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

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age30-45
SponsorDelta University for Science and Technology

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adults diagnosed with cervical radiculopathy based on clinical examination (± imaging confirmation).

Disqualifiers

History of cervical spine surgery or acute cervical trauma.

Trial 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

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

  • cevical range of motion device

    Device

    Cervical proprioception was evaluated using the Cervical Range of Motion (CROM) device by assessing joint position sense (JPS). With the participant seated in an upright position, the CROM device was securely fitted to the head. The patient was instructed to actively move the head from a neutral starting position into a specific direction (flexion, extension, rotation, or lateral flexion), then return to the perceived neutral position with eyes closed. The difference between the starting neutral position and the repositioned angle was recorded as the joint position error (JPE), measured in degrees. Multiple trials were performed for each movement direction, and the mean JPE value was calculated. Higher JPE values indicated poorer cervical proprioceptive accuracy. The CROM device is considered a reliable and valid clinical tool for quantifying cervical proprioception in patients with cervical radiculopathy.

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Cervical proprioception errors by using joint position sense via CROM device

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

Time frame
baseline

Secondary outcomes

1

Deep flexor cervical muscle endurance using biofeedback device

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.

Time frame
baseline

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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