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Overcoming Racial Disparities in Screening Mammography

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The Washington University

Status

Begins enrollment this month

Conditions

Breast Cancer
Cancer of the Breast

Treatments

Other: Automated phone call
Other: Digital navigation video
Other: Telephone counseling
Other: Appointment mail reminder

Study type

Interventional

Funder types

Other
NETWORK
Industry

Identifiers

NCT07549139
202604048

Details and patient eligibility

About

The purpose of this study is to increase screening mammography among Black women by implementing and evaluating a culturally tailored patient-centric program designed to address barriers to screening. By performing a randomized clinical trial, this study aims to develop effective strategies to improve adherence to screening mammography and contribute to reducing health disparities in breast cancer outcomes.

Enrollment

176 estimated patients

Sex

Female

Ages

40+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Woman
  • At least 40 years old
  • Self-identify as Black
  • English-speaking
  • Scheduled for a screening mammogram within 8 weeks of study entry
  • Able to understand and willing to sign an IRB approved written informed consent document.

Exclusion criteria

  • A previous history of breast cancer
  • Scheduled for a diagnostic mammogram
  • Has a documented or uncorrectable cognitive, hearing, or visual impairment.
  • Too ill to participate (diagnosed with or suffering from a condition that, in the judgment of the investigator, may limit participation in the study).

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

176 participants in 2 patient groups

Arm 1: Usual Care
Active Comparator group
Description:
Patients will receive the institution's usual care for screening mammogram, which consists of an automated reminder phone call from the breast health center 1-3 days prior to a scheduled appointment.
Treatment:
Other: Automated phone call
Arm 2: Culturally Tailored Patient Centric Program Methods
Experimental group
Description:
Patients will receive mail reminders at 7-10 days prior to appointment, tailored telephone counseling to both serve as an appointment reminder and to identify and troubleshoot salient barriers to mammography completion, and a digital navigation video explaining the rationale for and the actual mammography procedure. All study procedures are carried out remotely with no additional research visits for participants.
Treatment:
Other: Appointment mail reminder
Other: Telephone counseling
Other: Digital navigation video

Trial contacts and locations

1

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Central trial contact

Foluso Ademuyiwa, MD, MPH, MSCI

Data sourced from clinicaltrials.gov

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