Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
University of Minnesota
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
A study participant can include a pregnant person past 20 weeks of pregnancy (this includes a vulnerable population)
Willing and able to comply with study procedures.
Participants must be ≥ 18 years old.
Participants must be able to read, write and speak English.
Participants must have access, and ability to use a smartphone, tablet, or computer in a private location.
The pregnant woman/person and her caregiving partner are planning for infant delivery and care.
The fetal diagnosis of the major anomaly affects the heart (i.e., CCHD). See definition of CCHD included earlier in the protocol. Other anomalies could be present and potentially impair other organs.
The infant's anomaly will likely require surgical and/or medical intervention within the first year of life.
The fetus/infant is expected to live with surgical and/or medical intervention (this includes a vulnerable population).
There may be genetic and/or chromosomal conditions in addition to the heart/structural anomalies
You may not be if
Pregnancy termination
The fetal anomaly diagnosis is highly likely to result in fetal or infant demise shortly after birth.
Adults lacking the capacity to consent
Adults who do not have access to a smart phone, tablet, or device.
Caregiving partner cannot enroll if mother is not enrolled
Clareo Health | Preparing Heart and Mind™: A Patient Engagement Pathway for Parents and Their Caregiving Partners After a Major Fetal Anomaly Diagnosis
