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Clinical Trials/NCT02296177
NCT02296177
Completed
Not Applicable

Evidence Based Dissemination for Mammography Adherence in Safety Net Communities

The University of Texas Health Science Center, Houston1 site in 1 country4,448 target enrollmentJuly 2015
ConditionsBreast Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Breast Cancer
Sponsor
The University of Texas Health Science Center, Houston
Enrollment
4448
Locations
1
Primary Endpoint
Mammography Appointment Adherence
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Breast cancer is the most common cancer and the second leading cause of cancer related death in American women. Regular screening, early diagnosis, and timely treatment initiation have been shown to reduce breast cancer morbidity and mortality. However, disparities continue to exist across the breast cancer continuum for underserved women, particularly minority women. The reduction of disparities in breast cancer outcomes is a major goal of Healthy People 2020 and the National Cancer Institute. However, the preventable burden of late stage breast cancer will continue until the investigators close the gap between what is known about prevention and what is implemented in the community. Although many sources of information exist about theory and [theory-] and evidence-based interventions (EBIs) to promote mammography screening, their adoption and use in the community has been limited and haphazard at best.

Detailed Description

In order to effectively reach underserved women and reduce breast cancer disparities, D\&I efforts should target the healthcare delivery system where these women receive service - the so called "safety net". Within the safety net, federally qualified health centers (FQHCs), provide comprehensive primary health care services for underserved communities regardless of ability to pay, including mammography screening. Our team has successfully pilot tested a National Cancer Institute research tested intervention program (RTIP) with underserved women and were able to reduce no-show rates from 44% to 19%. In order to accelerate the adoption and implementation of our EBI within the safety net, the investigators will use a two-step approach based on the consolidated framework for implementation research (CFIR), and intervention mapping. The investigators will actively disseminate the EBI through a unique breast health collaborative with a wide membership of FQHCs, support implementation through training and evaluate the adoption, implementation, sustainment and effectiveness of the EBI. The investigators will use a clinic clustered stepped wedge design for implementation in FQHCs.

Registry
clinicaltrials.gov
Start Date
July 2015
End Date
March 2018
Last Updated
2 years ago
Study Type
Interventional
Study Design
Crossover
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Linda Highfield

Assistant Professor

The University of Texas Health Science Center, Houston

Eligibility Criteria

Inclusion Criteria

  • Underserved as defined by income \<=200% of the federal poverty level for a family of four
  • Uninsured
  • In need of mammography screening; has received clinical breast exam and referral to screening
  • Has upcoming screening appointment

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Mammography Appointment Adherence

Time Frame: 12 months

Appointment attendance will be taken from the electronic health record for both control and intervention patients

Secondary Outcomes

  • Cancellations or rescheduled appointments(12 months)

Study Sites (1)

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