Computer Program in Improving Communication Between Doctors and Patients With Stage IV Cancer

Duke University

Status: Completed

Conditions: Unspecified Adult Solid Tumor, Protocol Specific

Treatments: Behavioral: communication lecture; Behavioral: lecture plus CD-ROM

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT00276627

CDR0000452788 (Other Identifier)

Pro00010216

DUMC-4510-05-2RER

Details and patient eligibility

About

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.

Full 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.

Enrollment: 800 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS:

• Diagnosis of advanced cancer (stage IV disease) AND meets all of the following criteria:

  • Referred by participating physician
  • Must speak English
  • Receiving primary oncology care at participating centers, defined as at least 2 visits to the clinic during the past year and a future scheduled appointment
  • Receiving treatment for any malignancy
  • Has access to a telephone

PATIENT CHARACTERISTICS:

• Not specified

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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800 participants in 2 patient groups

communication lecture

Active Comparator group

Treatment:

Behavioral: communication lecture

lecture plus CD-ROM

Experimental group

Treatment:

Behavioral: lecture plus CD-ROM