POWERMOM, A Healthy Pregnancy Research Community

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03085875

Enrollment

100000

Registered

2017-03-21

Start date

2017-03-16

Completion date

2027-07-31

Last updated

2024-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Behavior, Health Problems in Pregnancy, Pregnancy Related, Weight Change, Body

Keywords

Weight Change, Healthy Pregnancy, Physiologic Sensors

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.

Detailed description

* Eligibility determined, Individuals enrolled and consented to join study * Short Intake Survey (demographic and baseline health information collected) * Health History Survey (two days after participant enrolls in the study) * Survey questions about current health and medical history will be sent to participants weekly. If participants had a prenatal visit during the week, a few additional questions will be asked. * Twins / Multiples survey will begin appearing when a participant indicates they are having more than one baby * Participants can submit home measurements of, weight and blood pressure as frequently as they want through HealthKit. * Pregnancy outcome variables. (Miscarriage, stillbirth, birth of healthy baby, or pregnancy ended) will also be asked weekly. * If the baby is born, questions about labor and delivery, as well as weight, size and birth date of the baby will be asked. A reminder to fill out the outcome survey will be given 4 weeks after a user's due date.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

CROSS_SECTIONAL

Eligibility

Sex/Gender

FEMALE

Age

16 Years to No maximum

Healthy volunteers

Yes

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

Design outcomes

Primary

Measure	Time frame	Description
Improve our understanding of healthy pregnancy weight gain for all women.	Up to 46 weeks.	Weight (lbs.) will be collected using surveys and measured with home and medical office scales.
Improve our understanding of how different factors impact pregnancy complications.	Up to 46 weeks.	Pregnancy complications will be collected using surveys.
Improve our understanding how different factors impact the birth of the baby.	Up to 46 weeks.	Birth outcomes will be collected using surveys.

Countries

United States

Contacts

Primary ContactLase Ajayi, MD

tajayi@scripps.edu(858) 554-5734

Backup ContactLauren M Ariniello, BS

laurena@scripps.edu858-784-2253

Outcome results