- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07321119
Correlation Between Cervical Deep Flexors Endurance and Proprioception Function in Cervical Radiculopathy
Correlation Between Endurance and Proprioception Function in Cervical Radiculopathy
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
In patients with cervical radiculopathy, endurance of the deep cervical flexor muscles (longus capitis and longus colli) plays a crucial role in maintaining cervical segmental stability and accurate sensorimotor control. These muscles are rich in muscle spindles and provide continuous afferent input necessary for cervical proprioception, including joint position sense and movement accuracy. When deep cervical flexor endurance is reduced, there is increased reliance on superficial neck muscles, leading to altered motor patterns and diminished quality of proprioceptive feedback.
Cervical radiculopathy further disrupts proprioceptive function through nerve root compression, inflammation, and impaired neural conduction, which affect both sensory input and motor output. This neuromuscular dysfunction results in increased joint position errors, delayed muscle activation, and poor postural control. Consequently, a significant correlation is observed between decreased deep cervical flexor endurance and impaired cervical proprioception, suggesting that deficits in muscle endurance contribute directly to sensorimotor dysfunction. These findings support rehabilitation approaches that emphasize endurance training of the deep cervical flexors to restore proprioceptive accuracy and cervical motor control in patients with cervical radiculopathy.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: ibrahim A abu ella, Phd
- Phone Number: +201008442281
- Email: ibrahimneuron@gmail.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
The study population consisted of 80 patients with cervical radiculopathy recruited from outpatient physical therapy clinics. Participants were adults of both sexes, aged between 20 and 60 years, presenting with neck pain associated with unilateral or bilateral upper limb radicular symptoms, including pain, numbness, or weakness. Cervical radiculopathy was diagnosed based on clinical examination findings such as dermatomal pain distribution, positive cervical compression tests, and neurological deficits, with imaging confirmation when available.
All participants were in the subacute to chronic stage of the condition and were able to sit independently and follow verbal instructions during assessment. Patients with a history of cervical spine surgery, recent trauma, vestibular disorders, or other neurological or systemic conditions affecting cervical proprioception were excluded. This population was selected to investigate the relationship between cervical deep flexor endurance and cerv
Description
Inclusion Criteria:
- Adults diagnosed with cervical radiculopathy based on clinical examination (± imaging confirmation).
Presence of neck pain with radiating symptoms to the upper limb for at least 4 weeks.
Age range 20-60 years.
Ability to understand instructions and participate in cervical endurance and proprioception assessments.
Exclusion Criteria:
- History of cervical spine surgery or acute cervical trauma.
Presence of neurological disorders other than cervical radiculopathy (e.g., stroke, multiple sclerosis).
Vestibular disorders or conditions affecting balance and head position sense.
Inflammatory, rheumatologic, or severe musculoskeletal conditions involving the cervical spine.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cervical proprioception errors by using joint position sense via CROM device
Time Frame: baseline
|
Cervical proprioception was assessed using the CROM device by measuring joint position sense error.
Participants were seated upright with the trunk stabilized and the CROM mounted on the head; visual input was eliminated by closing the eyes.
From a neutral head position, participants actively moved the head to a predetermined target angle (approximately 50-60% of available cervical range of motion) in flexion, extension, or rotation, held the position briefly, returned to neutral, and then attempted to reproduce the target position.
The absolute difference between the target and reproduced angles, recorded in degrees by the CROM, represented the joint position error, and the mean of three trials for each movement direction was used for analy
|
baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Deep flexor cervical muscle endurance using biofeedback device
Time Frame: baseline
|
Deep cervical flexor muscle endurance was assessed using a pressure biofeedback unit.
Participants were positioned in crook-lying with the pressure cuff placed suboccipitally and inflated to a baseline pressure of 20 mmHg.
After instruction and practice of the craniocervical flexion action, participants were asked to incrementally increase and maintain pressure (22-30 mmHg) by performing a gentle nodding movement without activation of superficial neck muscles.
Endurance was recorded as the maximum pressure level that could be held steadily for 10 seconds with correct technique, and the total performance score was determined based on the highest successfully maintained pressure level.
|
baseline
|
Collaborators and Investigators
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- trial registry 3
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Cervical Radiculopathy
-
Zonguldak Bulent Ecevit UniversityNot yet recruitingCervical Radiculopathy | Cervical Radiculopathy at C5 Nerve Root | Cervical Radiculopathy at C6 Nerve Root | Cervical Radiculopathy at C7 Nerve RootTurkey (Türkiye)
-
Elite College of Management Sciences, Gujranwala...CompletedCervical Radiculopathy | Cervical Radicular PainPakistan
-
Riphah International UniversityCompletedCervical Radiculopathy | CervicalPakistan
-
Guang'anmen Hospital of China Academy of Chinese...Not yet recruitingCervical Spondylotic Radiculopathy
-
Cairo UniversityCompletedCervical Radiculopathy | Disc Herniation | Cervical Radiculopathy at C5 Nerve Root | Cervical Radiculopathy at C6 Nerve Root | Cervical Radiculopathy at C7 Nerve RootEgypt
-
Marmara UniversityRecruitingCervical Radiculopathy | Cervical Radicular Pain | ProprioceptionTurkey (Türkiye)
-
William Beaumont HospitalsCamber Spine TechnologiesTerminatedCervical Radiculopathy | Cervical Disc DiseaseUnited States
-
Gazi UniversityRecruitingCervical Radiculopathy | Cervical Radicular Pain | Cervical Radiculitis | Cervical Root SyndromeTurkey
-
Pusan National University Yangsan HospitalActive, not recruitingCervical RadiculopathySouth Korea
-
Istanbul Medeniyet UniversityCompletedCervical RadiculopathyTurkey (Türkiye)
Clinical Trials on cevical range of motion device
-
Washington University School of MedicineNeurolutions, Inc.TerminatedHemiparesis | Chronic StrokeUnited States
-
Baylor College of MedicineActive, not recruitingPatellar DislocationUnited States
-
Mayo ClinicWithdrawnCubital Tunnel Syndrome
-
Riphah International UniversityActive, not recruiting
-
University of TorontoCanadian Orthopaedic Foundation; Orthopaedic Trauma Association; Künzli SwissSchuhUnknown
-
Balgrist University HospitalMaastricht UniversityCompleted
-
Istanbul UniversityCompleted
-
The Cooper Health SystemRecruitingProximal Humeral Fracture | Reverse Total Shoulder ArthroplastyUnited States
-
Istituto Ortopedico RizzoliCompletedStiffness of Knee, Not Elsewhere Classified | Knee FracturesItaly
-
Istanbul Medipol University HospitalCompletedChildren With CancerTurkey