Mobile Health Intervention (Support-moms) in Antenatal Care to Improve Maternal Health in Uganda

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age10-65
SponsorMbarara University of Science and Technology

About this trial

High maternal mortality is a major public health problem in many settings. Because of low antenatal care (ANC) and skilled birth usage, Ugandan women and their children suffer from high maternal and perinatal mortality. The investigators developed a promising intervention (Support-Moms app) that shares targeted health information, and engages social support networks through scheduled reminders to help support pregnant women to utilize maternity services in rural Uganda. The investigators now propose to test and implement the Support-Moms intervention and hypothesize that Support-Moms will be feasible and cost-effective in improving utilization of available maternity care services, and ultimately reduce maternal and perinatal mortality.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

are in the first trimester of pregnancy who have not yet presented for ANC

reside in the catchment area of a study HC

are emancipated minors and adults aged ≥ 18 years

report access to a cell phone with reception in their home

Disqualifiers

do not own a cell phone for personal use with reported reliable reception

are unable to use SMS or unwilling to receive SMS notifications

are under 18 years of age

do not own a cell phone for personal use with reported reliable reception

Trial design

Design model

Parallel

Treatments tested in this trial

  • Support-Moms

    Behavioral

    Scheduled SMS-audio messages from the final messaging prototype (SM), plus social supporter engagement through SMS (SS).

  • Control

    Behavioral

    Routine care/ information giving

Treatment groups

1,680 Participants
are divided into 2 treatment groups
Group A: InterventionExperimental treatment 1 intervention
Group B: ControlActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Healthcare provider (HCP)-led skilled births

Proportion of individuals delivering with the help of a healthcare provider (HCP)

Time frame
15 months

Secondary outcomes

1

Maternal, implementation, service and client outcomes

Proportion of individuals who report the following outcomes: a) number of ANC visits, b) institution-based delivery, c) social support d) mode of infant delivery, e) all deaths (maternal, fetal, newborn), f) preterm birth, g) birth weight, h) breastfeeding, i) completion of post-natal care, j) complications of pregnancy and childbirth (e.g obstructed labor, ruptured uterus, need for neonatal or maternal resuscitation/ assisted ventilation, severe preeclampsia/ eclampsia, postpartum hemorrhage (PPH), maternal/newborn sepsis, and other infections); and implementation, service and client outcomes

Time frame
15 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Mbarara University of Science and Technology

Lead sponsor

University of Alabama at Birmingham

Collaborator

Harvard Medical School (HMS and HSDM)

Collaborator

Massachusetts General Hospital

Collaborator

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Collaborator