NCT01972048

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.

Trial Health

30
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Timeline
Completed

Started Jan 2014

Geographic Reach
1 country

1 active site

Status
withdrawn

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 24, 2013

Completed
6 days until next milestone

First Posted

Study publicly available on registry

October 30, 2013

Completed
2 months until next milestone

Study Start

First participant enrolled

January 1, 2014

Completed
2.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2016

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2016

Completed
Last Updated

January 26, 2018

Status Verified

January 1, 2018

Enrollment Period

2.2 years

First QC Date

October 24, 2013

Last Update Submit

January 24, 2018

Conditions

Keywords

breast cancerbreast cancer screeningmammogram

Outcome Measures

Primary Outcomes (1)

  • Mammogram receipt

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

    1 week

Secondary Outcomes (4)

  • Breast cancer knowledge

    1 week

  • Breast cancer health beliefs

    1 week

  • Culture specific attitudes toward breast cancer

    1 week

  • Participant intent to undergo screening

    1 week

Study Arms (2)

Control group

ACTIVE COMPARATOR

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

Other: Print brochure

Intervention group

EXPERIMENTAL

Participants will receive the mMammogram intervention.

Behavioral: mMammogram

Interventions

mMammogramBEHAVIORAL

Text messages delivered via mobile app to participants designed to inform them about breast cancer screening and encourage them to schedule a mammogram.

Intervention group

Mailed print brochure about breast cancer screening and community resources.

Control group

Eligibility Criteria

Age40 Years - 79 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

  • Mammogram receipt within the past 2 years

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Minnesota Masonic Cancer Center

Minneapolis, Minnesota, 55455, United States

Location

Related Publications (1)

  • Lee H, Ghebre R, Le C, Jang YJ, Sharratt M, Yee D. Mobile Phone Multilevel and Multimedia Messaging Intervention for Breast Cancer Screening: Pilot Randomized Controlled Trial. JMIR Mhealth Uhealth. 2017 Nov 7;5(11):e154. doi: 10.2196/mhealth.7091.

MeSH Terms

Conditions

Breast Neoplasms

Condition Hierarchy (Ancestors)

Neoplasms by SiteNeoplasmsBreast DiseasesSkin DiseasesSkin and Connective Tissue Diseases

Study Officials

  • Hee Y Lee, PhD

    University of Minnesota

    PRINCIPAL INVESTIGATOR
0

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 24, 2013

First Posted

October 30, 2013

Study Start

January 1, 2014

Primary Completion

March 1, 2016

Study Completion

May 1, 2016

Last Updated

January 26, 2018

Record last verified: 2018-01

Locations