CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 100 enrolled
Drug / intervention
Patient Preference in Treatment Decision Makingbehavioral
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03350854
NCT03350854N/ACompleted

An Intervention to Improve Decision Role Concordance Amongst Newly Diagnosed Breast Cancer Patients

University of Utah·interventional·Posted Nov 22, 2017·Updated Nov 22, 2017

In Brief

A clinical study evaluating Patient Preference in Treatment Decision Making for Breast Cancer. Completed, enrolled 100 participants.

Detailed Summary

The goal of this project is to test the effects of the Patient Preference Scale as the basis for a clinical intervention for role negotiation in breast cancer surgery decisions and the Patient Perception Scale to measure role concordance. The investigators hypothesize that better role concordance will be achieved with a simple provider-based intervention. In the first half of the study, providers will be blind to the patient's preferred role. In the second half, providers will be made aware of the preferred role prior to the encounter and will have a brief conversation with the patient about their desired role in the decision making process.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsBreast Cancer
Countries--
Collaborators--

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedNov 22, 2017
Enrollment StartMar 7, 2016
Primary CompletionJan 31, 2017
Study CompletionAug 9, 2017
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 8.6 years ago

Interventions

Patient Preference in Treatment Decision Makingbehavioral

The roles are divided into two active roles, a collaborative (or shared) role, and two passive roles in the Patient Preference scale questionnaire. Once the questionnaire is administered, the patient will then proceed to original surgical appointment. The provider is informed of the patient's preferred role and has a discussion with them patient about this in the intervention group, but not in the control group.