A Randomized Controlled Trial Evaluating the Impact of Pre-Operative Web-based Breast Cancer Information on the Quality of Patient Decision-Making

University of Wisconsin, Madison0 sites244 target enrollmentApril 24, 2014

ConditionsBreast Cancer Knowledge, Attitudes, Practice

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: Breast Cancer
Sponsor: University of Wisconsin, Madison
Enrollment: 244
Primary Endpoint: Knowledge using the Breast Cancer Decision Quality Instrument
Status: Completed
Last Updated: 2 years ago

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

This is a prospective randomized control trial to compare the impact of two different types of pre-operative web-based breast cancer information on the quality of patient decision making. Patients are emailed web-based information prior to the surgical consultation. Outcomes are assess at multiple time points: 1) prior to the surgical consultation, 2) immediately following the consultation.

Registry

clinicaltrials.gov

Start Date

April 24, 2014

End Date

June 28, 2016

Last Updated

2 years ago

Study Type

Interventional

Study Design

Parallel

Sex

Female

Investigators

Sponsor

University of Wisconsin, Madison

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Outcomes

Primary Outcomes

Knowledge using the Breast Cancer Decision Quality Instrument

Time Frame: immediately prior to the surgical consultation

Secondary Outcomes

Perceived communication with the breast surgeon using the Breast Cancer Decision Quality Instrument(following the surgical consultation but prior to the surgery)
Decisional concordance using the Breast Cancer Decision Quality Instrument(immediately prior to the surgical consultation)
Breast surgeon and staff (nurse, mid-level provider) assessment of how the web-based decision aid versus standard high-quality breast cancer websites influenced their patient interactions, based on Practitioner Opinion Survey(at completion of patient accrual, estimated to be 2 years after initiating study)