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Clinical Trials/NCT01267110
NCT01267110CompletedNot Applicable

Engaging Diverse Underserved Communities to Bridge the Mammography Divide

University of Kansas1 site in 1 country261 target enrollmentStarted: September 1, 2010Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
261
Locations
1
Primary Endpoint
120-day post randomization mammography screening completion

Study Overview

Brief Summary

Breast cancer is the second most common cause of cancer death in the U.S.1 in spite of being preventable, easily detectable, and curable.2-11 Breast screening continues to be underutilized by the general population and especially by traditionally underserved minority populations. Two of the least screened minority groups are American Indians/Alaska Natives (AI/AN) and Latinas. American Indian/Alaska Native women have the poorest recorded 5-year cancer survival rates of any ethnic group and the lowest (or near-lowest) screening rates for major cancers.12 Furthermore, breast cancer is the number one cause of cancer mortality among Latina women.13 While breast cancer screening rates have increased nationally, there has been an increase in the gap in breast cancer screening utilization between individuals from minority versus majority racial/ethnic groups.

Detailed Description

If you decide to participate in the program, your participation will last 4 months. You will complete the Healthy Living Kansas-Breast Health survey by computer. The survey will take about 20 minutes to complete. You will be randomly assigned (like flipping a coin) to one of two groups. The groups will receive different breast health information. After completing the survey, you agree to be contacted by telephone in 4 months to answer questions. You will be asked for your name, home address, and phone number.

You will be given information about breast cancer and mammography. You may or may not benefit from the information provided. Care will be taken to safeguard the information you provide but under rare circumstances confidentiality breaches may occur.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Screening
Masking
None

Eligibility Criteria

Ages
40 Years to — (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Latina or AI/AN woman residing in one of participating communities
  • •Aged ≥40 years of age
  • •Not up to date on mammography screening
  • •Home address & access to a working telephone
  • •Responded to 120-day post randomization follow-up call

Exclusion Criteria

  • •Receipt of mammogram within past year
  • •Acute medical illness, history of breast cancer, 1st
  • •Cognitive impairment or inappropriate affect or behavior
  • •Another household member enrolled in the study

Arms & Interventions

Intervention

Experimental

Intervention: MI2 intervention arm (Other)

Control

Active Comparator

Intervention: Control (Other)

Outcomes

Primary Outcomes

120-day post randomization mammography screening completion

Time Frame: day 120

To compare the 120-day post randomization mammography screening completion rates of individuals who receive a computerized mammography "implementation intentions" (MI2) intervention, versus a comparison computerized condition of general breast cancer prevention health education (C).

Secondary Outcomes

  • To compare changes in mammography screening Precaution Adoption Process Model(day 120)
  • To compare the screening mammography self-reported barriers after 120-days post randomization(day 120)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Kimberly Engelman, PhD

Associate Professor

University of Kansas

Study Sites (1)

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