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Breast Cancer Screening Via Computer V. Phone

Breast Cancer Screening Via Computer V. Phone

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00287040
Enrollment
1686
Registered
2006-02-06
Start date
2007-09-30
Completion date
2009-06-30
Last updated
2012-05-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer Screening

Keywords

Breast Cancer, Mammography

Brief 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.

Detailed 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.

Interventions

BEHAVIORALTailored, interactive intervention for mammography screening

Follow ups will occur at 6-, 12-, and 21-months in order to determine effectiveness of intervention as well as cost effectiveness and variation based on participant characteristics to facilitate a more effective program for mammography screenings

Sponsors

National Institute of Nursing Research (NINR)
CollaboratorNIH
National Cancer Institute (NCI)
CollaboratorNIH
Indiana University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
41 Years to 75 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
To increase annual mammography adherenceat 6-, 12-, and 21-Months

Secondary

MeasureTime frame
Cost-effectiveness of DVD versus telephone surveyat 6-, 12-, and 21-months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026