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Clinical Trial Summary

The goal of this randomized clinical trial is to evaluate the effectiveness of SmartMom, a text messaging-based mobile health program for prenatal education. The main questions are to determine if healthy pregnant people receiving SmartMom messages that promote health behaviours in pregnancy versus messages that don't provoke behaviour change have improvement in: 1. knowledge about healthy pregnancy and birth 2. standardized measures of depression, anxiety, and fear of childbirth 3. adoption of positive health behaviours in pregnancy 4. maternal, fetal, and newborn outcomes Participants in the intervention group will receive three evidence-based text messages per week, plus optional supplemental messages on topics relevant to them, throughout pregnancy. The control group will receive general interest messages on pregnancy-related topics that are not promoting behaviour change.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05793944
Study type Interventional
Source University of British Columbia
Contact Sara Leckie, MSc
Phone 604-875-2345
Email sara.leckie@ubc.ca
Status Recruiting
Phase N/A
Start date November 10, 2023
Completion date February 2026

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