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Recruiting Not applicable

Investigation of the Effectiveness of Kinesiological Taping in Cubital Tunnel Syndrome

NCT07001111 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-04-21
Last updated
2025-09-12

Condition(s) studied

Cubital Tunnel SyndromeKinesio TapingUlnar Neuropathies

Investigational drug(s) / intervention(s)

kinesio tapingUlnar nerve mobilization exerciseSham (No Treatment)Numeric Rating Scale (NRS)the ulnar nerve cross-sectional area measured by ultrasoundNeuropathic pain scale (measured using the DN-4 scale)SF-12 Quality of Life ScaleQUICK-DASHGrip strength measured with a hand dynamometer

kinesio taping: Kinesio taping at the level of the cubital tunnel on the elbow

Ulnar nerve mobilization exercise: All patients will be provided with information and an exercise sheet containing pictures on ulnar nerve gliding exercises. To monitor whether patients are performing the exercises correctly, they will be asked to come to the hospital once a week, where they will perform the exercises under the supervision of a physiotherapist. In the exercise program, different positions will be held for 30 seconds, with a 1-minute rest between them, and the exercises will be performed twice a day .

Sham (No Treatment): It will be applied in the same way as kinesiological taping with adhesive tape.

Numeric Rating Scale (NRS): Description: To demonstrate that kinesiological taping will result in a reduction of pain intensity associated with Cubital Tunnel Syndrome, as measured by the Numeric Rating Scale (NRS) ranging from 0 to 10.

the ulnar nerve cross-sectional area measured by ultrasound: The measurements will be taken with the patient in a supine position, the affected arm in shoulder abduction and external rotation, and the elbow flexed at 70°-90°. After applying a generous amount of gel, the lateral edge of the ultrasound probe will be placed on the medial epicondyle, and the medial edge of the probe will be positioned on the olecranon; the ulnar nerve will be directly examined in the retroepicondylar groove. Once the nerve is visualized, the widest point will be identified, and cross-sectional area (CSA) measurements will be taken with the probe perpendicular to the nerve at the center of the screen . The measurements will be repeated twice, and the average will be calculated.

Neuropathic pain scale (measured using the DN-4 scale): The DN4 questionnaire consists of two main sections and a total of ten questions. The first section includes seven questions related to pain characteristics and sensory information obtained through patient interview. These questions are about burning, electric shocks, coldness, tingling, pricking, numbness, and itching. The second section contains three statements related to physical examination (touch hypoesthesia, pinprick hypoesthesia, and allodynia). For each statement, "yes" or "no" responses are given. A score of "1" is assigned for "yes" answers and "0" for "no" answers, and the scores are summed. A total score of 4 or more out of 12 is interpreted as neuropathic pain.

SF-12 Quality of Life Scale: The SF-12 Quality of Life Scale is a short form of the SF-36 Quality of Life Scale. While the SF-36 is used for chronic conditions (states), the SF-12 is used for short-term assessments (clinical findings). Similarly, it is also used to gather information about the patient's general health status. The SF-12 provides the same summary component scores as the SF-36, but with fewer items, making it a significant advantage due to its shorter application time. The scale asks the patient about their health opinions, how they feel, and how easily they can perform their usual activities. Scores range from 0 to 100, with higher scores indicating better quality of life.

QUICK-DASH: QUICK-DASH (Shoulder, Arm, and Hand Problems Questionnaire): This questionnaire assesses both the ability to perform certain physical activities as well as the symptoms of the disease. Each question is answered based on the condition of the past week, and the appropriate score is marked. The answer is given based solely on the ability to perform the physical activity, without considering which hand or arm is injured. Scoring: 1. = No difficulty 2. = Mild difficulty 3. = Moderate difficulty 4. = Severe difficulty 5. = Unable to perform QUICK DASH DISABILITY/SYMPTOM SCORE: (\[(n total score\] - 1) x 25; where n represents the number of questions answered. If more than one question is unanswered, the Quick DASH score cannot be calculated. SCORE FOR OPTIONAL MODELS: For each model, divide the total score by 4, subtract 1, and multiply by 25. If more than one question is unanswered, the score for optional models cannot be calculated. Based on the results of the questionnaire, a score b

Grip strength measured with a hand dynamometer: Grip strength will be measured using a hand dynamometer, with the average of three measurements taken, each followed by a 30-second rest period.

Study summary

This study aims to investigate the effect of kinesiological taping, applied in addition to exercise, on clinical symptoms in patients diagnosed with Cubital Tunnel Syndrome. The patients will be randomized into three groups (exercise, exercise + kinesiological taping, exercise + sham taping) and will be evaluated at the 1st and 3rd months after a 3-week treatment period.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Aged between 18 and 65 years * Patients with at least 3 points of pain according to the Numeric Rating Scale (NRS) * Patients diagnosed with Cubital Tunnel Syndrome via Electroneuromyography (ENMG) * Literate * Willing to consent to participate in the study Exclusion Criteria: * Having any secondary entrapment neuropathy such as diabetes, inflammatory arthritis, or hypothyroidism * Pregnancy * Active cancer presence * Skin infection, burns, wounds, or scars on the forearm * History of elbow trauma * Cervical radiculopathy or brachial plexopathy * Polyneuropathy * Having previously undergone Cubital Tunnel decompression surgery * Having received a corticosteroid injection into the Cubital Tunnel within the last 3 months * Illiterate * Not consenting to participate in the study

Primary outcome measure(s)

  • Numeric Rating Scale (NRS) — 3 months
    To demonstrate that kinesiological taping will result in a reduction of pain intensity associated with Cubital Tunnel Syndrome, as measured by the Numeric Rating Scale (NRS) ranging from 0 to 10.

Trial sites (2)

FacilityCityRegionStatus
Health Sciences University Istanbul Uskudar Not Yet Recruiting
Sultan 2. Abdülhamid Han Eğitim ve Araştırma Hastanesi Istanbul Üsküdar Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07001111 on ClinicalTrials.gov ↗ ← All trials in Turkey