部分冈上肌撕裂的VR辅助康复治疗
虚拟现实辅助康复对部分冈上肌撕裂患者疼痛、运动恐惧、生活质量和冈上肌腱厚度影响的随机对照试验
背景:
基于虚拟现实(VR)的康复治疗最近已成为一种有前景的方法,旨在增强患者参与度并改善肌肉骨骼疾病的康复效果。然而,关于其在部分冈上肌腱撕裂患者中有效性的证据仍然有限。
目的:
这项随机对照研究旨在探讨VR辅助康复对部分冈上肌腱撕裂患者的疼痛、功能障碍、运动恐惧症、生活质量和冈上肌腱厚度的影响。
方法:
本研究纳入了49名年龄在18-65岁之间的部分冈上肌腱撕裂患者。所有参与者在三周内接受了15次治疗,包括热敷、治疗性超声波和经皮电神经刺激。虚拟现实(VR)组进行了基于VR的交互式锻炼,而对照组则进行传统治疗性锻炼。干预前后评估了疼痛强度(数字评分量表)、肩关节活动范围、功能状态(肩痛与功能障碍指数)、运动恐惧症(坦帕运动恐惧症量表)、生活质量(SF-36)以及通过超声检查评估的冈上肌腱厚度。
研究概览
地位
详细说明
肩痛是常见的肌肉骨骼疾病,而肩袖疾病,特别是冈上肌腱撕裂,是最常见的原因之一。 保守性康复治疗,包括治疗性锻炼和物理治疗模式,被认为是部分性冈上肌腱撕裂的一线治疗方法。 近年来,基于虚拟现实(VR)的康复治疗已成为一种有前景的方法,可提高患者参与度并提供任务导向的锻炼环境。
这项随机对照研究的目的是调查VR辅助康复对部分性冈上肌腱撕裂患者的疼痛、运动恐惧症、生活质量和冈上肌腱厚度的影响。
49名年龄在18-65岁、经MRI确诊为部分性冈上肌腱撕裂的患者被随机分配到VR辅助康复组或常规锻炼组。 所有参与者均接受了为期三周的常规物理治疗方案,包括热敷、超声治疗、经皮神经电刺激和拉伸锻炼。 实验组还使用Meta Quest Pro头显进行了基于VR的锻炼。
结果指标包括通过数字评分量表评估的疼痛强度、肩关节活动范围、通过肩痛与残疾指数测量的功能状态、使用坦帕运动恐惧症量表评估的运动恐惧症、通过SF-36问卷测量的健康相关生活质量,以及通过超声检查评估的冈上肌腱厚度。 评估在干预前后进行。
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
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Çorum
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Çorum、Çorum、土耳其(türkiye)、19000
- Hitit University Erol Olçok Research Hospital Physical Medicine and Rehabilitation Clinic
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参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
纳入标准:18-65岁,肩痛持续超过4周,并经肩部磁共振成像确诊为冈上肌腱部分撕裂
排除标准:若参与者在过去六个月内接受过物理治疗或肩部注射、曾进行肌腱修复手术、存在沟通或认知问题、患有眩晕、前庭功能障碍或其他导致平衡不稳定的疾病、有癫痫或惊厥病史、对光敏感、确诊患有包括焦虑症或幽闭恐惧症在内的精神障碍、存在影响同一肩部的其他骨科疾病、处于孕期或哺乳期,或患有可能限制功能能力的神经、血管或心脏疾病,则予以排除
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
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实验性的:virtual reality group
Participants received the same physical therapy modalities as the control group, consisting of hot pack, therapeutic ultrasound, and transcutaneous electrical nerve stimulation.
They subsequently performed approximately 30 minutes of immersive virtual reality-based upper-extremity exercise using a Meta Quest Pro headset instead of the conventional therapeutic exercise component.
The virtual reality exercise was therefore a replacement rather than an additional treatment.
