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Effects of a Self-Monitoring Quality of Life Intervention for Patients with Cancer Receiving Palliative Care in Japan: Study Protocol for a Randomized Controlled Trial
Authors:Ayako Matsuda1Yosuke Yamada2Noriko Ishizuka3Eisuke Matsushima3Kunihiko Kobayashi4Takayoshi Ohkubo1Kazue Yamaoka5
Affiliation:1Teikyo University School of Medicine, Department of Hygiene and Public Health, Tokyo, Japan.2Toshima Hospital, Division Chief of Palliative Care Unit, Tokyo, Japan.3Tokyo Medical and Dental University, Graduate School of Medical and Dental Sciences, Section of Liaison Psychiatry and Palliative Medicine, Tokyo, Japan.4Saitama Medical University International Medical Center, Department of General Thoracic Surgery, Saitama, Japan.5Teikyo University Graduate School of Public Health, Tokyo, Japan.
Abstract:Background: Previous studies suggest the use of patient-reported outcome measures in routine clinical practice hasimportant benefits for patients with cancer, particularly as feedback regarding patients’ quality of life (QOL) improvesdoctor-patient communication and clinical decision making. This study aimed to examine the effect of using the CareNotebook as a routine self-monitoring QOL intervention in clinical practice for patients with cancer receiving palliativecare. The results are expected to clarify the practical use of the Care Notebook in this population. Methods: Thisprospective randomized study is being undertaken at Toshima Hospital, Japan. Participating patients who are randomlyassigned to the intervention group will be asked to complete the shortened Care Notebook booklet for patients withcancer in palliative care once each day. A control group will receive usual care. The primary outcome is global healthstatus/QOL (Global QOL), as assessed by the European Organization for Research and Treatment of Cancer Quality ofLife Questionnaire Core 15 Palliative. Data will be collected at baseline (after allocation), and at 1 week and 3 weeksin both the control and intervention groups. The effects of the intervention will be evaluated with a mixed randomeffects model. The required sample size is 200 patients. We obtained approval from Toshima Hospital (No 26-11) andthe Tokyo Medical and Dental University Ethics Committee (No 1756). The findings will be disseminated throughpublications in peer-reviewed journals and attendance at domestic and international conferences. The trial was registeredwith the UMIN clinical trials registry (Trial registration number: UMIN000025322). Conclusions: This study willprovide evidence on whether medical staff can use the Care Notebook as a routine self-monitoring QOL intervention inclinical practice for patients with cancer receiving palliative care. We expect that a routine Care Notebook interventionfor patients with cancer will be recommended in healthcare facilities.
Keywords:Self monitoring  Quality of Life  cancer  palliative care
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