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临床试验/NCT06739733
NCT06739733进行中(未招募)不适用

Effectiveness of Soft Robotic Glove Versus EMS on Hand Function and Quality of Life in Stroke Survivors. A Randomized Clinical Trial

Superior University1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2024年3月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
36
试验地点
1
主要终点
The Fugl-Meyer Upper Extremity Assessment (FMA-UE)

研究概览

简要总结

This study will evaluate the effectiveness of soft robotic gloves versus electrical muscle stimulation (EMS) in improving hand function and quality of life in stroke survivors. Stroke often leads to impaired hand mobility, impacting daily activities and reducing overall quality of life. Soft robotic gloves, designed to assist with hand movement, will provide mechanical support and encourage voluntary muscle activity. EMS, on the other hand, will stimulate muscle contraction through electrical impulses, potentially enhancing muscle strength and coordination.

详细描述

Participants will be divided into two groups: one will receive treatment using soft robotic gloves, and the other with EMS. Outcomes will be assessed using standardized hand function tests and quality-of-life questionnaires over a specified period. Results are expected to indicate that both interventions will improve hand function and quality of life, with the robotic gloves showing a marginally greater improvement in dexterity and grip strength, while EMS will yield benefits in muscle reactivation and endurance. Stroke survivors in the robotic glove group are anticipated to report greater ease in performing daily tasks, while the EMS group will note an increase in muscle engagement.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
50 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Had ischemic or hemorrhagic stroke ≤6 months.
  • Mini-mental status exam scores > 24(7).
  • GCS score 11 to 15(2)
  • FMA-UE score < 21(3)

排除标准

  • Participants with severe vision or hearing impairment.
  • Neurological disorders including epilepsy, Alzheimer's disease, vertigo, Parkinson disease, and , muscular disorders which limit functional activity (OA, RA, etc).
  • Peripheral vestibular disorder.
  • Medications that affect balance, severe cardiovascular conditions, recent lower limb injury or surgery.
  • Contraindications for EMS: Patients with certain medical conditions, such as pacemakers, implantable cardioverter-defibrillators, or metal fragments in their body, that contraindicated the use of EMS were excluded.

结局指标

主要结局

The Fugl-Meyer Upper Extremity Assessment (FMA-UE)

时间窗: 12 Months

The Fugl-Meyer Upper Extremity Assessment (FMA-UE) is a standardized tool used to evaluate motor function, sensation, coordination, and joint motion in individuals with upper limb impairments, often post-stroke. It is based on a hierarchical framework of motor recovery, covering movements from basic reflexes to voluntary motor control. The assessment includes various sections focusing on shoulder, elbow, forearm, wrist, hand, and coordination. Each item measures specific movement tasks, allowing therapists to track progress over time. The FMA-UE is widely used in clinical settings for its reliability and validity in evaluating upper extremity function. Scoring The FMA-UE has 33 items, each scored on a 3-point scale: 0 = Cannot perform 1. = Partially performs 2. = Fully performs The total score ranges from 0 to 66 points (higher scores indicate better motor function).

The Quick Disabilities of the Arm, Shoulder, and Hand (QuickDASH)

时间窗: 12 months

The Quick Disabilities of the Arm, Shoulder, and Hand (QuickDASH) is a shortened version of the DASH outcome measure used to assess physical function and symptoms in individuals with upper extremity conditions. It consists of 11 questions evaluating difficulty in performing daily activities, severity of symptoms (pain, tingling, weakness), and social and emotional impacts. The QuickDASH is designed for fast administration and is applicable across various musculoskeletal disorders. It provides insight into functional limitations, helping guide treatment planning. Scoring Each item is rated on a 1-5 Likert scale (1 = no difficulty, 5 = extreme difficulty). Scores are averaged, transformed into a scale of 0 to 100 (0 = no disability, 100 = most severe disability). An optional Work and Sports/Performing Arts module adds context-specific insights.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Muhammad Naveed Babur

Principal Investigator

Superior University

研究点 (1)

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