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Participants received physical therapy modalities consisting of hot pack, therapeutic ultrasound, and transcutaneous electrical nerve stimulation.
They subsequently performed approximately 30 minutes of immersive virtual reality-based upper-extremity exercise using a Meta Quest Pro headset instead of the conventional therapeutic shoulder exercise component.
The virtual reality activities involved repetitive, task-oriented shoulder and upper-extremity movements within an interactive three-dimensional environment.
The intervention was delivered five days per week for three weeks, for a total of 15 sessions.
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有源比较器:Control Group
Participants received physical therapy modalities consisting of hot pack, therapeutic ultrasound, and transcutaneous electrical nerve stimulation.
They subsequently performed approximately 30 minutes of supervised conventional therapeutic shoulder exercises targeting shoulder mobility, stretching, strengthening, and scapular stabilization.
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After receiving physical therapy modalities consisting of hot pack, therapeutic ultrasound, and transcutaneous electrical nerve stimulation, participants performed approximately 30 minutes of supervised conventional therapeutic shoulder exercise.
The program included scapular mobilization; stretching exercises for shoulder flexion, abduction, internal rotation, and external rotation; and strengthening exercises for the shoulder and scapular stabilizer muscles.
Exercises were performed in three sets of 10 repetitions.
The intervention was delivered five days per week for three weeks, for a total of 15 sessions.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
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Pain intensity measured by the Numeric Rating Scale (NRS)
大体时间:Baseline and after 3 weeks of treatment
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Pain intensity at rest and during shoulder movement was assessed separately using an 11-point Numeric Rating Scale, ranging from 0 (no pain) to 10 (the worst pain imaginable).
Higher scores indicated greater pain intensity.
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Baseline and after 3 weeks of treatment
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Passive range of motion (ROM) of the affected shoulder
大体时间:Baseline and after 3 weeks of treatment
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Passive range of motion of the affected shoulder, including flexion, extension, abduction, internal rotation, and external rotation, was measured in degrees using a Saehan goniometer.
Higher values indicated greater range of motion.
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Baseline and after 3 weeks of treatment
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Shoulder pain and disability measured using the Shoulder Pain and Disability Index (SPADI)
大体时间:Baseline and after 3 weeks of treatment
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The Shoulder Pain and Disability Index is a 13-item questionnaire comprising a five-item pain subscale and an eight-item disability subscale.
Pain, disability, and total scores are expressed on a scale from 0 to 100, with higher scores indicating greater pain and disability.
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Baseline and after 3 weeks of treatment
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Health-related quality of life measured using the Short Form-36 (SF-36)
大体时间:Baseline and after 3 weeks of treatment
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The Short Form-36 is a 36-item questionnaire comprising eight domains: physical functioning, role limitations due to physical health, bodily pain, general health, vitality, social functioning, role limitations due to emotional problems, and mental health.
Each domain is scored from 0 to 100, with higher scores indicating better health status.
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Baseline and after 3 weeks of treatment
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Kinesiophobia measured using the Tampa Scale of Kinesiophobia
大体时间:Baseline and after 3 weeks of treatment
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The Tampa Scale of Kinesiophobia is a 17-item questionnaire scored using a four-point Likert scale.
Total scores range from 17 to 68, with higher scores indicating greater fear of movement or reinjury.
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Baseline and after 3 weeks of treatment
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Supraspinatus tendon thickness measured using ultrasonography (USG)
大体时间:Baseline and after 3 weeks of treatment
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Supraspinatus tendon thickness was measured with the participant seated and the affected arm placed in the modified Crass position.
Using a Logiq V2 portable ultrasound device, the transducer was positioned longitudinally over the supraspinatus tendon, and tendon thickness was measured at the point of maximal thickness and recorded in centimeters.
The measurement procedure was based on the EURO-MUSCULUS shoulder scanning protocol.
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Baseline and after 3 weeks of treatment
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合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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