- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07302282
The Effectiveness of Pain Neuroscience Education for Patients With Carpal Tunnel Syndrome
The Effectiveness of Pain Neuroscience Education for Patients With Mild to Moderate Carpal Tunnel Syndrome
The goal of this clinical trial is to investigate the effects of Pain Neuroscience Education applied in the treatment of mild and moderate carpal tunnel syndrome (CTS).
The main question it aims to answer is: Does PNE have a therapeutic effect on carpal tunnel syndrome in clinical and ultrasonographic terms? Researchers will compare whether PNE creates a synergistic effect alongside home based exercise programs and splint application in mild to moderate CTS, and will objectively demonstrate potential benefits such as relief from pain and numbness.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Carpal Tunnel Syndrome (CTS) is a common compressive neuropathy of the median nerve that presents with symptoms of numbness and tingling in the median nerve distribution of the hand. If symptoms are not treated early, they become chronic. Factors affecting the severity of chronic pain include; biological, psychological and social/environmental etc.
Pain neuroscience education is a treatment strategy that aims to teach patients about the effects of their beliefs and behaviors on the formation of their pain experiences. This education focuses on the role of the central nervous system in pain by raising awareness about the neurobiology and neurophysiology of pain. It focuses on remodelling the behavioral approach to pain perception rather than anatomical damage. This approach aims to reduce patients' fear and catastrophizing by helping them better understand pain. Various metaphors, examples, and visuals are used during PNE to help patients understand pain mechanisms. PNE is thought to have an impact not only on pain but also on disability, functionality, and quality of life. PNE has been documented to have a positive effect not only on pain but also on other important factors such as disability, functionality, and quality of life.
A clinical study has shown that adding PNE to a telerehabilitation program has some positive effects, such as a reduction in symptom severity in patients with carpal tunnel syndrome. However, the number of studies in the literature on the efficacy of PNE in carpal tunnel syndrome is limited to a single study and is based on subjective methods such as patient statements. Unlike the previous study, this study will use objective and innovative assessment methods such as ultrasonography, quantitative sensory test and examination to evaluate symptoms and function.
The evaluation methods used in the study will enable a more in-depth and reliable analysis of symptom management and recovery processes, thereby facilitating the collection of more accurate and reliable data. As there are no similar studies using objective evaluation methods, the methodological contributions of this study will be highly valuable. By offering an innovative approach to pain management and rehabilitation through conservative treatment, it will make significant contributions to both scientific literature and clinical practice.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Mahmut Talha Susam, MD.
- Phone Number: 90 5458445753
- Email: mahmuttalhasusam@kmu.edu.tr
Study Locations
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Karaman
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Karaman, Karaman, Turkey (Türkiye), 70200
- Recruiting
- Karaman Training and Research Hospital
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Contact:
- Mahmut Talha Susam, MD
- Phone Number: 90 5458445752
- Email: mahmuttalhasusam@kmu.edu.tr
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Being 18 years of age or older
- Having a diagnosis of mild or moderate CTS confirmed by ENMG
- Having complaints of pain and numbness in the first three fingers of the hand for at least 3 months
Exclusion Criteria:
- Presence of severe CTS findings on electrophysiological examination
- Presence of metabolic diseases such as uncontrolled diabetes and hypothyroidism
- Presence of inflammatory rheumatic disease (e.g., rheumatoid arthritis)
- Presence of other neuromuscular diseases affecting the hand and wrist (Polyneuropathy, Cervical radiculopathy, peripheral nerve damage, Brachial plexus damage, other entrapment neuropathies, etc.)
- History of hand and wrist trauma
- History of neck and wrist surgery
- History of steroid injection into the carpal tunnel within the last 3 months
- History of physical therapy application to wrist within the last 3 months
- Deformity preventing the use of a splint on the wrist
- Previous participation in a program for the psychological management of chronic pain
- Cognitive dysfunction preventing cooperation with tests
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Group 1 (home based exercise program)
Group 1 will receive training on median nerve gliding exercises and self-stretching exercises for the carpal ligament.
