Phone One Way Short Message Service (SMS) Versus SMS Dialogue for Women's and Child Health (Mobile WACh) in Kenya: A Randomized Control Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01894126
Acronym
Mobile WACh
Enrollment
300
Registered
2013-07-09
Start date
2013-07-31
Completion date
Unknown
Last updated
2016-11-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Family Planning, Maternal Health, Neonatal Health

Brief summary

With the increased prevalence of cellular phones, mobile technology provides an important tool to reach underserved populations in low to middle income countries. mHealth interventions offer promise to improve maternal child health throughout the reproductive health continuum if they contribute to increasing skilled birth attendance, family planning and exclusive breastfeeding. We propose a randomized clinical trial to determine effect of using mobile phones to deliver SMS (one-way) versus an interactive SMS dialogue (two-way) on uptake of reproductive and neonatal health services and maternal and infant outcomes

Interventions

BEHAVIORALTwo-way SMS Dialogue
BEHAVIORALOne-way SMS Messaging

Sponsors

National Institutes of Health (NIH)
CollaboratorNIH
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
CollaboratorNIH
University of Nairobi
CollaboratorOTHER
Kenyatta National Hospital
CollaboratorOTHER_GOV
University of Washington
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
14 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Pregnant * Access to a mobile phone * Able to read SMS messages * Willing to receive SMS messages

Exclusion criteria

* Unwilling or unable to meet inclusion criteria

Design outcomes

Primary

MeasureTime frame
Contraceptive uptake10 weeks postpartum; 24 weeks postpartum
Facility DeliveryPostpartum
Exclusive Breastfeeding24 weeks postpartum

Secondary

MeasureTime frame
ANC attendancePostpartum
Infant mortalitySix months postpartum
Infant ImmunizationsSix months postpartum
Maternal mortality6 months postpartum

Countries

Kenya

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026