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SupporTive Care At Home Research (STAHR) for patients with advanced cancer: Protocol for a cluster non-randomized controlled trialopen access

Authors
Lee, Dong-WookLee, Sun YoungYoo, Shin HyeKim, Kyae HyungKim, Min-SunShin, JeongmiHwang, In-YoungHwang, In GyuBaek, Sun KyungKim, Do YeunKim, Yu JungKang, BeodeulLee, JoongyubCho, Belong
Issue Date
May-2024
Publisher
Public Library of Science
Citation
PloS one, v.19, no.5
Journal Title
PloS one
Volume
19
Number
5
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/73953
DOI
10.1371/journal.pone.0302011
ISSN
1932-6203
1932-6203
Abstract
Advancements in the treatment and management of patients with cancer have extended their survival period. To honor such patients' desire to live in their own homes, home-based supportive care programs have become an important medical practice. This study aims to investigate the effects of a multidimensional and integrated home-based supportive care program on patients with advanced cancer. SupporTive Care At Home Research is a cluster non-randomized controlled trial for patients with advanced cancer. This study tests the effects of the home-based supportive care program we developed versus standard oncology care. The home-based supportive care program is based on a specialized home-based medical team approach that includes (1) initial assessment and education for patients and their family caregivers, (2) home visits by nurses, (3) biweekly regular check-ups/evaluation and management, (4) telephone communication via a daytime access line, and (5) monthly multidisciplinary team meetings. The primary outcome measure is unplanned hospitalization within 6 months following enrollment. Healthcare service use; quality of life; pain and symptom control; emotional status; satisfaction with services; end-of-life care; advance planning; family caregivers' quality of life, care burden, and preparedness for caregiving; and medical expenses will be surveyed. We plan to recruit a total of 396 patients with advanced cancer from six institutions. Patients recruited from three institutions will constitute the intervention group, whereas those recruited from the other three institutions will comprise the control group. Copyright: © 2024 Lee et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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의과대학 (의학부(임상-서울))
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