出院后电话随访对患者家庭护理的影响:随机对照试验的研究方案

Tsukasa Domoto, Y. Matsumura, Midori Fukada
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引用次数: 0

摘要

目的:通过医院护士对护理经理的定期电话随访,了解患者出院后的困难情况。方法:采用随机对照试验和前瞻性随机、开放盲法终点评价来检验干预的效果。这项研究的目标是65岁以上的病人,需要一个护理经理,离开医院到他们的家或住宅护理机构。参与者,50对患者和护理经理,将为本研究提供同意。在干预组,从医院护士到护理经理的电话随访将进行三次:出院后一周、一个月和两个月;对照组将遵循标准方案。出院后困难自理问卷调查2次(出院后1周和2个月),组间比较结果。并对干预组10名护理管理者进行访谈,对访谈内容进行分析,作为过程评价。讨论:本研究的新颖之处在于通过电话随访加强了工作人员之间的合作,并对患者的不安和沮丧进行了评估。如果有效,电话随访可以系统化并纳入标准治疗。此外,适当的时间,时间和电话随访的频率可能会随着研究而变得清晰。在未来的研究中,根据本研究的结果制定新的随访方案,并对其效果进行检验,将有助于随访体系的发展。试验注册:本研究于2018年5月7日在UMIN临床试验注册中心注册(ID: UMIN000032251)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects on Patients Home Care by Telephone Follow-up after Hospital Discharge: Study Protocol of a Randomized Controlled Trial
Objective: To investigate patients’ post-discharge difficulties through periodic telephone follow-ups from the hospital nurse to the care manager.Methods: The effects of the intervention will be examined using a randomized controlled trial and prospective randomized, open blinded-endpoint evaluation. This research targets patients who are older than 65 years of age, require a care manager and leave the hospital for their homes or residential care facilities. The participants, 50 pairs of patients and care managers, will provide consent for this study. In the intervention group, telephone follow ups from the hospital nurse to the care manager will be carried out three times: one week, one month, and two months after discharge; the control group will follow standard protocols. A self-administered questionnaire survey about difficulties after discharge will be conducted twice (one week and two months after discharge), and the results will be compared between groups. In addition, 10 care managers from the intervention group will be interviewed, and the contents will be analyzed as a process evaluation.Discussion: The novelty of this study is that it strengthens the cooperation between the staff using telephone follow-ups and the evaluates the patients’ unease and frustration. If effective, the telephone follow-up could be systematized and incorporated into standard care. Furthermore, the appropriate period, timing, and frequency of telephone follow-ups may become clear with the study. In terms of future research, the development of a new follow up program based on the results of this study and the examination of its effects will contribute to the development of the follow-up system.Trial registration: This study was registered with the UMIN Clinical Trials Registry on May 7, 2018 (ID: UMIN000032251).
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