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NCT06192511 · ClinicalTrials.gov registry record · NA

Implementing a Novel Consent Process for Biospecimen Research After Newborn Screening

A NA study of Implementation Science and Informed Consent, sponsored by Erin Rothwell.

Recruiting
Registry status
NA
Development phase
5,980
Enrollment target
2
Study locations

NCT06192511 is a NA study of Implementation Science and Informed Consent that is actively recruiting participants, run by Erin Rothwell. The registered enrollment target is 5,980 participants, above the 1,284-participant average among 13 other Implementation Science trials with a reported enrollment target (366% higher). The trial reports 2 study locations across 1 state.

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The verdict

NCT06192511, a NA study of Implementation Science and Informed Consent, is actively recruiting participants, sponsored by Erin Rothwell.

RECRUITING
Registry status
NA
Development phase
5,980 participants
Enrollment target
2
Study locations

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.

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

FieldValue
Enrollment Target 5,980 participants
Start Date 2024-05-15
Est. Completion 2028-04-30
Phase NA

Sponsor

Erin Rothwell

2 total trials

What the Registry Record Tells You About NCT06192511

The ClinicalTrials.gov registry entry for NCT06192511 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 5,980 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 1,284-participant average among 13 other Implementation Science trials with a reported enrollment target (366% higher). The listed sponsor is Erin Rothwell, which has 2 total studies on file at ClinicalTrials.gov.

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.

NCT06192511 reports 2 study locations spanning 1 distinct geographic area - top geographies include Utah.

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.

What interventions are being tested in trial NCT06192511?

The interventions under investigation include: Educational Website and Video (BEHAVIORAL).

Who is sponsoring clinical trial NCT06192511?

This trial is sponsored by Erin Rothwell, which has 2 total clinical trials registered on ClinicalTrials.gov.

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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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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