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Mobile Phone Multimedia Messaging Intervention for Breast Cancer Screening

University of Minnesota (UMN) logo

University of Minnesota (UMN)

Status

Withdrawn

Conditions

Breast Cancer

Treatments

Other: Print brochure
Behavioral: mMammogram

Study type

Interventional

Funder types

Other

Identifiers

NCT01972048
2013NTLS063

Details and patient eligibility

About

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.

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.

Sex

Female

Ages

40 to 79 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

0 participants in 2 patient groups

Control group
Active Comparator group
Description:
Participants in the control group will receive the mailed print brochure about breast cancer screening and community resources.
Treatment:
Other: Print brochure
Intervention group
Experimental group
Description:
Participants will receive the mMammogram intervention.
Treatment:
Behavioral: mMammogram

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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