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Engaging Diverse Underserved Communities to Bridge the Mammography Divide


N/A
40 Years
N/A
Open (Enrolling)
Female
Breast Cancer Screening

Thank you

Trial Information

Engaging Diverse Underserved Communities to Bridge the Mammography Divide


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.


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

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Screening

Outcome Measure:

120-day post randomization mammography screening completion

Outcome Description:

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).

Outcome Time Frame:

day 120

Safety Issue:

No

Principal Investigator

Kimberly Engelman, PhD

Investigator Role:

Principal Investigator

Investigator Affiliation:

University of Kansas

Authority:

United States: Institutional Review Board

Study ID:

12371

NCT ID:

NCT01267110

Start Date:

September 2010

Completion Date:

June 2015

Related Keywords:

  • Breast Cancer Screening
  • Breast Neoplasms

Name

Location

University of Kansas Medical Center Kansas City, Kansas  66160-7353