Patients will be asked to perform 3 sets of median nerve gliding exercises, each consisting of 10 repetitions, and self-stretching exercises for the carpal ligament 3 times a day for 30 seconds as part of home program.
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Stretching the transverse carpal ligament helps correct imbalance and provides more space for the median nerve, supporting nerve mobility. Stretching also balances flexor and extensor muscles, reduces tension, and supports overall hand health. Nerve gliding exercises, similar to stretching, aim to restore nerve mobility and reduce symptoms.
Other Names:
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Experimental: Group 2 (home based exercise program and pain neuroscience education)
Group 2 will receive exercise and pain neuroscience education.
The exercise will be taught as a home program, similar to the other group.
Pain neuroscience training will be provided twice a week for a total of 6 sessions by a trained physical therapist.
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Stretching the transverse carpal ligament helps correct imbalance and provides more space for the median nerve, supporting nerve mobility. Stretching also balances flexor and extensor muscles, reduces tension, and supports overall hand health. Nerve gliding exercises, similar to stretching, aim to restore nerve mobility and reduce symptoms.
Other Names:
PNE is an educational intervention aiming to alter a patient's beliefs and cognitions regarding their pain experience.
The main contents addressed in the educational session were: neurophysiological aspects of pain, biopsychosocial aspects of pain, concept of peripheral and central sensitization, using audio-visual support, examples and metaphors for a better understanding by the patient, as reported in previous studies.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Boston Carpal Tunnel Questionnaire - Symptom Severity Scale
Time Frame: Baseline, in the 3rd week and in the 6th week
|
Symptom Severity Scale is an 11-item questionnaire used to assess symptom severity in individuals with CTS.
Each item is scored from 1 to 5. Scores range from 1 (no symptoms) to 5 (worst symptoms).
The patient's symptom severity score is the average score of 11 items.
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Baseline, in the 3rd week and in the 6th week
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Boston Carpal Tunnel Questionnaire - Functional Status Scale
Time Frame: Baseline, in the 3rd week and in the 6th week
|
Functional Status Scale is an 8-item questionnaire used to assess the functional status of patients with CTS.
Each item is scored from 1 to 5. Scores range from 1 (no functional deficit) to 5 (worst possible function).
The patient's functional status score is the average of all 8 items.
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Baseline, in the 3rd week and in the 6th week
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Numerical Rating Scale
Time Frame: Baseline, in the 3rd week and in the 6th week
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Patients rate the current pain intensity from 0 ("no pain") to 10 ("worst possible pain").
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Baseline, in the 3rd week and in the 6th week
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6-item carpal tunnel syndrome symptom scale (CTS-6)
Time Frame: Baseline, in the 3rd week and in the 6th week
|
6 items are evaluated out of a total of 26 points.
If the patient's total score is above 5, the probability of carpal tunnel syndrome is 25%, while if it is above 12, the probability reaches 80%.
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Baseline, in the 3rd week and in the 6th week
|
|
Leeds Assessment of Neuropathic Symptoms and Signs (LANSS)
Time Frame: Baseline, in the 3rd week and in the 6th week
|
It consists of a total of 7 items.
The scale is scored between 0 and 24, with a score of 12 or higher suggesting neuropathic pain.
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Baseline, in the 3rd week and in the 6th week
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Ultrasound median nerve cross-sectional area
Time Frame: Baseline, in the 3rd week and in the 6th week
|
The cross-sectional area of the median nerve is significantly higher in CTS patients compared to the normal population.
Ultrasound, which is used to evaluate the median nerve and determine the underlying etiology, is also used to monitor the effectiveness of the treatment.
The cross-sectional area measurement of the median nerve will be recorded in mm².
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Baseline, in the 3rd week and in the 6th week
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Semmes-Weinstein Monofilament Test
Time Frame: Baseline, in the 3rd week and in the 6th week
|
It is used to assess light touch sensation.
The assessment is performed using 5 separate monofilaments.
The numerical value in the test kits represents the logarithm of 10 times the force required to bend the monofilament, expressed in milligrams.
