Home › NCT07557303
Supporting Just-In-Time Consent for Prenatal Screening: The INFORM Study
Who can join
Ages 18 and older · Women · Healthy volunteers welcome
Full eligibility criteria
Inclusion Criteria: * Currently pregnant and receiving care at a participating collaborative site - University of North Carolina, Chapel Hill; Zuckerberg Chan San Francisco General Hospital; University of Florida Health, Jacksonville. * 18 years of age and older * Able to read, speak, and understand English or Spanish * Has not previously been offered prenatal genetic screening for the current pregnancy * 24 weeks (6 months) gestational age or less Exclusion Criteria: * Not pregnant, not a patient at a partner clinical site * Younger than 18 years of age * Not being able to read, speak, and understand English or Spanish * Has previously been offered prenatal genetic screening for the current pregnancy * Greater than 24 weeks gestational age (6 months)
About the study
This clinical trial is about prenatal genetic screening. It will test an intervention to help people make decisions about screening. The intervention is a short set of information cards about screening. This intervention is for pregnant participants. They will use the intervention on their mobile phone before they see their doctor.
The study has one main question:
* Do participants who use the intervention feel more confident when they make a decision about screening?
Researchers will compare participants who use the intervention to participants who do not. All participants will have their usual care when they visit their doctor.
What will participants do?
* Participants must be pregnant. They will sign up for the study before their first doctor's visit for their pregnancy. This is the visit where their doctor usually talks with them about screening. * Some participants will use the intervention before their first doctor's visit. Other participants will not use it. * All participants will talk with a researcher on the phone after their first doctor's visit. * Participants who use the intervention will answer a short survey on their phone. * A few participants who use the intervention will talk with a researcher a second time on the phone.
What is being tested
- Mobile-based Educational Intervention (behavioral)
Sponsor: Case Western Reserve University · Participants: 1,400 · Started: Sep 10, 2026
Contact the study team
- Sabina Rubeck, MPH · Phone: 216-368-2547
- Harlie Custer, MA, MPH · Phone: (216) 368-5914
Official record on ClinicalTrials.gov — NCT07557303
Locations in the U.S.
| California | Zuckerberg Chan San Francisco General Hospital, San Francisco |
| Florida | University of Florida Health, Jacksonville |
| North Carolina | University of North Carolina, Chapel Hill |
From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.