2019
DOI: 10.6004/jnccn.2018.7106
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Advance Care Planning Improves Psychological Symptoms But Not Quality of Life and Preferred End-of-Life Care of Patients With Cancer

Abstract: Background: This study was conducted to examine whether a longitudinal advance care planning (ACP) intervention facilitates concordance between the preferred and received life-sustaining treatments (LSTs) of terminally ill patients with cancer and improves quality of life (QoL), anxiety symptoms, and depressive symptoms during the dying process. Patients and Methods: Of 795 terminally ill patients with cancer from a medical center in Taiwan, 460 were recruited and randomly assigned 1:1 to the experimental and … Show more

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Cited by 35 publications
(71 citation statements)
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“…Video‐only interventions varied in length from 3 to 20 minutes, 94,95 and some included accompanying questions 96 . Some depicted medical situations, such as simulated resuscitation, 94 health trajectories of long‐term care residents, 97 and specific dementia, heart failure, and other serious illness content 64,98‐100 …”
Section: Resultsmentioning
confidence: 99%
“…Video‐only interventions varied in length from 3 to 20 minutes, 94,95 and some included accompanying questions 96 . Some depicted medical situations, such as simulated resuscitation, 94 health trajectories of long‐term care residents, 97 and specific dementia, heart failure, and other serious illness content 64,98‐100 …”
Section: Resultsmentioning
confidence: 99%
“…Between-arm baseline characteristics, accurate PA, DNR order issued, and LST preferences were balanced at randomization. 37 Data collectors were blinded to arm assignment. No research staff were involved in clinical care.…”
Section: Overview and Samplementioning
confidence: 99%
“…Detailed information has been reported previously about the study design, sample size calculation, participant recruitment, treatments for each arm, treatment fidelity assurance, and assessments. 37 The RCT study protocol (supplemental eAppendix 1) was approved by the ethics committee of the study site and registered at ClinicalTrials.gov (ClinicalTrials.gov identifier: NCT01912846). All participants provided written informed consent before enrollment.…”
Section: Overview and Samplementioning
confidence: 99%
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