Supporting Just-In-Time Consent for Prenatal Screening: The INFORM Study

Recruiting N/A Interventional Study
Delivery of Health Care Genetic Testing Humans Pregnancy Noninvasive Prenatal Testing Informed Consent Internet-Based Intervention Self Efficacy Pregnant People Decision Making Health Education Patient Education as Topic/Method
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Female
Study type
Interventional
Purpose
Health Services Research
Participants needed
1,400 (estimated)
Sponsor
Case Western Reserve University · Other
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial
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 i…
Trial Locations
Loading…

Loading trial locations…

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 understan…
Contacts

Sabina Rubeck, MPH

216-368-2547

sabina.rubeck@case.edu

CONTACT

Harlie Custer, MA, MPH

(216) 368-5914

harlie.custer@case.edu

CONTACT