Text Messaging Program for Pregnancy Health
Trial Summary
What is the purpose of this trial?
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.
Will I have to stop taking my current medications?
The trial does not specify whether you need to stop taking your current medications. However, if you have health conditions that require individualized care, you may not be eligible to participate.
What data supports the effectiveness of the text messaging treatment for pregnancy health?
Research shows that text messaging can effectively promote various health behaviors, such as smoking cessation and medication adherence, which suggests it could be beneficial for pregnancy health. Additionally, the SmartMom program is endorsed by the Society of Obstetricians and Gynaecologists of Canada, indicating its credibility as a prenatal education tool.12345
Is the SmartMom text messaging program safe for pregnant women?
How is the Text Messaging Program for Pregnancy Health different from other treatments for pregnancy health?
The Text Messaging Program for Pregnancy Health is unique because it uses mobile health (mHealth) technology to deliver prenatal education through text messages, making it accessible and cost-effective, especially for those in rural or remote areas. Unlike traditional prenatal classes, this program can overcome barriers such as location, cost, and availability of instructors, and it is endorsed by the Society of Obstetricians and Gynaecologists of Canada.12456
Research Team
Patti Janssen, PhD
Principal Investigator
University of British Columbia
Eligibility Criteria
This trial is for pregnant individuals in Canada (except British Columbia) who are at or before 15 weeks gestation with a single pregnancy. They must be able to read and understand English at an 8th-grade level and be comfortable completing online surveys.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Intervention
Participants receive text messages promoting healthy behaviours during pregnancy
Control
Participants receive general interest messages on pregnancy-related topics
Follow-up
Participants are monitored for maternal, fetal, and newborn outcomes post-birth
Treatment Details
Interventions
- Control text messaging
- SmartMom text messaging
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of British Columbia
Lead Sponsor
Canadian Institutes of Health Research (CIHR)
Collaborator