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

Abroad (travel likely)Recruiting

Conditions

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

Simple summaryAI-assisted

This summary is produced by a language model and is experimental. It may be incomplete or inaccurate and is not a substitute for professional medical advice.

Locations

Zuckerberg Chan San Francisco General Hospital, San Francisco, California, United States
Contact: Study coordinator (Miriam Kuppermann, MPH, PhD) · miriam.kuppermann@ucsf.edu · 415-502-4089
Contact: Study coordinator (Kimberly Coleman-Phox, MPH) · kimberly.coleman-phox@ucsf.edu · 415-476-6406
University of Florida Health, Jacksonville, Florida, United States
Contact: Study coordinator (Niamh Condon, DO, FACOOG) · Niamh.Condon@jax.ufl.edu · 904-383-1037
Contact: Study coordinator (Julie Nowak) · julie.nowak@jax.ufl.edu
University of North Carolina, Chapel Hill, North Carolina, United States
Contact: Study coordinator (Neeta Vora, MD) · Neeta_vora@med.unc.edu · (984) 974-2131
Contact: Study coordinator (Amber Ivins, MSCR) · amber_ivins@med.unc.edu

Study leads

Marsha Michie, PhD
Principal Investigator
Case Western Reserve University
Megan Allyse, PhD
Principal Investigator
Case Western Reserve University

View source on ClinicalTrials.gov