About this trial
the goal of this clinical trial is to study the Impact of adding integrated neuromuscular inhibition technique to cervical stabilization exercise in chronic mechanical neck pain
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age from 18-44 year
Their body mass index will be ranging from (18-25) Kg/m2
All patient has active cervical trigger point of the upper fiber of the Trapezius detected by pincer palpation
Subjects must have characteristics of trigger points hardened, thickened taut bands in MPS patients.
Disqualifiers
Individuals with a recent history of neck or back surgery.
Individuals with recent history of trauma or fracture.
Individuals with congenital and pathological disorders of the cervical spine.
Individuals with any psychiatric diseases
Trial design
Parallel
Treatments tested in this trial
Cervical stabilization exercise and Integrated Neuromuscular Inhibition
Devicecervical stablization exercise starting with cervical isometric exercises performed in the supine position. The head will be supported on a pillow with a towel roll placed under the cervical spine to ensure proper alignment. Additional cervical isometric exercises will be conducted in the seated position by applying manual resistance at the forehead to perform cervical flexion, extension, rotation, and side-bending movements. The Integrated Neuromuscular Inhibition will be applied to the upper trapezius muscle to deactivate myofascial trigger points and reduce muscle tension. The technique will consist of three sequential components: intermittent ischemic compression, strain counterstain, and muscle energy technique
Integrated neuromuscular inhibition technique
DeviceIntegrated Neuromuscular Inhibition will be applied to the upper trapezius muscle to deactivate myofascial trigger points and reduce muscle tension. The technique will consist of three sequential components: intermittent ischemic compression, strain counterstain, and muscle energy technique
Conventional Treatment group
Other interventionParticipants in this group will receive conventional physical therapy only in the form of superficial heat using hot pack for 10 minutes, stretching exercise, isometric neck exercise and posture advice for 3 sessions/week over 4 weeks' periods.
Treatment groups
Trial outcomes
Primary outcomes
Pain threshold
Measured by using Pressure algometer
Secondary outcomes
pain intensity
Measured by using Visual Analog Scale
Range of Motion
Measured by using mobile application clinometer
Neck function
Measured by using neck disability index
Neck proprioception
Measured by using mobile application clinometer
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: