Project HOPE 1000: Outcomes Related to Pregnancy

  • STATUS
    Recruiting
  • participants needed
    1000
  • sponsor
    Duke University
Updated on 19 February 2024

Summary

The purpose of this study is to collect biological samples from pregnant women and their babies and to collect data on long-term health, school outcomes, and the use of state and county services. The information we learn by doing this study may help identify important factors that may influence the health of mothers and babies, both short-and long-term.

Details
Condition Gravida
Age 18years - 100years
Clinical Study IdentifierNCT04417283
SponsorDuke University
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

The subject has provided a signed Informed consent prior to any study procedures
Maternal age at consent of 18 years old
Ability to understand English or Spanish
Willingness to comply with and be available for all protocol procedures
Singleton gestation < 24 weeks 0 days
Receiving prenatal care at a Duke-affiliated Obstetrics clinic with the intent of delivering at Duke University Health System-affiliated hospital (including Duke University Hospital and Duke Regional Hospital)
Plans to have their infant seen at a Duke-affiliated Pediatrics practice after birth
Plans to remain in the area for two years after delivery

Exclusion Criteria

Non-viable pregnancy
Having any condition that, in the opinion of the site investigators, would place the subject at unacceptable risk of injury or confound data interpretation
Clear my responses

How to participate?

Step 1 Connect with a study center
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

First name*
Last name*
Email*
Phone number*
Other language

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If 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 more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.