The numerical values are 2.83 (normal light touch sensation), 3.61 (decreased light touch), 4.31 (decreased protective sensation), 4.56 (loss of protective sensation), and 6.65 (loss of deep pressure sensation).
The test is performed by applying the monofilament to the tip of the index finger at a 90-degree angle to the skin for 1.5 seconds, repeated three times.
The patient must perceive at least one of the monofilament applications as normal.
Failure to perceive the 2.83 threshold value is significant for carpal tunnel syndrome.
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Baseline, in the 3rd week and in the 6th week
|
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Two-Point Discrimination Test (2PD)
Time Frame: Baseline, in the 3rd week and in the 6th week
|
It is used to assess cortical tactile sensation.
The test is applied to the lateral part of the volar surface of the index finger tip.
During the test, patients are asked to close their eyes and indicate whether they feel a single or double point.
To prevent incorrect sensory perception, pressure exceeding 1 mm is not applied to the skin.
The distance between the two points is increased by 1 mm at a time, starting from 1 mm, until the patient feels two distinct points.
In the evaluation, a measurement value perceived as two points is considered normal if it is below 6 mm.
The minimum distance between two points that can be distinguished by an individual will be tested three times at 1-minute intervals, and the average value will be recorded in centimeters.
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Baseline, in the 3rd week and in the 6th week
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Quantitative sensory evaluation
Time Frame: Baseline, in the 3rd week and in the 6th week
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Starting at 32 °C, the Cold Detection Threshold is cooled at a rate of 1 °C per second, and the patient presses the button when they first feel the cold.
For the Heat Detection Threshold, the temperature is heated at a rate of 1 °C per second, and the patient presses the button when they first feel the heat.
For the cold pain threshold, it is cooled at a rate of 1 °C per second, and the patient presses the button when they feel cold pain.
For the hot pain threshold, it is heated at a rate of 1 °C per second, and the patient presses the button when they feel hot pain.
Each measurement is taken 3 times, and the average value is recorded in degrees Celsius.
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Baseline, in the 3rd week and in the 6th week
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Hand grip strength measurement
Time Frame: Baseline, in the 3rd week and in the 6th week
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The Baseline® hydraulic hand dynamometer-90 kg (Fabrication Enterprises, White Plains, New York 10602, USA) will be used for hand grip strength measurements.
According to the test procedure, three measurements will be taken for hand grip and finger grip strength, with one-minute intervals between each measurement, and the average peak force value will be recorded in kilograms.
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Baseline, in the 3rd week and in the 6th week
|
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Finger pinch strength measurement
Time Frame: Baseline, in the 3rd week and in the 6th week
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The Baseline® hydraulic pinchmeter (Fabrication Enterprises, USA) will be used for pinch force measurements.
According to the test procedure, three measurements will be taken for hand grip and finger grip strength, with one-minute intervals between each measurement, and the average peak force value will be recorded in kilograms.
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Baseline, in the 3rd week and in the 6th week
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Chair: Mahmut Talha Susam, MD, Karamanoglu Mehmetbey University Physical Medicine and Rehabilitation
- Principal Investigator: Mahmut Talha Susam, MD, Karamanoglu Mehmetbey University Physical Medicine and Rehabilitation
- Principal Investigator: Aynur Başaran, Prof.MD, Karamanoglu Mehmetbey University Physical Medicine and Rehabilitation
- Principal Investigator: Süleyman Gül, PhD, Karamanoglu Mehmetbey University Physical Medicine and Rehabilitation
- Principal Investigator: Elif Dilara Durmaz, Pt, Karaman Training and Research Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Nervous System Diseases
- Wounds and Injuries
- Neuromuscular Diseases
- Peripheral Nervous System Diseases
- Cumulative Trauma Disorders
- Sprains and Strains
- Behavior
- Nerve Compression Syndromes
- Carpal Tunnel Syndrome
- Median Neuropathy
- Mononeuropathies
- Motor Activity
- Motor Activity
- Movement
- Musculoskeletal Physiological Phenomena
- Musculoskeletal and Neural Physiological Phenomena
- Exercise
Other Study ID Numbers
- 25-2025/12
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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