Mobile app support for at-risk mothers during pregnancy and postpartum
Supporting At-Risk Mothers Across Perinatal Period: A Randomized Controlled Trial
NA · National University of Singapore · NCT06363019
This study tests if a mobile app can help at-risk mothers during pregnancy and after childbirth by providing support and information, and compares their experiences to those getting regular care.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 200 (estimated) |
| Ages | 21 Years to 65 Years |
| Sex | Female |
| Sponsor | National University of Singapore (other) |
| Locations | 2 sites (Singapore and 1 other locations) |
| Trial ID | NCT06363019 on ClinicalTrials.gov |
What this trial studies
This interventional study evaluates the effectiveness of the SMART mobile application, designed to support at-risk mothers during the perinatal period. The app provides educational materials, peer support chat functions, and forums for interaction among mothers. Researchers will compare outcomes for mothers using the app with those receiving standard care, focusing on maternal mental health, parenting self-efficacy, and infant development. The study aims to assess both the effectiveness and cost-effectiveness of this mobile health intervention.
Who should consider this trial
Good fit: Ideal candidates are mothers aged 21 to 65 from vulnerable populations who can read and speak English and have access to a smartphone.
Not a fit: Patients with chronic physical or mental disorders that interfere with participation may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly improve mental health outcomes for mothers and developmental outcomes for infants.
How similar studies have performed: Other studies have shown promise in using mobile health interventions for maternal and infant health, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * mothers who (1) are 21 years old to 65 years old; (2) can read and speak English; (3) belong to a vulnerable population due to one or more of the following criteria: i) monthly household income is =/less than SGD 2500 and/or under any low-income support services (referral from social workers) ii) have positive maternal Adverse Childhood Events (ACES) evaluation; iii) single mother; iv) clinically referred by medical professionals or other allied workers for requiring psychosocial support; v) pregnancy or birth of baby diagnosed with congenital malformation/abnormality where baby is 1 year old or less and can be discharged home with mother; vi) mothers with Edinburgh Postnatal Depression Scores (EPDS) =9 (at-risk for depression); and (4) have a smartphone with internet access. Exclusion Criteria: * mothers who (1) have chronic physical or mental disorders which would interfere with their ability to participate in the study, and/or (2) gave birth to a baby who needs prolonged hospitalization or NICU support and /or stillborn (3) has a cognitive impairment
Where this trial is running
Singapore and 1 other locations
- Alice Lee Centre for Nursing Studies, National University of Singapore — Singapore, Singapore (RECRUITING)
- National University of Singapore — Singapore, Singapore (RECRUITING)
Study contacts
- Principal investigator: Shefaly Shorey, PhD — National University of Singapore
- Study coordinator: Shefaly Shorey, PhD
- Email: nurssh@nus.edu.sg
- Phone: 66011294
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Perinatal Depression, Parents, Anxiety, Self Efficacy, Stress, Infant Development