Mobilization With Movement vs. Neural Mobilization on Nerve Root Function in Patients With Cervic… (NCT05803954) | Clinical Trial Compass
CompletedNot Applicable
Mobilization With Movement vs. Neural Mobilization on Nerve Root Function in Patients With Cervical Radiculopathy
Egypt72 participantsStarted 2023-03-31
Plain-language summary
This study will be conducted to compare the effect of sustained natural apophyseal glides (SNAGS) versus neural mobilization on clinical outcomes such as 1- nerve root function in the form of: (A) peak to peak amplitude; (B) latency; (C) F wave. 2- pain pressure threshold (PPT) and 3- Neck disability index (NDI) in patients with cervical disc (C5-C6 and/or C6-C7) herniation.
Seventy two patients from both gender with cervical disc (C 5-C 6 and/or C 6- C7) herniation with both sensory and motor nerve affections will be recruited for this study following referral from an experienced neurologist and confirmed diagnosis by MRI. The patients' age will range between 20-50 years, body mass index (BMI) from 18 to 25 kg/cm2.
The patients will be assigned randomly by permuted block to three equal groups; group (A) will receive SNAGS in addition to traditional therapy, group (B) will receive neural mobilization in addition to traditional therapy and group (C) will receive traditional therapy.
peak to peak amplitude, nerve latency and F wave will be measured by electromyography, , pressure pain threshold will be measured by commander algometer. Neck disability will be measured by Arabic neck disability index.
Who can participate
Age range20 Years – 50 Years
SexALL
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Inclusion criteria
✓. seventy patients with cervical disc (C 5-C 6 and/or C 6- C7) herniation with both sensory and motor nerve affections, referred from neurologist and confirmed diagnosis by MRI
✓. Both sexes.
✓. Age between 20-50 years.
✓. Patients with neck pain radiating down to the arm.
✓. Patients with positive findings for spurling test, Upper Limb Tension Test One (ULTTO), cervical distraction test and cervical rotation test towards the symptomatic side \<60.
✓. BMI from 18 to 25 kg/cm2
✓. Existed active trigger points within middle trapezius and/ or cervical region.
✓. Positive Pittsburgh sleep quality index' value \>10, means moderate and/ or sever difficulty.
Exclusion criteria
✕. Patients experiencing primary shoulder or upper extremity problem of local origin
What they're measuring
1
F-wave parameters
Timeframe: Change over the course of the study, from baseline to the end of treatment program at 4 weeks
2
Somatosensory Evoked Potentials (SEPs) Latency and Amplitude
Timeframe: Change over the course of the study, from baseline to the end of treatment program at 4 weeks
3
Pain pressure threshold by Pressure algometer
Timeframe: Change over the course of the study, from baseline to the end of treatment program at 4 weeks