POWERMOM, A Healthy Pregnancy Research Community
1 other identifier
observational
100,000
1 country
1
Brief Summary
This study will take advantage of the open source framework of ResearchKit developed by Apple to bring research directly to participants. Using the ResearchKit platform as well as a stand alone app available for Android and HTML, it makes it easier to enroll large numbers of participants and carry out real-world health research to answer questions important to a broad population.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Mar 2017
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 6, 2017
CompletedStudy Start
First participant enrolled
March 16, 2017
CompletedFirst Posted
Study publicly available on registry
March 21, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 13, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 31, 2027
April 17, 2024
April 1, 2024
10 years
March 6, 2017
April 15, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Improve our understanding of healthy pregnancy weight gain for all women.
Weight (lbs.) will be collected using surveys and measured with home and medical office scales.
Up to 46 weeks.
Improve our understanding of how different factors impact pregnancy complications.
Pregnancy complications will be collected using surveys.
Up to 46 weeks.
Improve our understanding how different factors impact the birth of the baby.
Birth outcomes will be collected using surveys.
Up to 46 weeks.
Eligibility Criteria
Pregnant women, 16 years or older, who currently live in the United States, and own a smartphone.
You may qualify if:
- 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
You may not qualify if:
- Inability to consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Scripps Research Translational Institute
La Jolla, California, 92037, United States
Related Publications (1)
Ajayi T, Kueper J, Ariniello L, Ho D, Delgado F, Beal M, Waalen J, Baca Motes K, Ramos E. Digital Health Platform for Maternal Health: Design, Recruitment Strategies, and Lessons Learned From the PowerMom Observational Cohort Study. JMIR Form Res. 2025 Apr 7;9:e70149. doi: 10.2196/70149.
PMID: 40194282DERIVED
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Lase Ajayi, MD
The Scripps Research Institute
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 6, 2017
First Posted
March 21, 2017
Study Start
March 16, 2017
Primary Completion (Estimated)
March 13, 2027
Study Completion (Estimated)
July 31, 2027
Last Updated
April 17, 2024
Record last verified: 2024-04