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Carpal tunnel syndrome (CTS) is the most common entrapment neuropathy caused by compression of the median nerve at the wrist. Conservative interventions such as splinting and manual therapy are frequently used in individuals with mild-to-moderate CTS. Neurodynamic mobilization and carpal bone mobilization aim to improve neural and soft tissue mobility; however, their comparative effects on clinical outcomes and median nerve morphology are not fully understood.
This interventional, non-randomized clinical study aims to compare the clinical and ultrasonographic effects of neurodynamic mobilization plus splinting, carpal bone mobilization plus splinting, and splinting alone in patients with mild-to-moderate CTS. Ninety-three participants diagnosed with mild-to-moderate carpal tunnel syndrome based on electrodiagnostic criteria will be included. Participants will be allocated into three parallel groups without randomization. All participants will receive a neutral-position wrist splint as standard conservative care.
Two intervention groups will additionally receive either neurodynamic mobilization exercises or carpal bone mobilization techniques administered by a physiotherapist for four weeks. Clinical outcomes and median nerve morphology will be evaluated at baseline and immediately after the intervention period.
The primary outcome is the change in the Boston Carpal Tunnel Questionnaire score. Secondary outcomes include pain intensity, neuropathic pain, functional disability, muscle strength, pressure pain threshold, and ultrasonographic measurements of the median nerve.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| neurodynamic mobs in addition splint | Experimental | Median nerve neurodynamic mobilization exercises administered by a physiotherapist for 4 weeks in addition to night-time wrist splint use |
|
| Carpal Bone Mobilization + Splint | Experimental | Carpal bone mobilization techniques administered by a physiotherapist for 4 weeks in addition to night-time wrist splint use. |
|
| Splint only | Active Comparator | Neutral-position wrist splint worn at night for 4 weeks. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Neurodynamic mobilization | Other | Median nerve neurodynamic mobilization exercises performed 5 sessions per week for 4 weeks. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Boston Carpal Tunnel Questionnaire (BCTQ) Total Score | Change in Boston Carpal Tunnel Questionnaire (BCTQ) Total Score | Baseline to 4 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Visual Analog Scale (VAS) | Pain intensity measured using a 10-cm visual analog scale. | Baseline to 4 weeks |
| Leeds Assessment of Neuropathic Symptoms and Signs (LANSS) | Change in Neuropathic Pain Score Assessed by Leeds Assessment of Neuropathic Symptoms and Signs (LANSS). |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Merve Akdeniz Leblebicier, MD | Contact | 00902742600043 | 4343 | merve1985akdeniz@hotmail.com |
| Esengül Alıcı, MD | Contact | 00902742600043 | 4343 | essengulalici@gmail.com |
| Name | Affiliation | Role |
|---|---|---|
| Merve Akdeniz Leblebicier, MD | Kutahya Health Sciences University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Kutahya Health Sciences University Yoncalı Physical Therapy and Rehabilitation Hospital | Kütahya | Yoncalı | 43000 | Turkey (Türkiye) |
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| ID | Term |
|---|---|
| D002349 | Carpal Tunnel Syndrome |
| ID | Term |
|---|---|
| D020423 | Median Neuropathy |
| D020422 | Mononeuropathies |
| D010523 | Peripheral Nervous System Diseases |
| D009468 | Neuromuscular Diseases |
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| ID | Term |
|---|---|
| D013165 | Splints |
| ID | Term |
|---|---|
| D016267 | External Fixators |
| D009984 | Orthopedic Fixation Devices |
| D009983 | Orthopedic Equipment |
| D013523 | Surgical Equipment |
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| Carpal bone mobilization | Other | Manual carpal bone mobilization techniques applied 5 sessions per week for 4 weeks. |
|
| Splint | Other | Neutral-position wrist splint used during night-time for 4 weeks. |
|
| Baseline to 4 weeks |
| Quick Disabilities of the Arm, Shoulder and Hand (QuickDASH) | Change in Upper Extremity Disability Assessed by Quick Disabilities of the Arm, Shoulder and Hand (QuickDASH). | Baseline to 4 weeks |
| Grip Strength | Change Grip strength measured using a Jamar dynamometer. | Baseline to 4 weeks |
| Pinch Strength | Change in Pinch Strength measured using a Pinchmeter. | Baseline to 4 weeks |
| Pressure Pain Threshold | Change in pressure pain threshold assessed using J -Tech algometer. | Baseline to 4 weeks |
| Median Nerve Cross-Sectional Area | Change in Median Nerve Cross-Sectional Area Assessed by Ultrasonography. | Baseline to 4 weeks |
| D009422 | Nervous System Diseases |
| D009408 | Nerve Compression Syndromes |
| D012090 | Cumulative Trauma Disorders |
| D013180 | Sprains and Strains |
| D014947 | Wounds and Injuries |
| D004864 |
| Equipment and Supplies |
| D053831 | Surgical Fixation Devices |