Implementing a Novel Consent Process for Biospecimen Research After Newborn Screening
Eligible age
18+ yrs
Accepts
All genders
Locations
1 state
Healthy volunteers
Yes
See if you qualify for this study
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About this study
The purpose of this study is to implement an electronic consent education process for the retention and research use of residual dried bloodspots at four hospitals in Michigan and assess the impact of the new education, both on patients and hospital staff. The research team will recruit women who have just given birth to answer surveys about the Michigan BioTrust consent process. Surveys will be collected from participants in the hospital and again four weeks later. The research team will collect survey data from patient participants at each hospital prior to hospital staff implementation of the new education process and again after staff implementation.
Sponsor: Erin Rothwell
You may qualify if…
- ✓ Adult (\> 18 years)
- ✓ English, Spanish or Arabic speaking
- ✓ Just gave birth and currently a patient in the Mother \& Baby Unit in the hospital
You may not qualify if…
- ✕ Parents of infants who are born pre-term (\< 37 weeks gestation)
- ✕ Parents of infants in the Neonatal Intensive Care Unit
- ✕ Parents of infants being put up for adoption or in situations where legal guardianship is unknown at the time of birth
Where it's recruiting
Salt Lake City
Source: ClinicalTrials.gov · NCT06192511 · last updated 2026-07-31