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BRCA-Gist for Breast and Ovarian Cancer

N/A
Waitlist Available
Led By Alejandra H Hurtado de Mendoza, PhD
Research Sponsored by Georgetown University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up within one hour before the intervention and within one hour post-intervention
Awards & highlights
No Placebo-Only Group

Summary

This trial will test an intervention to improve cancer outcomes in Latina and Black women by increasing their participation in genetic cancer risk assessments.

Eligible Conditions
  • Breast and Ovarian Cancer

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~within one hour before the intervention and within one hour post-intervention
This trial's timeline: 3 weeks for screening, Varies for treatment, and within one hour before the intervention and within one hour post-intervention for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Breast Cancer Genetics Knowledge
Intentions to participate in genetic counseling
Perceived pros and cons of genetic counseling and testing
Secondary study objectives
Declarative Knowledge of Breast Cancer, Genetic Testing, and Genetic Risk
Emotions about developing breast cancer and about participating in genetic counseling
Malignant Neoplasms
+4 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Group I: Immediate BRCA-Gist InterventionExperimental Treatment1 Intervention
Participants randomized to immediate BRCA-gist will complete the adapted intervention and immediately complete a baseline survey. They will be asked to complete a second survey two weeks after completion of the first one. BRCA-gist is a web-based tutoring system that emulates one-to-one human tutoring via avatars to communicate risk of BRCA1/2. We estimate a completion time of 90 minutes.
Group II: Delayed BRCA-Gist InterventionExperimental Treatment1 Intervention
Participants randomized to delayed BRCA-gist will initially complete a baseline survey. Two weeks after completion of that survey, they will complete the adapted intervention and immediately complete a second survey.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
BRCA-Gist
2017
N/A
~100

Find a Location

Who is running the clinical trial?

Georgetown UniversityLead Sponsor
350 Previous Clinical Trials
139,069 Total Patients Enrolled
Virginia Commonwealth UniversityOTHER
716 Previous Clinical Trials
22,888,403 Total Patients Enrolled
Cornell UniversityOTHER
171 Previous Clinical Trials
14,088,687 Total Patients Enrolled
~11 spots leftby Dec 2025