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Clinical Trials/NCT00857103
NCT00857103
Completed
N/A

Improving Patient-Provider Communication in Cancer Care

Oslo University Hospital1 site in 1 country200 target enrollmentAugust 2006
ConditionsLymphoma

Overview

Phase
N/A
Intervention
Not specified
Conditions
Lymphoma
Sponsor
Oslo University Hospital
Enrollment
200
Locations
1
Primary Endpoint
Patient satisfaction
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

This interdisciplinary international research collaboration will test effects of Choice, a computer-assisted, interactive support system designed to help cancer patients communicate their symptoms and preferences, and clinicians in incorporating this information into patient care. In this pretest-post test clinical trial with 200 leukemia and lymphoma patients we will: 1) Test effects of Choice when integrated into routine clinical practice on: patient-provider communication, documented patient care, anxiety and patient satisfaction; 2) analyze relationships among the above variables and explore differences in these relationships between groups; 3) analyze group differences in communication style in terms of instrumental and affective behavior, content, participation, initiative and person addressed; and 4) investigate the extent of the time requirements when using Choice in clinical practice, perceived usefulness and ease of use.

Detailed Description

Improving shared decision making (SDM), patient-provider communication and incorporating patients' illness experiences and preferences into patient care are high priority health policy goals. However, this is difficult to accomplish without methods and systems that assist patients in sharing their illness experiences and clinicians in integrating this information into patient care. Choice is a computer-assisted, interactive communication and support system for cancer patients designed for this purpose. This interdisciplinary, international research collaboration will test effects of Choice in a pretest-post test clinical trial with 200 leukemia and lymphoma patients. We hypothesize that when patients use Choice for symptom and preference assessments and this information is provided to their clinicians to support consultations in routine practice, (1) patient-provider communication will be more patient-centered; (2) documented care will be more congruent with patients' reported symptoms and preferences; (3) patients will experience lower levels of anxiety and stress during consultations; and (4) they will be more satisfied with the consultation than the "usual care" control group. To better understand the mechanisms by which these effects occur, we will investigate relationships between communication style, documented patient care, anxiety and satisfaction; and explore time requirements, perceived usefulness and ease of use of Choice by patients and clinicians. Controlling for gender, age, diagnosis and type/stage of treatment, analyses of covariance and repeated measurement models will be primarily used for hypotheses testing, correlations and descriptive statistics to answer research questions. This study will contribute to new technologies to support SDM and patient-provider partnerships in health care that can significantly improve patient-provider communication, patient-centered care and physical, emotional and psycho-social well-being of cancer patients.

Registry
clinicaltrials.gov
Start Date
August 2006
End Date
June 2009
Last Updated
12 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Oslo University Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Diagnosed with leukemia or lymphoma and in treatment or follow up after treatment within last 12 months.
  • Being able to understand, speak and write Norwegian.
  • Informed consent

Exclusion Criteria

  • If clinician know patient will receive bad news regarding outcome.

Outcomes

Primary Outcomes

Patient satisfaction

Time Frame: one point assessment

Anxiety

Time Frame: one point assessment

communication

Time Frame: one point assessment

Study Sites (1)

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