Breast Cancer Clinical Trial

Mobile Phone Multimedia Messaging Intervention for Breast Cancer Screening

Summary

Korean American (KA) women have among the highest breast cancer mortality rates and lowest breast cancer screening rates of U.S. American women across racial/ethical groups. This innovative project seeks to harness mobile phone technology as a means to take preventative health care to a new level among this population. Using the Fogg Behavioral Model this study proposes to develop a mobile phone-based intervention designed to motivate KA women to undergo an annual mammogram (mMammogram). The overall study aim is to develop and assess the feasibility and effectiveness of a 7-day long mMammogram intervention designed to persuade KA women to undergo breast cancer screening.

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Full Description

Specific aims over the three-year period include the following: (1) The first year will be devoted to intervention and protocol development. A major emphasis in year 1 will be developing the community advisory board (CAB), conducting a series of pre-intervention focus groups, and working with pertinent persuasive technology consultants to develop and pilot-test the intervention. (2) The second year and the first half of the third year will focus on delivery of the intervention. (3) the second half of the third year will be devoted to data analysis and dissemination.

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Eligibility Criteria

Inclusion Criteria:

Korean American immigrant women
Aged 40-79
Residence in Minnesota
Possession of mobile phone with text-message function
Possession of active email account

Exclusion Criteria:

Mammogram receipt within the past 2 years

Study is for people with:

Breast Cancer

Study ID:

NCT01972048

Recruitment Status:

Withdrawn

Sponsor:

University of Minnesota

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There is 1 Location for this study

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University of Minnesota Masonic Cancer Center
Minneapolis Minnesota, 55455, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Study ID:

NCT01972048

Recruitment Status:

Withdrawn

Sponsor:


University of Minnesota

How clear is this clinincal trial information?

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