Effectiveness of Kinesiotaping and Peloidotherapy in Carpal Tunnel Syndrome
NCT ID: NCT06977321
Last Updated: 2025-07-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ENROLLING_BY_INVITATION
NA
90 participants
INTERVENTIONAL
2024-12-01
2025-12-31
Brief Summary
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Detailed Description
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Patients who were evaluated by detailed clinical examination and medical history according to the inclusion and exclusion criteria were given written informed consent and assigned to one of the three treatment groups using block randomization. Basic sociodemographic information (age, gender, body mass index, employment status, education level, marital status,etc) and clinical data (dominant hand, duration of symptoms, comorbidities, hand to be treated, Tinel/Phalen sign, pain intensity, baseline electrophysiological parameters) will be recorded. The first group will consist of patients who have received peloid therapy at 45 degrees for a total of 15 sessions of 20 minutes, 5 days a week for 3 weeks with a home-based exercise program. The second group will consist of patients who received a home-based exercise program with kinesiotaping for a total of 6 sessions 2 times a week. Patients who only received home-based exercise program will be included in the 3rd group. During the treatment period, patients will be allowed to take only paracetamol for pain, if necessary, except for the medications they use continuously for comorbid reasons.
All groups were evaluated by a blinded assessor based on examination findings (Tinel/Phalen tests), pain intensity (VAS), hand grip strength (HGS), finger pinch strength (FGS), the Turkish version of the Boston Carpal Tunnel Questionnaire, the 4-Question Neuropathic Pain Questionnaire (DN4), and ultrasound measurements (median nerve cross-sectional areas \[CSA\]) at the proximal insertion of the carpal tunnel (at the level of the scaphoid and pisiform bones and the distal wrist crease), both after treatment (three weeks/W3) and at three months post-treatment (W12).
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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Kinesiotaping
This group will be given a home exercise program along with a total of 6 sessions of kinesiotaping twice a week.
Kinesiotaping
Kinesiotaping, unlike wrist splints, which are frequently used in the treatment of carpal tunnel syndrome, does not restrict daily living activities. Space correction technique will be applied while performing kinesio taping.
Home exercise
Flexor tendon gliding exercises, median nerve gliding exercises, and isometric wrist strengthening exercises will be given as exercises.
Peloidotherapy
This group will consist of patients who have received peloid therapy for a total of 15 sessions of 20 minutes at 45 degrees for 3 weeks, 5 days a week, along with a home exercise program.
Peloidotherapy
Peloidotherapy stands out among superficial heating physical therapy modalities with its mineral and natural origin.
Home exercise
Flexor tendon gliding exercises, median nerve gliding exercises, and isometric wrist strengthening exercises will be given as exercises.
Home exercise
This group will consist of patients who have only been given a home exercise program. Flexor tendon gliding exercises, median nerve gliding exercises, and isometric wrist strengthening exercises will be given as exercises.
Home exercise
Flexor tendon gliding exercises, median nerve gliding exercises, and isometric wrist strengthening exercises will be given as exercises.
Interventions
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Kinesiotaping
Kinesiotaping, unlike wrist splints, which are frequently used in the treatment of carpal tunnel syndrome, does not restrict daily living activities. Space correction technique will be applied while performing kinesio taping.
Peloidotherapy
Peloidotherapy stands out among superficial heating physical therapy modalities with its mineral and natural origin.
Home exercise
Flexor tendon gliding exercises, median nerve gliding exercises, and isometric wrist strengthening exercises will be given as exercises.
Eligibility Criteria
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Inclusion Criteria
* Agreeing to participate voluntarily in the study
* Being diagnosed with mild or moderate idiopathic chronic CTS as a result of anamnesis, clinical examination and nerve conduction study
Exclusion Criteria
* Being diagnosed with severe CTS
* Having a history of previous wrist surgery or trauma
* Having atrophy in the thenar region or weakness in the thenar muscles
* Having cervical radiculopathy, thoracic outlet syndrome, polyneuropathy, brachial neuropathy or proximal median nerve neuropathy
* Having had steroid injections in the last 3 months and taking oral steroid medications
* Being pregnant
* Having an open wound or rash in the wrist and its surroundings that would prevent treatment
* Patients who are receiving or will receive another/additional treatment for CTS
* Patients with a bifid median nerve, persistent median artery, ganglion cyst, tenosynovitis, or tendinitis in the wrist.
18 Months
65 Months
ALL
No
Sponsors
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Konya Beyhekim Training and Research Hospital
OTHER_GOV
Responsible Party
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Ayşe Güleç
MD
Locations
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Konya Beyhekim Training and Research Hospital
Konya, , Turkey (Türkiye)
Countries
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Other Identifiers
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KonyaBeyhekimTRH19881991
Identifier Type: -
Identifier Source: org_study_id
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