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Implementing a Novel Consent Process for Biospecimen Research After Newborn Screening
NCT06192511 · View on ClinicalTrials.gov ↗
Study Summary
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.
Conditions Studied
Interventions
- BEHAVIORAL Educational Website and Video
Study Locations (2)
Utah
- University of Utah Hospital and Clinics — Salt Lake City
- University of Utah, Department of Obstetrics & Gynecology — Salt Lake City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 5,980 participants |
| Start Date | 2024-05-15 |
| Est. Completion | 2028-04-30 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06192511
The ClinicalTrials.gov registry entry for NCT06192511 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 5,980 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Erin Rothwell, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with Implementation Science appearing as the primary indexed condition, and to 1 intervention — of which Educational Website and Video is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06192511 reports 2 study locations spanning 1 distinct geographic area — top geographies include Utah. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06192511 about?
NCT06192511 is a clinical study titled "Implementing a Novel Consent Process for Biospecimen Research After Newborn Screening". 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 ha...
What is the current status of trial NCT06192511?
This trial is currently recruiting. It is a NA study. The enrollment target is 5,980 participants. The study started on 2024-05-15. Estimated completion is 2028-04-30.
What conditions does trial NCT06192511 study?
This clinical trial studies the following conditions: Implementation Science, Informed Consent, Neonatal Screening. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06192511?
The interventions under investigation include: Educational Website and Video (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06192511?
This trial is sponsored by Erin Rothwell, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06192511 being conducted?
This trial has 2 study locations across Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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