Breast Cancer Clinical Trial

Breast Cancer Screening Via Computer V. Phone

Summary

The purpose of this study is to compare mammography adherence among women receiving tailored, interactive mammography interventions via DVD and telephone counseling to usual care.

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Full Description

Efficacy Study - We will use stratified block randomization based on race to ensure that the treatment groups maintain comparable race composition. Participants will be randomly assigned to one of the intervention groups or to usual care. Intervention Group 1 will receive, by mail, a DVD version of the interactive computer program; based on responses to its queries, the program will supply immediate feedback to promote mammography. Intervention Group 2 will receive a telephone version of the tailored intervention delivered by a counselor stationed at a computer. The counselor will use questions from the interactive program and deliver messages the program generates in response to each woman's answers. A third group will receive usual care. All women will be asked to participate in 6-month and 21-month follow-up telephone interviews querying stage of mammography adherence and beliefs.

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Eligibility Criteria

Inclusion Criteria:

• Must have been a member of their HMO/insurance plan for at least 15 months with records indicating no mammogram (screening or diagnostic) in that 15-month period

Current member of the plan at time of study enrollment
No history of breast cancer diagnosis
Complete telephone number and mailing address

Exclusion Criteria:

• Any claim submitted for a mammogram (screening or diagnostic) in the last 15 months within the HMO/insurance plan or an outside source

Previous breast cancer diagnosis
Incomplete telephone number or mailing address

Study is for people with:

Breast Cancer

Phase:

Phase 3

Estimated Enrollment:

1686

Study ID:

NCT00287040

Recruitment Status:

Completed

Sponsor:

Indiana University

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There is 1 Location for this study

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Indiana University
Indianapolis Indiana, 46202, United States
Duke University
Durham North Carolina, , United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 3

Estimated Enrollment:

1686

Study ID:

NCT00287040

Recruitment Status:

Completed

Sponsor:


Indiana University

How clear is this clinincal trial information?

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