Status:

COMPLETED

Intervention Study of Communication in Oncologist-Patient Encounters

Lead Sponsor:

Duke University

Collaborating Sponsors:

National Cancer Institute (NCI)

Conditions:

Advanced Cancer

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

The overall goal of this study is to improve communication between patients with advanced cancer and their oncologists. A web-based communication intervention will be delivered to patients to help the...

Detailed Description

Patients will be recruited from the practices of participating oncologists; therefore, physicians will be enrolled prior to their patients. All medical, surgical and radiation oncology faculty and hem...

Eligibility Criteria

Inclusion

  • speak English;
  • have a diagnosis of advanced cancer (Stage IV or however defined for that disease group), metastatic disease, or refractory or recurrent illness;
  • have access to a telephone; and,
  • have regular access to a computer with broadband Internet service and an email account.

Exclusion

  • incompetent for interview (documented diagnosis of active psychosis or dementia) or unable to provide informed consent as assessed by the interviewer;
  • hearing impaired or have a speech disorder;
  • physically impaired in such a way that precludes the use of a computer;
  • simply too sick to participate, and cannot realistically participate in the interview, as judged by the research assistant; or
  • does not have another appointment with an enrolled oncologist within three months.
  • has dial-up Internet service, or
  • does not meet IES Score.
  • While only patient subjects with advanced cancer will be eligible for randomization into one of the study arms, healthy volunteers (providers and third parties) will be enrolled in the study, too. Patients will be recruited from the practices of participating oncologists; therefore, physicians will be enrolled prior to their patients. All medical, surgical and radiation oncology faculty and hematology/oncology fellows who see patients in the participating clinics will be eligible for the study. We also will enroll the mid-level providers (i.e., physician assistants and nurse practitioners) who work with many of these oncologists and any third party (friends, family members) who comes to clinic with the enrolled patient.

Key Trial Info

Start Date :

November 1 2010

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

April 1 2014

Estimated Enrollment :

659 Patients enrolled

Trial Details

Trial ID

NCT00994578

Start Date

November 1 2010

End Date

April 1 2014

Last Update

September 12 2014

Active Locations (2)

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Page 1 of 1 (2 locations)

1

Duke University Health System

Durham, North Carolina, United States, 27705

2

University of Pittsburgh Medical Center

Pittsburgh, Pennsylvania, United States, 15213-2582