Radiculopathy, Cervical Clinical Trial
Official title:
Comparison of Spinal Mobilization With Arm Movement and Positional SNAGS on Pain and Disability in Cervical Radiculopathy Patients
Data will be collected in Hussain Memorial Hospital by taking informed consent. Randomised clinical trial is conducted taking thirty patients of both genders with confirmed diagnoses of cervical radiculopathy, their ages ranged from 25 to 60. A cluster of winner to rule out patient with cervical radiculopathy. They will be randomly assigned into two groups by the lottery method. Group A will receive conventional treatment and of spinal mobilization with arm movement (intervention 1) Group B will receive conventional treatment and positional SNAGs (intervention 2). The treatment will be conducted at a frequency of three sessions per week for four weeks. Two values will be taken, one as baseline and the other at end of the session. Then follow up the patient to rule out which intervention is more effective than the other. Neck Disability Index, Numeric Pain Rating Scale and ROM will be used to measure outcomes.
the objective of the study is To compare the effect of spinal mobilization with arm movement and positional SNAGs on pain and disability in cervical radiculopathy patients. The study design will be Randomized ClinicalTrial The sampling Technique will be Consecutive sampling technique Tool: The Neck Disability Index (NDI): used for measuring functional improvement in the neck. Numeric Pain Rating Scale (NPRS): used for measuring pain. Inclinometer: used for measuring Range of motion of cervical region. Data will be collected in Hussain Memorial Hospital by taking informed consent. Randomised clinical trial is conducted taking thirty patients of both genders with confirmed diagnoses of cervical radiculopathy, their ages ranged from 25 to 60. A cluster of winner criteria will be used to rule out patient with cervical radiculopathy. They will be randomly assigned into two groups by the lottery method. Group A will receive conventional treatment and of spinal mobilization with arm movement (intervention 1) Group B will receive conventional treatment and positional SNAGs (intervention 2). The treatment will be conducted at a frequency of three sessions per week for four weeks. Two values will be taken, one as baseline and the other at end of the session. Then follow up the patient to rule out which intervention is more effective than the other. Neck Disability Index, Numeric Pain Rating Scale and ROM will be used to measure outcomes. ;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Not yet recruiting |
NCT05971329 -
Pilot Study of ZetaFuse™ Bone Graft for the Treatment of Cervical Degenerative Disc Disease
|
Early Phase 1 | |
| Completed |
NCT00735176 -
The Norwegian Cervical Arthroplasty Trial
|
N/A | |
| Active, not recruiting |
NCT01911013 -
A Study of Korean Society of Spine Surgery on the Outcomes of Anterior Cervical Discectomy and Fusion
|
N/A | |
| Completed |
NCT04308122 -
Cervical Orthosis Versus no Orthosis Following Multi-level Posterior Cervical Fusion
|
N/A | |
| Active, not recruiting |
NCT03036007 -
Physiotherapy After Anterior Cervical Spine Surgery
|
N/A | |
| Recruiting |
NCT03023696 -
Can Prophylactic Foraminotomy Prevent C5 Palsy
|
N/A | |
| Terminated |
NCT02761928 -
Investigation of Hypermobility, Biomarkers, and Pain Generators in Chronic Pain Patients
|
||
| Recruiting |
NCT04623593 -
Cervical Arthroplasty Cost Effectiveness Study (CACES)
|
N/A | |
| Recruiting |
NCT06255444 -
Cervical Radiculopathy and Body Mass Index
|
||
| Not yet recruiting |
NCT03541681 -
Repeated Transforaminal Anesthetic Injections With or Without Glucocorticoid in Patients With Cervical Radiculopathy
|
N/A | |
| Completed |
NCT05082220 -
Analysis of Spread Level During Thoracic Erector Spinae Block
|
N/A | |
| Completed |
NCT00129714 -
Westeinde Brachialgia Study
|
N/A | |
| Completed |
NCT03890315 -
Evaluation of Neuropathic Pain in the Context of Clinical Symptoms, Quantitative Sensory Tests and Imaging With FMRI
|