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NCT03511690 · ClinicalTrials.gov registry record · NA

Testing an Intelligent Tutoring System to Enhance Genetic Risk Assessment

A NA study of Hereditary Breast and Ovarian Cancer, sponsored by Georgetown University.

Completed
Registry status
NA
Development phase
95
Enrollment target
4
Study locations

NCT03511690 is a NA study of Hereditary Breast and Ovarian Cancer that has completed, run by Georgetown University. The registered enrollment target is 95 participants, below the 587-participant average among 5 other Hereditary Breast and Ovarian Cancer trials with a reported enrollment target (84% lower). The trial reports 4 study locations across 2 states.

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The verdict

NCT03511690, a NA study of Hereditary Breast and Ovarian Cancer, has completed, sponsored by Georgetown University.

COMPLETED
Registry status
NA
Development phase
95 participants
Enrollment target
4
Study locations

Study Summary

Participating in genetic cancer risk assessments (GCRA) for hereditary breast and ovarian cancer can inform treatment and risk management decisions and improve breast cancer outcomes. However, Latina and Black women underuse GCRA services, which may increase breast cancer disparities. This study will adapt and test the impact of an easily scalable novel Tutoring System intervention to enhance GCRA use and improve psychosocial outcomes in a clinical sample of underserved Latina and Black women at risk of hereditary breast and ovarian cancer.

Interventions

  • BEHAVIORAL BRCA-Gist

Study Locations (4)

District of Columbia

  • Capital Breast Care Center - Washington D.C.
  • Georgetown University - Washington D.C.

Virginia

  • Nueva Vida - Alexandria
  • Virginia Commonwealth University - Richmond

Trial Details

FieldValue
Enrollment Target 95 participants
Start Date 2017-07-01
Est. Completion 2022-02-20
Phase NA

Sponsor

Georgetown University

227 total trials

What the Registry Record Tells You About NCT03511690

The ClinicalTrials.gov registry entry for NCT03511690 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 95 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 587-participant average among 5 other Hereditary Breast and Ovarian Cancer trials with a reported enrollment target (84% lower). The listed sponsor is Georgetown University, which has 227 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Hereditary Breast and Ovarian Cancer appearing as the primary indexed condition, and to 1 intervention - of which BRCA-Gist is the first listed.

NCT03511690 reports 4 study locations spanning 2 distinct geographic areas - top geographies include District of Columbia, Virginia.

Frequently Asked Questions

What is clinical trial NCT03511690 about?

NCT03511690 is a clinical study titled "Testing an Intelligent Tutoring System to Enhance Genetic Risk Assessment". Participating in genetic cancer risk assessments (GCRA) for hereditary breast and ovarian cancer can inform treatment and risk management decisions and improve breast cancer outcomes. However, Latina and Black women underuse GCRA services, which may increase breast cancer disparities. This study wil...

What is the current status of trial NCT03511690?

This trial is currently completed. It is a NA study. The enrollment target is 95 participants. The study started on 2017-07-01. Estimated completion is 2022-02-20.

What conditions does trial NCT03511690 study?

This clinical trial studies the following conditions: Hereditary Breast and Ovarian Cancer.

What interventions are being tested in trial NCT03511690?

The interventions under investigation include: BRCA-Gist (BEHAVIORAL).

Who is sponsoring clinical trial NCT03511690?

This trial is sponsored by Georgetown University, which has 227 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03511690 being conducted?

This trial has 4 study locations across District of Columbia, Virginia. 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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