Health TrialsbyHealthPanel

High Tone Power Therapy on Neck Pain and Proprioception in Cervical Radiculopathy

ConditionCervical Radiculopathy
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age35-50
SponsorOctober 6 University

About this trial

To investigate the Effect of High Tone Power Therapy on Neck Pain and Proprioception in Cervical Radiculopathy Patients.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Their ages range from 35 to 50 years.

Both sex

With mild to moderate cervical disability according to the neck disability index

Unilateral cervical radiculopathy for more than 6 months.

Disqualifiers

Any other musculoskeletal disorders of the spine or upper extremity

Patients with any other Neurological deficits, psychiatric disease Cervical myelopathy, Cognitive problems, vertebral fractures and previous history of spine or cervical surgery.

Neck pain with vertigo or with bilateral upper limbs referred pain.

Clinical instability, recent trauma and vertebrobasilar insufficiency.

Trial design

Design model

Parallel

Treatments tested in this trial

  • selected exercise program

    Other intervention

    therapeutic ultrasound, Static neck exercise

  • High Tone Power Therapy

    Device

    High Tone Power Therapy delivered in cervical region 3 times per week for four weeks

Treatment groups

42 Participants
are divided into 2 treatment groups
Group A: study groupOther 2 interventions
Group B: control groupOther 1 intervention

Trial outcomes

Primary outcomes

1

cervical joint position error test

The subject will be instructed to perform an active head rotation to one side, after which returns back to the neutral or starting head position. The test will be performed in a 3 trials in each direction

Time frame
four weeks
2

Neck disability index

includes 10 items as follows: Pain Intensity, Personal Care, Lifting, Reading, Headaches, Concentration, Work, Driving, Sleeping, and Recreation, with a score (0:5) for every point. The maximum score is 50, with the interpretation scoring (no disability = 0: 4, mild disability 5:14, moderate disability 15:24, severe disability 25: 34 and complete disability above 34

Time frame
four weeks
3

CROM

Cervical range of motion measured using CROM in different directions

Time frame
four weeks

Secondary outcomes

1

Visual analogue scale for pain (VAS-P)

is a method for measuring the intensity of pain on a horizontal straight line of fixed length (10 cm), as the left end of the line showed the greatest pain score \& the right end showed the least pain scores, then the patient was asked to put a mark, on the line according to his/her pain sensation, with a higher score representing the higher level of pain

Time frame
four weeks

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

October 6 University

Lead sponsor

Source ClinicalTrials.gov
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