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研究方案:GOAL 试验:对患有慢性肾脏病的体弱老年人进行全面老年评估以增加患者确定目标的实现-一项整群随机对照试验。

Study protocol for The GOAL Trial: comprehensive geriatric assessment for frail older people with chronic kidney disease to increase attainment of patient-identified goals-a cluster randomised controlled trial.

机构信息

Centre for Health Services Research, University of Queensland, Brisbane, Australia.

Australasian Kidney Trials Network, University of Queensland, Brisbane, Australia.

出版信息

Trials. 2023 May 30;24(1):365. doi: 10.1186/s13063-023-07363-4.

Abstract

BACKGROUND

An increasing number of older people are living with chronic kidney disease (CKD). Many have complex healthcare needs and are at risk of deteriorating health and functional status, which can adversely affect their quality of life. Comprehensive geriatric assessment (CGA) is an effective intervention to improve survival and independence of older people, but its clinical utility and cost-effectiveness in frail older people living with CKD is unknown.

METHODS

The GOAL Trial is a pragmatic, multi-centre, open-label, superiority, cluster randomised controlled trial developed by consumers, clinicians, and researchers. It has a two-arm design, CGA compared with standard care, with 1:1 allocation of a total of 16 clusters. Within each cluster, study participants ≥ 65 years of age (or ≥ 55 years if Aboriginal or Torres Strait Islander (First Nations Australians)) with CKD stage 3-5/5D who are frail, measured by a Frailty Index (FI) of > 0.25, are recruited. Participants in intervention clusters receive a CGA by a geriatrician to identify medical, social, and functional needs, optimise medication prescribing, and arrange multidisciplinary referral if required. Those in standard care clusters receive usual care. The primary outcome is attainment of self-identified goals assessed by standardised Goal Attainment Scaling (GAS) at 3 months. Secondary outcomes include GAS at 6 and 12 months, quality of life (EQ-5D-5L), frailty (Frailty Index - Short Form), transfer to residential aged care facilities, cost-effectiveness, and safety (cause-specific hospitalisations, mortality). A process evaluation will be conducted in parallel with the trial including whether the intervention was delivered as intended, any issue or local barriers to intervention delivery, and perceptions of the intervention by participants. The trial has 90% power to detect a clinically meaningful mean difference in GAS of 10 units.

DISCUSSION

This trial addresses patient-prioritised outcomes. It will be conducted, disseminated and implemented by clinicians and researchers in partnership with consumers. If CGA is found to have clinical and cost-effectiveness for frail older people with CKD, the intervention framework could be embedded into routine clinical practice. The implementation of the trial's findings will be supported by presentations at conferences and forums with clinicians and consumers at specifically convened workshops, to enable rapid adoption into practice and policy for both nephrology and geriatric disciplines. It has potential to materially advance patient-centred care and improve clinical and patient-reported outcomes (including quality of life) for frail older people living with CKD.

TRIAL REGISTRATION

ClinicalTrials.gov NCT04538157. Registered on 3 September 2020.

摘要

背景

越来越多的老年人患有慢性肾脏病(CKD)。许多人有复杂的医疗保健需求,并且存在健康和功能状况恶化的风险,这会对他们的生活质量产生不利影响。综合老年评估(CGA)是一种有效的干预措施,可以提高老年人的生存率和独立性,但在患有 CKD 的脆弱老年人中,其临床实用性和成本效益尚不清楚。

方法

GOAL 试验是一项由消费者、临床医生和研究人员共同制定的实用、多中心、开放标签、优效性、集群随机对照试验。它采用两臂设计,CGA 与标准护理相比,共有 16 个集群的分配比例为 1:1。在每个集群中,招募年龄≥65 岁(或如果是原住民或托雷斯海峡岛民(第一民族澳大利亚人)则≥55 岁)的患有 CKD 3-5/5D 期且虚弱的患者,其虚弱程度通过衰弱指数(FI)>0.25 来衡量。干预集群中的参与者接受老年病学家的 CGA,以确定医疗、社会和功能需求,优化药物处方,并在需要时安排多学科转诊。标准护理集群中的参与者接受常规护理。主要结局是通过标准化目标实现量表(GAS)在 3 个月时评估自我确定的目标。次要结局包括 6 个月和 12 个月时的 GAS、生活质量(EQ-5D-5L)、虚弱(简短形式的衰弱指数)、转移到养老院、成本效益和安全性(特定原因的住院、死亡率)。将同时进行一项过程评估,包括干预是否按计划实施、干预实施过程中的任何问题或当地障碍以及参与者对干预的看法。该试验有 90%的把握检测出 GAS 平均差异 10 个单位的临床有意义差异。

讨论

该试验解决了患者优先的结果。它将由临床医生和研究人员与消费者合作进行、传播和实施。如果 CGA 对患有 CKD 的脆弱老年人具有临床和成本效益,那么干预框架可以嵌入到常规临床实践中。试验结果的实施将通过会议演示和与临床医生和消费者在专门召开的研讨会上进行的讨论来支持,以实现肾脏病学和老年医学学科的快速采用。它有可能极大地推进以患者为中心的护理,并改善患有 CKD 的脆弱老年人的临床和患者报告的结果(包括生活质量)。

试验注册

ClinicalTrials.gov NCT04538157。2020 年 9 月 3 日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8450/10230758/6a476f047771/13063_2023_7363_Fig1_HTML.jpg

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