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NCT06892275 · ClinicalTrials.gov registry record · NA
The FYI on MRI: A Multilevel Decision Support Intervention for Screening Breast MRI
A NA study of Magnetic Resonance Imaging and Breast Neoplasm Female, sponsored by Georgetown University.
- Recruiting
- Registry status
- NA
- Development phase
- 80
- Enrollment target
- 1
- Study location
NCT06892275 is a NA study of Magnetic Resonance Imaging and Breast Neoplasm Female that is actively recruiting participants, run by Georgetown University. The registered enrollment target is 80 participants, below the 154-participant average among 20 other Magnetic Resonance Imaging trials with a reported enrollment target (48% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06892275, a NA study of Magnetic Resonance Imaging and Breast Neoplasm Female, is actively recruiting participants, sponsored by Georgetown University.
- RECRUITING
- Registry status
- NA
- Development phase
- 80 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to test the impact of a multilevel decision support intervention on informed decisions about breast MRI among high-risk Black and Latina women. Participants (N=80) will be randomized to (1) enhanced usual care (risk assessment + referral to nurse practitioner) or (2) decision support (enhanced usual care + decision aid). Assessments will take place at baseline (T0) and 1-month post-intervention (T1). The primary outcome is informed decisions about breast MRI at T1.
Conditions Studied
Interventions
- BEHAVIORAL Enhanced Usual Care
- BEHAVIORAL Decision Support
Study Locations (1)
District of Columbia
- Georgetown University - Washington D.C.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 80 participants |
| Start Date | 2025-06-01 |
| Est. Completion | 2027-12 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06892275
The ClinicalTrials.gov registry entry for NCT06892275 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 154-participant average among 20 other Magnetic Resonance Imaging trials with a reported enrollment target (48% lower). The listed sponsor is Georgetown University, which has 227 total studies on file at ClinicalTrials.gov.
The record links to 4 conditions, with Magnetic Resonance Imaging appearing as the primary indexed condition, and to 2 interventions - of which Enhanced Usual Care is the first listed.
NCT06892275 reports 1 study location spanning 1 distinct geographic area - top geographies include District of Columbia.
Frequently Asked Questions
What is clinical trial NCT06892275 about?
NCT06892275 is a clinical study titled "The FYI on MRI: A Multilevel Decision Support Intervention for Screening Breast MRI". The purpose of this study is to test the impact of a multilevel decision support intervention on informed decisions about breast MRI among high-risk Black and Latina women. Participants (N=80) will be randomized to (1) enhanced usual care (risk assessment + referral to nurse practitioner) or (2) dec...
What is the current status of trial NCT06892275?
This trial is currently recruiting. It is a NA study. The enrollment target is 80 participants. The study started on 2025-06-01. Estimated completion is 2027-12.
What conditions does trial NCT06892275 study?
This clinical trial studies the following conditions: Magnetic Resonance Imaging, Breast Neoplasm Female, Early Detection of Cancer, Hereditary Breast and Ovarian Cancer Syndrome.
What interventions are being tested in trial NCT06892275?
The interventions under investigation include: Enhanced Usual Care (BEHAVIORAL), Decision Support (BEHAVIORAL).
Who is sponsoring clinical trial NCT06892275?
This trial is sponsored by Georgetown University, which has 227 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06892275 being conducted?
This trial has 1 study location across District of Columbia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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