About this trial
Cervical radiculopathy is a condition of cervical spinal nerve roots which occurs as a result of compression and inflammatory pathology from a space occupying lesion. Nerve flossing technique is a quick mobilization of the strained nerves which will reduce pain .This study aim to determine the effects of nerve flossing technique on pain, range of motion and disability in patients with cervical radiculopathy.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Participants with 30 to 50 years of age group were taken in this study (Gore et al., 2020)
Patients with positive Spurling test ,cervical distraction ,cervical rotation test were included
Participants with positive Upper limb neural tension test for median nerve were taken into consideration
Patients who are having radicular symptoms and pain for more than 3 months were included
Disqualifiers
Systematic disorders affecting musculoskeletal disorders e.g. Ankylosing spondylitis,rheumatic arthritis etc.
Patient with primary shoulder or upper limb pain origin
Patients with severe malignancy,COPD ,isch
Trial design
Parallel
Treatments tested in this trial
Median nerve flossing technique and conventional physical therapy
Other interventionMedian nerve flossing technique and conventional physical therapy Nerve flossing will be started from root along brachial plexus,median nerve root. Before starting the procedure ,subjects will be shown the flossing technique as it will be performed actively by the subjects. Each flossing will be performed with 10 repetitions starting from neck,arm,elbow,wrist and whole nerve flossing (12). It will be a 3 week treatment with 4 session per week (12 sessions)
Conventional physical therapy
Other interventionThe subjects in this group will be treated with TENS and hot pack. All the subjects will be screened according to the inclusion and exclusion criteria .Written informed consent will be taken from all the subjects before the treatment. The subjects will be allowed to withdraw the treatment any time.The subjects will be divided into 2 groups through convenience sampling.All the subjects from both group will be given trancutaneous electric nerve stimulation TENS ,hot pack, isometrics and stretching as a conventional physical therapy followed by respective group techniques The session will last for 20 -25 minutes , TENS pad will be placed in the suboccipital region and the trapezius unilaterally with hot pack simultaneously for 10 minutes
Treatment groups
Trial outcomes
Primary outcomes
numeric pain rating scale
The intensity of pain was assessed with the help of NPRS. The scale have readings that numerate from 0 to 10,beginning with least reading 0 that indicates no pain ,5 indicates moderate level of pain and 10 indicates extreme level of pain.Test-retest reliability of NPRS was high
Secondary outcomes
goniometer
Universal goniometer was used to measure range of motion of cervical region that has an inter-rater reliability
Other outcomes
universal goniometer
Disability level of neck was demonstrated by using Neck Disability Index (NDI) questionnaire .It consist of total 10 sections, each with 0-5 rating scale in which 0 indicates "
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: