呼吸力量训练与呼吸放松训练在脑卒中后肢体损伤、功能康复和重新参与中的应用:随机对照试验方案》。

IF 1.4 Q3 HEALTH CARE SCIENCES & SERVICES
Dorian K Rose, Gina Brunetti, Kathryn Cavka, J Brooke Hoisington, Hannah Snyder, Wei Xue, Barbara K Smith
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引用次数: 0

摘要

背景:慢性中风幸存者的持续残疾通常归因于手臂或腿部无力;然而,呼吸肌无力也会阻碍中风后的康复、降低生活质量并增加健康并发症的风险。呼吸系统并发症在中风后很常见,使患者面临长期功能障碍和死亡的风险。此外,中风幸存者还面临着持续的心血管疾病,使他们面临中风复发的风险:本研究旨在比较两种呼吸训练计划以及个性化的柔韧性、强化和心血管锻炼计划对慢性中风幸存者的生理、活动和社会参与结果的影响:本研究将是一项随机对照试验。方法:本研究将采用随机对照试验的方式,参与者为 80 名居住在社区的慢性中风成年患者。参加者将被随机分配接受呼吸力量训练或呼吸放松训练,与此同时,参加者还将接受美国心脏协会提供的为期 24 节(每周 3 次,共 8 周)的全身锻炼计划。研究干预将由理疗师指导,在社区健身中心进行。结果评估将在临床研究中心进行。主要结果指标是最大呼吸压力。次要结果指标包括气道通畅度、行走耐力、空间-时间步态特征、社区行走、功能强度和疲劳、抑郁以及社会参与度。长期社会参与是一个复杂的领域,可能受到身体功能以外的其他因素的影响。在干预后的 1 年中,将对参与者的健康状况进行监测,包括跌倒、呼吸系统疾病和住院情况。其他子分析将评估烟雾暴露对短期和长期结果的影响。结果评估人员对组别分配实行盲法。呼吸放松训练是一项积极的比较研究,但不包括纯对照组:这项研究于 2020 年 3 月获得资助,并于 2020 年 11 月开始招生。预计 2025 年 5 月完成注册,2026 年 4 月研究结束。预计 2026 年秋季公布结果:这项研究的结果将使我们更好地了解呼吸锻炼对这些人的短期和长期生理、功能和社会收益的额外益处。这些数据将有助于满足目前尚未满足的康复需求,促进以患者为中心的护理,并有助于降低慢性中风幸存者的发病率和死亡率:试验注册:ClinicalTrials.gov:试验注册:ClinicalTrials.gov:NCT05819333;https://clinicaltrials.gov/study/NCT05819333.International 注册报告标识符(irrid):DERR1-10.2196/59749。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Respiratory Strength Training Versus Respiratory Relaxation Training in the Rehabilitation of Physical Impairment, Function, and Return to Participation After Stroke: Protocol for a Randomized Controlled Trial.

Background: Persistent disability in chronic stroke survivors is often attributed to arm or leg weakness; however, respiratory muscle weakness also impedes poststroke rehabilitation, reduces quality of life, and increases the risk of health complications. Respiratory complications are common after stroke and place patients at risk for both prolonged functional disability and mortality. In addition, stroke survivors face ongoing cardiovascular disease that places them at risk for recurrent stroke.

Objective: The study aims to compare the effects of 2 respiratory training programs, paired with individualized flexibility, strengthening, and cardiovascular exercise programs, on physiologic, activity, and societal participation outcomes in chronic stroke survivors.

Methods: This study will be a randomized controlled trial. Participants are 80 community-dwelling adults with chronic stroke. In conjunction with a 24-session (3 times/week for 8 weeks), American Heart Association-informed, whole-body exercise program, participants will be randomized to receive either respiratory strength training or respiratory relaxation training. Study intervention will be directed by a physical therapist and take place in a community fitness center. Outcome assessments will occur in a clinical research center. The primary outcome measure is maximal respiratory pressure. Secondary outcome measures include airway clearance, walking endurance, spatial-temporal gait characteristics, community walking, functional strength and fatigue, depression, and societal participation measures. Longer-term societal participation is a complex domain that may be influenced by other factors beyond physical function. Participants' health status will be monitored for 1 year following the intervention for falls, respiratory illness, and hospitalizations. Additional subanalyses will evaluate the effect of smoke exposure on short- and long-term outcomes. Outcome assessors are blinded to group assignments. Respiratory relaxation training is an active comparator, but no pure control group is included.

Results: This study was funded in March 2020 with enrollment commencing in November 2020. Completion of enrollment is projected for May 2025 with a study projected end date of April 2026. Published results are anticipated in Fall 2026.

Conclusions: Results from this study will improve our understanding of the additive benefits of respiratory exercises on short- and long-term physiologic, functional, and societal gains for these individuals. These data will be instructive to meet a current unmet rehabilitative need to promote patient-centered care and contribute to decreasing morbidity and mortality in chronic stroke survivors.

Trial registration: ClinicalTrials.gov: NCT05819333; https://clinicaltrials.gov/study/NCT05819333.

International registered report identifier (irrid): DERR1-10.2196/59749.

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来源期刊
CiteScore
2.40
自引率
5.90%
发文量
414
审稿时长
12 weeks
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