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Clinical Trials/NCT00276627
NCT00276627
Completed
Not Applicable

Enhancing Patient-Oncologist Communication

Duke University2 sites in 1 country800 target enrollmentFebruary 2003

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Unspecified Adult Solid Tumor, Protocol Specific
Sponsor
Duke University
Enrollment
800
Locations
2
Primary Endpoint
Number of empathic statements and responses to patients' expressions of negative emotion
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

RATIONALE: A computer program and education materials may help improve the ability of doctors to communicate with patients.

PURPOSE: This randomized clinical trial is studying how well a computer program together with education materials works in improving communication between doctors and patients with stage IV cancer.

Detailed Description

OBJECTIVES: Primary * Determine the impact of a CD-ROM-based intervention in improving communication behaviors between oncologists and patients with stage IV cancer. * Compare the quality of audio-recorded conversations between oncologists and patients with advanced cancer with best practices described in the literature, with particular attention to communication behaviors that promote patient disclosure of concerns, use of emotion handling skills, recognition of empathic opportunities, and the conveying of prognostic information and compare. * Develop an intervention to improve oncologists' communication skills in these areas using an interactive CD-ROM based on the oncologists' own recorded discussions with patients. * Determine the feasibility of this intervention and, using a randomized, controlled design, measure its effectiveness for changing physician communication behaviors and relevant patient outcomes including reduced distress and increased satisfaction. OUTLINE: This is a randomized, controlled, 3-part, multicenter study. * Part 1 (baseline): Patients undergo an audio-recorded outpatient encounter with their oncologist to see how oncologists elicit patients' concerns and respond to emotional content. Within 1 week later, patients undergo a 10-minute interview by telephone. * Part 2 (intervention): Oncologists are randomized to 1 of 2 arms. * Arm I (intervention): Oncologists receive a personalized, user-friendly CD-ROM that contains their coded conversations, packaged with related educational material to be used for 3 months. * Arm II (control): Oncologists do not receive a CD-ROM or any other educational material support. * Part 3 (post-intervention): Three months later, oncologists in both arms are reassessed by recording another 400 clinic visits between the same oncologists and a new group of patients to measure the intervention impact. PROJECTED ACCRUAL: A total of 800 patients will be accrued for this study.

Registry
clinicaltrials.gov
Start Date
February 2003
End Date
February 2006
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Number of empathic statements and responses to patients' expressions of negative emotion

Time Frame: Postintervention audio recordings and follow-up surveys

Postintervention audio recordings were used to identify the number of empathic statements and responses to patients' expressions of negative emotion. Surveys evaluated patients' trust in their oncologists and perceptions of their oncologists' communication skills.

Study Sites (2)

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