Neuromuscular Re-education on Pain, ROM and Disability in Cervical Radiculopathy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age30-50
SponsorRiphah International University

About this trial

This study explores the effectiveness of Neuromuscular Re-education compared to conventional therapies in managing pain, range of motion, and disability in patients with Cervical Radiculopathy

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Participants of Age between 30 and 50 years old.

Participants of both gender included.

Participants having Unilateral upper extremity pain, paresthesia, or numbness

Positive Spurling's test

Disqualifiers

Participants having prior cervical spine surgery.

Participants with Cervical vertebral fracture

Participants with severe osteoporosis, rheumatic disease, shoulder disease, or infection will be excluded.

Participants with vertebro-basilar artery insufficiency and diabetic neuropathy

Trial design

Design model

Parallel

Treatments tested in this trial

  • Neuromuscular Re education

    Other intervention

    A. Postural training and functional task simulation(chin tuck, Shoulder blade squeeze, reaching, carrying, lifting tasks) Proprioceptive tasks( single leg stance with head movement), deep cervical strengthening. 3 sessions per week, 30 minutes per session (10 mint each component),10 repetition per set, 2 set, 10 second Resting interval Resting period: 1 mint to next exercise

  • Conventional Physical Therapy

    Other intervention

    * TENS and hot pack for 10 to 15 minutes * Manual therapy techniques (e.g., mobilizations grade II). 5 to 10 repetition * Cervical isometric exercises 10 reps * General education on posture and ergonomics guidelines * Frequency: 3 sessions per week * Duration: 50 minutes per session, 10 mint each component * Repetition: 10 repetition per set, 2 set , 10 second resting interval * Resting period: 1 mint to next exercise

Treatment groups

52 Participants
are divided into 2 treatment groups
Group A: Neuromuscular Re-education GroupExperimental treatment 1 intervention
Group B: Conventional Physical TherapyActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Goniometer

A goniometer is used to measure cervical range of motion (ROM) by aligning its fulcrum over a bony landmark (like the C7 vertebrae or external auditory meatus) and its arms with other bony landmarks (such as the nose, acromion, or sternal notch) to measure the angle of movement in degrees.

Time frame
8th Week
2

NDI (Neck Disability Index)

The NDI is a 10-item questionnaire that assesses how neck pain affects daily activities(28). The Neck Disability Index (NDI) measures neck-specific disability through a 10-item questionnaire assessing pain and daily activities like personal care, lifting, and concentration. Scores range from 0-50 (or 0-100%), with higher scores indicating greater disability

Time frame
8th week
3

Numeric Pain Rate Scale

The Numerical Pain Rating Scale (NPRS) has been used to assess the level of pain patients experience. It can be used to assess pain either verbally or through a self completion questionnaires. Patients are asked to circle a number on a scale that best describes the pain the experience. Patients are asked to recall from the pain scale from 0 to 10. 0 equals No pain, 1-3 equals Mild pain, 4-6 equals Moderate pain, 7-9 equals Severe pain, and 10 equals Very Severe pain. NPRS shows strong test-retest score even in illiterate and literate patients

Time frame
8th week

Secondary outcomes

Other outcomes

Sponsors and contacts

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