Correlation Between Cervical Deep Flexors Endurance and Proprioception Function in Cervical Radiculopathy

December 26, 2025 updated by: Ibrahim Ahmed Ibrahim Abu Ella, Delta University for Science and Technology

Correlation Between Endurance and Proprioception Function in Cervical Radiculopathy

In cervical radiculopathy, reduced endurance of the deep cervical flexor muscles is associated with impaired cervical proprioception. This relationship reflects altered sensorimotor control due to muscle dysfunction and neural compromise, emphasizing the need for deep flexor endurance training in rehabilitation.

Study Overview

Status

Not yet recruiting

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

Observational

Enrollment (Estimated)

80

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

January 1, 2026

Primary Completion (Estimated)

February 1, 2026

Study Completion (Estimated)

March 1, 2026

Study Registration Dates

First Submitted

December 13, 2025

First Submitted That Met QC Criteria

December 26, 2025

First Posted (Actual)

January 6, 2026

Study Record Updates

Last Update Posted (Actual)

January 6, 2026

Last Update Submitted That Met QC Criteria

December 26, 2025

Last Verified

December 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • trial registry 3

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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.

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