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Educational Intervention for Breast Cancer Risk

N/A
Waitlist Available
Led By Kent Hoskins, M.D.
Research Sponsored by University of Illinois at Chicago
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
No prior history of breast cancer
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 months
Awards & highlights

Study Summary

This trial will test whether an educational intervention can help patients understand their cancer risk.

Who is the study for?
This trial is for African American women aged 25-69 who are recommended for genetic counseling based on a cancer risk assessment done during their mammogram at UI Health. They must not have had breast cancer before or previous genetic counseling for hereditary breast cancer risk, and they should be able to consent and complete surveys in English.Check my eligibility
What is being tested?
The study is testing the effectiveness of an educational video intervention used alongside a genetic risk assessment during mammography appointments to see if it increases the uptake of genetic counseling among participants.See study design
What are the potential side effects?
Since this trial involves an educational video as an intervention, there are no direct medical side effects associated with it. However, participants may experience emotional or psychological responses to learning about their breast cancer risks.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I have never had breast cancer before.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 3 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Knowledge and intentions regarding genetic counseling
Secondary outcome measures
Attendance at genetic counseling appointment

Trial Design

1Treatment groups
Experimental Treatment
Group I: Open LabelExperimental Treatment1 Intervention
Educational genetic counseling video
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Educational video
2014
Completed Phase 3
~3610

Find a Location

Who is running the clinical trial?

University of Illinois at ChicagoLead Sponsor
607 Previous Clinical Trials
1,558,396 Total Patients Enrolled
Kent Hoskins, M.D.Principal InvestigatorUniversity of Illinois at Chicago
1 Previous Clinical Trials
13 Total Patients Enrolled

Media Library

Open Label Clinical Trial Eligibility Overview. Trial Name: NCT04082117 — N/A
Breast Cancer Risk Research Study Groups: Open Label
Breast Cancer Risk Clinical Trial 2023: Open Label Highlights & Side Effects. Trial Name: NCT04082117 — N/A
Open Label 2023 Treatment Timeline for Medical Study. Trial Name: NCT04082117 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is this experiment open to adults aged sixty and above?

"To meet the requirements of this clinical trial, patients must be between 25 and 69 years old. Elsewhere on the site there are 64 studies recruiting participants below 18 years in age, as well as 2209 trials for people above 65."

Answered by AI

What qualifications must individuals possess to be accepted into this research program?

"The enrollment conditions for this medical trial mandate that participants must have a breast cancer diagnosis and be between 25 to 69 years old. The study is seeking 960 people in total."

Answered by AI

Are researchers presently recruiting for this investigation?

"According to clinicaltrials.gov, the study in question is no longer recruiting patients at this time; the first posting was on May 12th 2017 and its last update was June 22nd 2022. However, there are still 2,291 other trials actively enrolling participants as of now."

Answered by AI
~0 spots leftby May 2024