一种提高脑卒中后康复剂量的技术强化方法:临床可行性研究。

IF 2.6 3区 医学 Q1 REHABILITATION
Clinical Rehabilitation Pub Date : 2025-06-01 Epub Date: 2025-04-18 DOI:10.1177/02692155251333542
Gillian Sweeney, Fiona Boyd, Maisie Keogh, Patrycja Lyczba, Elaine Forrest, Philip Rowe, Mark Barber, Andy Kerr
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引用次数: 0

摘要

目的探讨一种多技术、以群体为基础的脑卒中后早期增加康复剂量方法的可行性。方法采用混合方法设计招募、退出、安全性、剂量和可接受性报告。急性住院卒中单位研究对象60例卒中患者,卒中后中位数9.0 (IQR 12.8)天,转介康复治疗,无轻度运动禁忌症。干预:除常规护理外,在有监督的小组中使用多技术康复健身房进行个性化康复。可行性基于每月3.2以上的招募率,低于6%的辍学率,没有疑似意外严重不良反应和低于60%的肩部疼痛患病率。可接受性来源于与临床团队的访谈。手工记录剂量(康复时间)。用改良的Rivermead活动指数和治疗结果测量法测量功能。结果可行性令人满意,招募率高(6人/月),退出率低(2%),无疑似意外严重不良反应,肩痛发生率低(19%)。访谈数据的专题分析表明,临床团队(n = 9)认为干预是可以接受的,并确定了组织对更高剂量的限制。参与者在住院期间(23.0天,SD 19.7)平均参加9.1次(1-32次)疗程,疗程平均持续52分钟(SD 15.7)。改良后的Rivermead活动指数和治疗结果测量分别提高了17.9点(SD 8.6)和5.7点(SD 2.4)。结论强有力的可行性研究结果支持未来多技术、基于群体的康复试验。这种新方法是实现中风后康复推荐剂量的令人鼓舞的一步,但需要进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A technology-enriched approach to increasing rehabilitation dose after stroke: Clinical feasibility study.

ObjectiveTo assess the feasibility of a multi-technology, group based, approach to increasing rehabilitation dose early after stroke.MethodsMixed methods design reporting recruitment, dropout, safety, dose and acceptability.SettingAcute Hospital Stroke UnitParticipantsSixty stroke patients, 9.0 median (IQR 12.8) days after stroke, referred for rehabilitation, without contraindications to light exercise.InterventionPersonalised rehabilitation delivered in supervised groups, using a multi-technology rehabilitation gym, in addition to usual care.Main measuresFeasibility was based on achieving recruitment rates over 3.2 per month, dropout rates below 6%, absence of suspected unexpected serious adverse reactions and shoulder pain prevalence below 60%. Acceptability was derived from interviews with the clinical team. Dose (rehabilitation time) was recorded manually. Function was measured with the modified Rivermead Mobility Index and Therapy Outcome Measure.ResultsFeasibility was satisfactory with high recruitment rates (6 per month), low dropout (2%), no suspected unexpected serious adverse reactions and low prevalence (19%) of shoulder pain. Thematic analysis of interview data indicated the clinical team (n = 9) found the intervention acceptable and identified organisational constraints to higher doses. Participants attended an average of 9.1 (1-32) sessions during their hospital stay (23.0 days, SD 19.7), with sessions lasting 52 min (SD 15.7), on average. The modified Rivermead Mobility Index and Therapy Outcome Measure increased by 17.9 (SD 8.6) and 5.7 points (SD 2.4), respectively.ConclusionsStrong feasibility findings support future trials of multi-technology, group-based rehabilitation. This novel approach is an encouraging step toward achieving recommended doses of rehabilitation after stroke but needs further investigation.

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来源期刊
Clinical Rehabilitation
Clinical Rehabilitation 医学-康复医学
CiteScore
5.60
自引率
6.70%
发文量
117
审稿时长
4-8 weeks
期刊介绍: Clinical Rehabilitation covering the whole field of disability and rehabilitation, this peer-reviewed journal publishes research and discussion articles and acts as a forum for the international dissemination and exchange of information amongst the large number of professionals involved in rehabilitation. This journal is a member of the Committee on Publication Ethics (COPE)
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