This randomized clinical trial was conducted on patients with CTS who were referred to the specialized physical medicine and rehabilitation clinic at Birjand University of Medical Sciences. This study was registered in the Iranian Registry of Clinical Trials (IRCT) (clinical trial registration code:
IRCT20190618043934N23). The inclusion criteria were patients suffering from CTS with a mild to moderate form of the disease based on electrodiagnostic criteria, no use of non-steroidal anti-inflammatory drugs (NSAIDs) or steroids during the intervention, and a stable mental state to participate in the study. The exclusion criteria included pregnancy, previous treatment with ultrasound or laser, regular use of painkillers and anti-inflammatory medications, use of local steroid injections inside the carpal tunnel within the last year or during the study, severe atrophy of the thenar region, a history of malignant tumors, peripheral system neuropathies, and irregular attendance during the treatment process (
Figure 1). The sample size was calculated using the study conducted by Atya and Mansour (
24) and the following formula. Considering the time-consuming process of treatment, the need for patient follow-up, prevention of heterogeneity in the study groups, and accounting for a 20% dropout rate, the sample size in each group was estimated to be 24 hands/patients.
The study involved 48 hands/patients with CTS. Using a simple randomization method and a random number table, participants were allocated into two groups: Ultrasound (24 hands/patients) and neural-gliding techniques (24 hands/patients). A checklist was used to obtain demographic information, weight, height, dominant hand, history of underlying disease, duration of CTS symptoms, severity of the disease (mild or moderate), distal motor and sensory latency of the median nerve before and after the intervention, pain intensity score before and after the intervention, severity of symptoms (feeling of pain and paresthesia), and functional status before and after the intervention.
Performing median nerve gliding exercises can help alleviate pain, improve grip strength, and enhance performance for individuals suffering from CTS. Long-term ischemia can make nerves sensitive and lead to damage due to a lack of proper oxygenation. Neuromobilization can effectively reduce ischemia in the canal area, improve oxygenation, and lower pain and sensory-motor symptoms in CTS sufferers. Additionally, this technique helps the nerves regain their normal range of motion, reducing nerve adhesion and ischemic pain by improving oxygenation in the nerve.
One group was treated with pulsed ultrasound at a frequency of 1 MHz, with a current intensity of 1 watt/cm2, applied three times a week for 10 sessions, each session lasting 5 minutes. The second group underwent neural-gliding interventions three times a week for 10 sessions. Both groups were taught standard treatment, including the use of a wrist splint. Distal motor and sensory latency of the median nerve was determined using electromyography (EMG) and nerve conduction studies (NCS) before the interventions.
Evaluation of pain intensity was conducted using the VAS criteria before interventions, and the BOSTON Questionnaire was completed to assess the intensity of symptoms (pain and paresthesia) and the functional status of the patient. The questionnaire consists of two parts: The first part contains 11 questions to evaluate the severity of symptoms, and the second part has 8 questions to assess functional status. The questionnaire is scored on a 5-point Likert Scale.
The severity of symptoms dimension (questions 1 - 11) and the functional status dimension (questions 12 - 19) were interpreted as follows:
- Severity of symptoms: Non-symptomatic (1 - 11), mild (12 - 22), moderate (23 - 33), severe (34 - 44), and very severe (45 - 55).
- Functional status: Normal (less than 8), mild (9 - 16), moderate (17 - 24), severe (25 - 32), and very severe (33 - 40).
Following the interventions, distal motor and sensory latency of the median nerve was re-evaluated using NCS, along with the VAS criteria and the BOSTON Questionnaire. All collected data were entered into IBM SPSS Statistics for Windows, version 22 (IBM Corp., Armonk, N.Y., USA). Descriptive statistical indices (central tendency and dispersion) were used to report descriptive data. The Shapiro-Wilk test was employed to check normality. Mann-Whitney and Wilcoxon tests, chi-square, or Fisher's exact tests were utilized for analysis. The significance level for this study was set at P < 0.05.