Kinetic control retraining for neck pain relief in cervical radiculopathy patients
Effect of Kinetic Control Retraining on Neck Proprioception and Functional Outcome in Patients With Cervical Radiculopathy
This study is testing a special physical therapy program to see if it can help people aged 40-55 with neck pain from cervical radiculopathy feel better and move more easily.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 44 (estimated) |
| Ages | 40 Years to 55 Years |
| Sex | All |
| Sponsor | Cairo University Academic / other |
| Locations | 1 site (Damietta) |
| Trial ID | NCT06803134 on ClinicalTrials.gov |
What this trial studies
This study investigates the effects of kinetic control retraining on neck proprioception and functional outcomes in patients suffering from cervical radiculopathy. Cervical radiculopathy is often caused by degenerative changes leading to neck pain and radiating discomfort, significantly impacting patients' quality of life. The intervention involves a selected physical therapy program aimed at improving movement control and reducing pain through targeted exercises. The study will include patients aged 40-55 with chronic unilateral cervical radiculopathy and will assess the effectiveness of this non-pharmacological approach.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 40-55 with chronic unilateral cervical radiculopathy lasting between 3 months to 1 year.
Not a fit: Patients with cervical myelopathy, previous cervical or shoulder surgeries, or significant psychological issues may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve neck function and reduce pain for patients with cervical radiculopathy.
How similar studies have performed: While similar approaches have been explored, this specific intervention focusing on kinetic control retraining in cervical radiculopathy is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Forty Four patients suffering from chronic cervical unilateral radiculopathy (symptomatic duration) (3 months to 1year). * Their age ranges 40-55 years, from both sexes. * Body mass index (BMI) of less than 30 Kg/m2 * Cervical spondylosis (at the levels of C5-C6/C6-C7 confirmed by cervical MRI).. Exclusion Criteria: * Cervical myelopathy with evidence of pyramidal, posterior column, and or spinothalamic tract lesions. * Patients with decreased range of motion of cervical spine secondary to congenital anomalies, musculature contracture, or bony block. * Previous cervical or shoulder surgery or trauma. * Cervical instability caused by structural problem (e.g. ligament tear or spondylolithesis. * Psychological problems interfering with the patient understanding of the orders, or patients who did not have direction preference. * Vertebro-basilar artery insufficiency, diabetic neuropathy. * Comorbidities that impact physical activity (e.g., cerebrovascular accidents, severe heart disease). - Double crush syndrome and thoracic outlet syndrome.
Where this trial is running
Damietta
- Horus University — Damietta, Egypt (Recruiting)
Study contacts
- Study coordinator: Ebtesam Wafik Osman Shehab El-Din, M.Sc
- Email: ebtsShehab96@gmail.com
- Phone: +20 10 01447604
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.