Assessing the Safety of Pregnancy In the CoRonavirus (COVID-19) pandEmic
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- STATUS
- Recruiting
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- participants needed
- 11000
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- sponsor
- University of California, San Francisco
Summary
Prospective nationwide cohort study of pregnant women enrolled early in gestation and followed for Covid-19 exposure and infection, with follow up of obstetrical outcomes and infant development through the first year of life.
Description
ASPIRE is focused on the first trimester, a critical and vulnerable period when all of a baby's organ systems form and the placenta - the crucial connection between mom and baby - develops.
Currently, there are no data about the effects of COVID-19 infections in the first trimester. The study will provide critical information to:
- Guide the care of pregnant women
- Protect the safety of their babies and families
- Help those considering pregnancy in the future understand what it means to be pregnant in this new era
The investigators are recruiting 10,000 women from the start of pregnancy and will track COVID-19 exposures using frequent serology testing. The investigators will collect information during and after the pregnancy to try to determine the effects of COVID 19 for mom and baby.
Participants will be asked to do the following throughout pregnancy:
- Submit frequent, quick (<1 minute each) symptom tracking reports using your mobile phone and/or computer.
- Collect finger-stick blood samples from home at several points throughout your pregnancy.
- Give permission to review medical records related to your pregnancy, delivery and baby's development.
- Complete questionnaires online about your health during your pregnancy and after delivery of your baby.
Details
| Condition | Pregnancy Related, COVID, Corona Virus Infection, Early Pregnancy |
|---|---|
| Age | 18years - 100years |
| Clinical Study Identifier | NCT04388605 |
| Sponsor | University of California, San Francisco |
| Last Modified on | 19 February 2024 |
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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