High Tone Power Therapy on Neck Pain and Proprioception in Cervical Radiculopathy
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: selected exercise program, High Tone Power Therapy.
- Who it may be relevant to
- Registry conditions: Cervical Radiculopathy. Basic parameters: 35 years — 50 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Egypt
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Effect of High Tone Power Therapy on Neck Pain and Proprioception in Cervical Radiculopathy Patients
Overview
To investigate the Effect of High Tone Power Therapy on Neck Pain and Proprioception in Cervical Radiculopathy Patients.
Detailed description
Forty two patients with Cervical Radiculopathy will participate in this study. The patients will randomly be divided into two equal groups; the control group which received the selected exercise program and the study group received the same exercise training program in addition to High Tone Power Therapy, three times per week for four weeks. The evaluation methods are cervical joint position error test, neck disability index, Cervical range of motion (CROM) and visual analogue scale
Interventions
- Other selected exercise program
therapeutic ultrasound, Static neck exercise - Device High Tone Power Therapy
High Tone Power Therapy delivered in cervical region 3 times per week for four weeks
Primary outcome measures
- cervical joint position error test [Time frame: four weeks]
- Neck disability index [Time frame: four weeks]
- CROM [Time frame: four weeks]
Secondary outcome measures (1)
- Visual analogue scale for pain (VAS-P) [Time frame: four weeks]
Eligibility criteria
Inclusion criteria
- 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.
- Cervical radiculopathy due to disc prolapse (C5-C6) (C6-C7) mild to moderate or disc prolapse according to magnetic resonance image (MRI).
- Normal body mass index (18.5 - 24.99Kg/m2).
Exclusion criteria
- 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.
- Structural abnormalities of the spine, osteoporosis, and spasmodic torticollis.
- Inflammatory or other specific disorders of spina such as ankylosing spondylitis and rheumatoid arthritis
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Egypt · 1 center
- October 6 university — Giza
Identifiers
NCT: NCT06695312 · P.T.REC/012/0053400