Implementing a Novel Consent Process for Biospecimen Research After Newborn Screening
Recruiting
N/A
Interventional Study
Implementation Science
Informed Consent
Neonatal Screening
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.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Screening
- Participants needed
- 5,980 (estimated)
- Sponsor
- Erin Rothwell · Other
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About This Trial
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 c…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Adult (\> 18 years)
* English, Spanish or Arabic speaking
* Just gave birth and currently a patient in the Mother \& Baby Unit in the hospital
Exclusion Criteria:
* Parents of infants who are born pre-term (\< 37 weeks gestation)
* Parents of infants in the Neonatal Intensiv…
Contacts