Kim Grace J, Gahlot Amanda, Magsombol Camile, Waskiewicz Margaret, Capasso Nettie, Van Lew Stephen, Kim Hayejin, Parnandi Avinash, Dickson Victoria Vaughan, Goverover Yael
Department of Occupational Therapy, NYU Steinhardt School of Culture, Education, and Human Development, New York, NY.
Department of Occupational Therapy, NYU Langone Health, Rusk Rehabilitation, New York, NY.
Arch Rehabil Res Clin Transl. 2024 Jan 18;6(1):100316. doi: 10.1016/j.arrct.2023.100316. eCollection 2024 Mar.
To determine the feasibility of a self-directed training protocol to promote actual arm use in everyday life. The secondary aim was to explore the initial efficacy on upper extremity (UE) outcome measures.
Feasibility study using multiple methods.
Home and outpatient research lab.
Fifteen adults (6 women, 9 men, mean age=53.08 years) with chronic stroke living in the community. There was wide range of UE functional levels, ranging from dependent stabilizer (limited function) to functional assist (high function).
Use My Arm-Remote protocol. Phase 1 consisted of clinician training on motivational interviewing (MI). Phase 2 consisted of MI sessions with participants to determine participant generated goals, training activities, and training schedules. Phase 3 consisted of UE task-oriented training (60 minutes/day, 5 days/week, for 4 weeks). Participants received daily surveys through an app to monitor arm training behavior and weekly virtual check-ins with clinicians to problem-solve challenges and adjust treatment plans.
Primary outcome measures were feasibility domains after intervention, measured by quantitative study data and qualitative semi-structured interviews. Secondary outcomes included the Canadian Occupational Performance Measure (COPM), Motor Activity Log (MAL), Fugl-Meyer Assessment (FMA), and accelerometry-based duration of use metric measured at baseline, discharge, and 4-week follow-up.
The UMA-R was feasible in the following domains: recruitment rate, retention rate, intervention acceptance, intervention delivery, adherence frequency, and safety. Adherence to duration of daily practice did not meet our criteria. Improvements in UE outcomes were achieved at discharge and maintained at follow-up as measured by COPM-Performance subscale (F[1.42, 19.83]=17.72, <.001) and COPM-Satisfaction subscale (F[2, 28]=14.73, <.001), MAL (F[1.31, 18.30]=12.05, <.01) and the FMA (F[2, 28]=16.62, <.001).
The UMA-R was feasible and safe to implement for individuals living in the community with chronic stroke. Adherence duration was identified as area of refinement. Participants demonstrated improvements in standardized UE outcomes to support initial efficacy of the UMA-R. Shared decision-making and behavior change frameworks can support the implementation of UE self-directed rehabilitation. Our results warrant the refinement and further testing of the UMA-R.
确定一种自我指导训练方案在促进日常生活中实际使用手臂的可行性。次要目的是探讨该方案对上肢(UE)结局指标的初始疗效。
采用多种方法的可行性研究。
家庭和门诊研究实验室。
15名居住在社区的慢性卒中成年患者(6名女性,9名男性,平均年龄 = 53.08岁)。UE功能水平范围广泛,从依赖稳定型(功能受限)到功能辅助型(功能良好)。
采用My Arm-Remote方案。第1阶段包括临床医生进行动机性访谈(MI)培训。第2阶段包括与参与者进行MI环节,以确定参与者制定的目标、训练活动和训练计划。第3阶段包括以UE任务为导向的训练(每天60分钟,每周5天,共4周)。参与者通过应用程序接受每日调查,以监测手臂训练行为,并每周与临床医生进行虚拟签到,以解决挑战并调整治疗计划。
主要结局指标是干预后的可行性领域,通过定量研究数据和定性半结构化访谈进行测量。次要结局包括加拿大职业表现测量量表(COPM)、运动活动日志(MAL)、Fugl-Meyer评估量表(FMA),以及在基线、出院时和4周随访时基于加速度计测量的使用时长指标。
UMA-R在以下领域是可行的:招募率、保留率、干预接受度、干预实施、依从频率和安全性。每日练习时长的依从性未达到我们的标准。通过COPM-表现子量表(F[1.42, 19.83]=17.72, <.001)、COPM-满意度子量表(F[2, 28]=14.73, <.001)、MAL(F[1.31, 18.30]=12.05, <.01)和FMA(F[2, 28]=16.62, <.001)测量,出院时UE结局得到改善,并在随访时保持。
对于居住在社区的慢性卒中患者,UMA-R的实施是可行且安全的。确定了依从时长是需要改进的方面。参与者在标准化UE结局方面表现出改善,以支持UMA-R的初始疗效。共同决策和行为改变框架可支持UE自我指导康复的实施。我们的结果值得对UMA-R进行改进和进一步测试。