Research community for healthy pregnancies
POWERMOM, A Healthy Pregnancy Research Community
This study is trying to gather information from pregnant people about their health and experiences to better understand pregnancy outcomes and support healthy pregnancies.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100000 (estimated) |
| Ages | 16 Years and up |
| Sex | Female |
| Sponsor | Scripps Translational Science Institute Academic / other |
| Locations | 1 site (La Jolla, California) |
| Trial ID | NCT03085875 on ClinicalTrials.gov |
What this trial studies
This observational study utilizes the ResearchKit framework developed by Apple to engage participants in real-world health research focused on pregnancy. Participants will complete intake and health history surveys, and receive weekly questions about their health and prenatal visits. They can also submit home measurements like weight and blood pressure through HealthKit. The study aims to gather data on pregnancy outcomes and experiences, including labor and delivery details.
Who should consider this trial
Good fit: Ideal candidates include adults aged 16 and older who are currently pregnant or within 8 weeks postpartum and reside in the United States.
Not a fit: Patients who are unable to consent or do not have access to a smartphone or tablet may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into healthy pregnancy practices and outcomes, potentially improving maternal and infant health.
How similar studies have performed: Other studies utilizing mobile health technologies for pregnancy research have shown promise, indicating that this approach is both relevant and potentially impactful.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adults, 16 years of age or older * Pregnant women or within 8 weeks postpartum * Currently live within the United States * Own, and comfortable using, a smartphone or tablet Exclusion Criteria: • Inability to consent
Where this trial is running
La Jolla, California
- Scripps Research Translational Institute — La Jolla, California, United States (Recruiting)
Study contacts
- Principal investigator: Lase Ajayi, MD — The Scripps Research Institute
- Study coordinator: Lase Ajayi, MD
- Email: tajayi@scripps.edu
- Phone: (858) 554-5734
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.