Measuring Quality of Life in Routine Oncology Practice Improves Communication and Patient Well-Being: A Randomized Controlled Trial
Top Cited Papers
- 15 February 2004
- journal article
- clinical trial
- Published by American Society of Clinical Oncology (ASCO) in Journal of Clinical Oncology
- Vol. 22 (4) , 714-724
- https://doi.org/10.1200/jco.2004.06.078
Abstract
Purpose: To examine the effects on process of care and patient well-being, of the regular collection and use of health-related quality-of-life (HRQL) data in oncology practice. Patients and Methods: In a prospective study with repeated measures involving 28 oncologists, 286 cancer patients were randomly assigned to either the intervention group (regular completion of European Organization for Research and Treatment of Cancer-Core Quality of Life Questionnaire version 3.0, and Hospital Anxiety and Depression Scale on touch-screen computers in clinic and feedback of results to physicians); attention-control group (completion of questionnaires, but no feedback); or control group (no HRQL measurement in clinic before encounters). Primary outcomes were patient HRQL over time, measured by the Functional Assessment of Cancer Therapy-General questionnaire, physician-patient communication, and clinical management, measured by content analysis of tape-recorded encounters. Analysis employed mixed-effects modeling and multiple regression. Results: Patients in the intervention and attention-control groups had better HRQL than the control group (P = .006 and P = .01, respectively), but the intervention and attention-control groups were not significantly different (P = .80). A positive effect on emotional well-being was associated with feedback of data (P = .008), but not with instrument completion (P = .12). A larger proportion of intervention patients showed clinically meaningful improvement in HRQL. More frequent discussion of chronic nonspecific symptoms (P = .03) was found in the intervention group, without prolonging encounters. There was no detectable effect on patient management (P = .60). In the intervention patients, HRQL improvement was associated with explicit use of HRQL data (P = .016), discussion of pain, and role function (P = .046). Conclusion: Routine assessment of cancer patients' HRQL had an impact on physician-patient communication and resulted in benefits for some patients, who had better HRQL and emotional functioning.Keywords
This publication has 26 references indexed in Scilit:
- Computer-based quality of life questionnaires may contribute to doctor–patient interactions in oncologyBritish Journal of Cancer, 2002
- Psychiatric morbidity and its recognition by doctors in patients with cancerBritish Journal of Cancer, 2001
- Oncologists' recognition of depression in their patients with cancer.Journal of Clinical Oncology, 1998
- Cancer's Psychological ChallengesScientific American, 1996
- The routine use of health-related quality of life measures in the care of patients with epilepsy: rationale and research agendaQuality of Life Research, 1995
- Quality of life and the patient with cancer. Individual and policy implicationsCancer, 1994
- Recent Developments and Future Issues in the Use of Health Status Assessment Measures in Clinical SettingsMedical Care, 1992
- Case-Mix Groups for VA Hospital-Based Home CareMedical Care, 1992
- Improving Patient Function: A Randomized Trial of Functional Disability ScreeningAnnals of Internal Medicine, 1989
- The Need for a New Medical Model: A Challenge for BiomedicineScience, 1977