Assessment of Ultrasound Findings, Nerve Test Results, and Hand Function in Patients With Carpal Tunnel Syndrome
Association of Clinical Severity With Ultrasonographic, Electrophysiological, and Functional Parameters in Patients With Carpal Tunnel Syndrome: A Cross-Sectional Observational Study
Carpal tunnel syndrome is one of the most common conditions caused by compression of a nerve at the wrist. It can lead to numbness, tingling, pain, weakness, and difficulty performing daily activities. Although nerve conduction studies are widely used to confirm the diagnosis and assess disease severity, ultrasonography has become an increasingly important, non-invasive diagnostic tool. However, the relationship between ultrasound findings, nerve conduction study results, hand function, and symptom severity has not been fully clarified.
The purpose of this study is to investigate the relationship between the clinical severity of carpal tunnel syndrome and ultrasonographic, electrophysiological, and functional parameters. Participants with carpal tunnel syndrome will undergo ultrasonographic measurement of the median nerve, nerve conduction studies, hand grip strength assessment, pressure pain threshold measurement, and completion of the Boston Carpal Tunnel Questionnaire.
The investigators hypothesize that greater clinical severity will be associated with larger median nerve cross-sectional area, more severe electrophysiological abnormalities, reduced hand grip strength, lower pressure pain threshold, and poorer functional status. The findings of this study may improve the understanding of the relationship between structural, electrophysiological, and functional changes in carpal tunnel syndrome and contribute to clinical evaluation and patient management.
研究概览
研究类型
注册 (实际的)
联系人和位置
学习地点
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Istanbul
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Küçükçekmece、Istanbul、土耳其(türkiye)、34307
- Kanuni Sultan Suleyman Education and Research Hospital
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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
取样方法
研究人群
描述
Inclusion Criteria:
- Adults aged 18 years or older
- Clinical findings consistent with carpal tunnel syndrome
- Carpal tunnel syndrome confirmed by electroneuromyography
- Ability to understand and complete the study assessments
- Provision of written informed consent
Exclusion Criteria:
- Previous carpal tunnel release surgery
- History of fracture, major trauma, or surgery involving the assessed wrist or hand
- Cervical radiculopathy, brachial plexopathy, or other peripheral neuropathy affecting the upper extremity
- Polyneuropathy
- Inflammatory rheumatic disease or active infection involving the assessed upper extremity
- Severe neurological or musculoskeletal disorder that may affect hand function
- Inability to complete ultrasonographic, electrophysiological, functional, or questionnaire assessments
学习计划
研究是如何设计的?
设计细节
队列和干预
团体/队列 |
干预/治疗 |
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Mild Carpal Tunnel Syndrome
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Participants will undergo a standardized diagnostic assessment including ultrasonographic measurement of the median nerve cross-sectional area at the carpal tunnel inlet, nerve conduction study evaluation, hand grip strength measurement using a Jamar dynamometer, pressure pain threshold assessment using a digital algometer, and completion of the Boston Carpal Tunnel Questionnaire.
All assessments will be performed once during a single study visit.
No therapeutic intervention will be administered.
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Moderate Carpal Tunnel Syndrome
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Participants will undergo a standardized diagnostic assessment including ultrasonographic measurement of the median nerve cross-sectional area at the carpal tunnel inlet, nerve conduction study evaluation, hand grip strength measurement using a Jamar dynamometer, pressure pain threshold assessment using a digital algometer, and completion of the Boston Carpal Tunnel Questionnaire.
All assessments will be performed once during a single study visit.
No therapeutic intervention will be administered.
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Severe Carpal Tunnel Syndrome
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Participants will undergo a standardized diagnostic assessment including ultrasonographic measurement of the median nerve cross-sectional area at the carpal tunnel inlet, nerve conduction study evaluation, hand grip strength measurement using a Jamar dynamometer, pressure pain threshold assessment using a digital algometer, and completion of the Boston Carpal Tunnel Questionnaire.
All assessments will be performed once during a single study visit.
No therapeutic intervention will be administered.
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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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Median Nerve Cross-Sectional Area Measured by Ultrasonography (mm²)
大体时间:Baseline (prior to study assessments, during the single study visit)
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The median nerve cross-sectional area will be measured by high-resolution ultrasonography at the carpal tunnel inlet (pisiform level).
The mean of three measurements will be recorded in square millimeters (mm²).
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Baseline (prior to study assessments, during the single study visit)
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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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Boston Carpal Tunnel Questionnaire Symptom Severity Score
大体时间:Baseline (prior to study assessments, during the single study visit)
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Symptom severity will be assessed using the Boston Carpal Tunnel Questionnaire (BCTQ) Symptom Severity Scale.
Scores range from 1 to 5, with higher scores indicating greater symptom severity.
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Baseline (prior to study assessments, during the single study visit)
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Boston Carpal Tunnel Questionnaire Functional Status Score
大体时间:Baseline (prior to study assessments, during the single study visit)
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Functional status will be assessed using the Functional Status Scale of the Boston Carpal Tunnel Questionnaire (BCTQ-FSS).
The questionnaire consists of 8 items evaluating difficulty in performing daily activities.
Each item is scored from 1 (no difficulty) to 5 (cannot perform the activity), and the final score is calculated as the mean of all items.
Higher scores indicate greater functional impairment.
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Baseline (prior to study assessments, during the single study visit)
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Hand Grip Strength Measured Using a Jamar Dynamometer (kg)
大体时间:Baseline (prior to study assessments, during the single study visit)
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Maximum hand grip strength will be measured using a Jamar hydraulic hand dynamometer.
The mean of three measurements will be recorded in kilograms (kg).
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Baseline (prior to study assessments, during the single study visit)
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Pressure Pain Threshold Measured Using a Digital Algometer (kPa)
大体时间:Baseline (prior to study assessments, during the single study visit)
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Pressure pain threshold will be assessed using a digital pressure algometer.
The mean of three measurements will be recorded in kPa
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Baseline (prior to study assessments, during the single study visit)
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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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