COMPLETED

Developing and Evaluating Culturally Relevant Interventions to Improve Breast Cancer Screening

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this study is to evaluate the relative benefits of an intervention to promote breast cancer screening among women in the White Mountain Apache (WMA) community. Women will be randomized to receive CARE, a culturally tailored mammography education module, or CARE+COACH, which is the CARE education module plus access to an Apache paraprofessional women's health coach (i.e., patient navigator). The CARE intervention was developed through a community-based participatory research process. The primary outcome is mammography uptake within 2 months of a referral.

Official Title

Developing and Evaluating Scalable and Culturally Relevant Interventions to Improve Breast Cancer Screening Among White Mountain Apache Women

Quick Facts

Study Start:2023-06-06
Study Completion:2025-10-20
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT05665660

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:Not specified
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Referral for screening mammography from a Whiteriver Indian Health Service provider
  2. * Self-identify as American Indian or Alaska Native (AIAN)
  3. * Female
  4. * Live on within 60 miles of the Fort Apache Indian Reservation
  1. * Women who have received a mammogram within the prior 12 months
  2. * Women with a personal history of breast cancer
  3. * Unable to participate in full intervention or evaluation due to an anticipated event (e.g., planned move)
  4. * Unwilling to be randomized

Contacts and Locations

Principal Investigator

Allison Barlow, PhD
PRINCIPAL_INVESTIGATOR
Johns Hopkins Bloomberg School of Public Health

Study Locations (Sites)

Center for Indigenous Health
Whiteriver, Arizona, 85941
United States

Collaborators and Investigators

Sponsor: Johns Hopkins Bloomberg School of Public Health

  • Allison Barlow, PhD, PRINCIPAL_INVESTIGATOR, Johns Hopkins Bloomberg School of Public Health

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-06-06
Study Completion Date2025-10-20

Study Record Updates

Study Start Date2023-06-06
Study Completion Date2025-10-20

Terms related to this study

Keywords Provided by Researchers

  • mammography
  • cancer screening

Additional Relevant MeSH Terms

  • Breast Cancer