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Clinical Trials/NCT01972048
NCT01972048WithdrawnNot Applicable

Mobile Phone Multimedia Messaging Intervention for Breast Cancer Screening: Intervention Phase

University of Minnesota1 site in 1 countryStarted: January 1, 2014Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Withdrawn
Locations
1
Primary Endpoint
Mammogram receipt

Study Overview

Brief 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.

Detailed 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.

Study Design

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

Eligibility Criteria

Ages
40 Years to 79 Years (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

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

Arms & Interventions

Control group

Active Comparator

Participants in the control group will receive the mailed print brochure about breast cancer screening and community resources.

Intervention: Print brochure (Other)

Intervention group

Experimental

Participants will receive the mMammogram intervention.

Intervention: mMammogram (Behavioral)

Outcomes

Primary Outcomes

Mammogram receipt

Time Frame: 1 week

The receipt of mammogram (or scheduled appointment) will be measured by self-report.

Secondary Outcomes

  • Breast cancer knowledge(1 week)
  • Breast cancer health beliefs(1 week)
  • Participant intent to undergo screening(1 week)
  • Culture specific attitudes toward breast cancer(1 week)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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