Study protocol for a randomized controlled trial: Integrating the 'Time-limited Trial' in the emergency department.

IF 2.6 3区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
PLoS ONE Pub Date : 2024-12-23 eCollection Date: 2024-01-01 DOI:10.1371/journal.pone.0313858
Tadayuki Hashimoto, Rachel K Putman, Anthony F Massaro, Youkie Shiozawa, Katherine McGough, Kerry K McCabe, Judith A Linden, Wei Wang, Shan W Liu, Maura Kennedy, Thanh H Neville, Jacqueline M Kruser, Rebecca L Sudore, Mara A Schonberg, James A Tulsky, Kei Ouchi
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引用次数: 0

Abstract

Introduction: Time-limited trial (TLT) is a structured approach between clinicians and seriously ill patients or their surrogates to discuss patients' values and preferences, prognosis, and shared decision-making to use specific therapies for a prespecified period of time in the face of prognostic uncertainty. Some evidence exists that this approach may lead to more patient-centered care in the intensive care unit; however, it has never been evaluated in the emergency department (ED). The study protocol aims to assess the feasibility and acceptability of TLTs initiated in the ED.

Methods and analysis: We will conduct a parallel group, clinician-level, pilot randomized clinical trial among 40 ED clinicians. We will measure feasibility (e.g., the time it takes to conduct the TLTs by ED clinicians) and clinician and patient-reported acceptability of the TLT, and also track patients' clinical outcomes via medical record review.

Discussion: This study protocol will investigate the potential of TLT initiated in the ED to lead to patient-centered intensive care utilization. By doing so, the study intends to improve palliative care integration for seriously ill older adults in the ED and intensive care unit.

Trial identifier and registry name: ClinicalTrials.gov ID: NCT06378151 https://clinicaltrials.gov/study/NCT06378151; Pre-results; a randomized controlled trial: Time-limited Trials in the Emergency Department.

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随机对照试验的研究方案:将“限时试验”纳入急诊科。
简介:时间限制试验(TLT)是临床医生和重症患者或其代理人之间讨论患者的价值观和偏好、预后,并在面对预后不确定性时共同决策在预先指定的时间内使用特定治疗的结构化方法。一些证据表明,这种方法可能会导致重症监护室更多的以患者为中心的护理;然而,它从未在急诊科(ED)进行评估。研究方案旨在评估在急诊科开展tlt的可行性和可接受性。方法和分析:我们将在40名急诊科临床医生中进行平行组、临床水平、试点随机临床试验。我们将衡量可行性(例如,ED临床医生进行TLT所需的时间)以及临床医生和患者报告的TLT可接受性,并通过医疗记录审查跟踪患者的临床结果。讨论:本研究方案将探讨在急诊科开展TLT以实现以患者为中心的重症监护利用的潜力。通过这样做,本研究旨在改善重症老年人在急诊科和重症监护病房的姑息治疗整合。试验标识符和注册中心名称:ClinicalTrials.gov ID: NCT06378151 https://clinicaltrials.gov/study/NCT06378151;Pre-results;随机对照试验:急诊科的限时试验
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来源期刊
PLoS ONE
PLoS ONE 生物-生物学
CiteScore
6.20
自引率
5.40%
发文量
14242
审稿时长
3.7 months
期刊介绍: PLOS ONE is an international, peer-reviewed, open-access, online publication. PLOS ONE welcomes reports on primary research from any scientific discipline. It provides: * Open-access—freely accessible online, authors retain copyright * Fast publication times * Peer review by expert, practicing researchers * Post-publication tools to indicate quality and impact * Community-based dialogue on articles * Worldwide media coverage
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