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New treatment option for Cervical Radiculopathy
Official title Effect of Kinetic Control Retraining on Neck Proprioception and Functional Outcome in Patients With Cervical Radiculopathy
ClinicalTrials.gov ID: NCT06803134
What this study is testing
- What it's testing
- The aim of this study is to investigate the effect of kinetic control retraining on neck proprioception and functional outcome in patients with cervical radiculopathy.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 40 to 55
You may be able to join if
- 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)..
You likely can't join if
- 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.
See the full eligibility 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)..
- 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.
The study team makes the final eligibility decision.
Where it's taking place
- Damietta, Egypt
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 40 years to 55 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Damietta, Egypt. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.