Randomized Single-Blind Clinical Trial in which the treatment will be administered through 3 sessions of dry needling in the cervical muscles's active trigger points in patients with chronic cervical pain.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
52
3 treatments of dry needling to inactivate all active trigger points found in patient's cervical muscles.
3 treatments of stretch applied to all cervical muscles that present active trigger points in patient's cervical muscles.
Centro Clínico de Fisioterapia OMT-E
Zaragoza, Spain
Cervical Pain Intensity
For the Assesment of cervical pain intensity the Numeric Pain Rating Scale (NPRS) was used.
Time frame: Change between baseline (immediately before intervention) and post intervention (immediately after intervention), after 1month and 3 months
Neck Disability Index
For the assesment of perceived neck disability the neck disability index was used.
Time frame: Change between baseline (immediately before intervention) and post intervention (immediately after intervention), after 1month and 3 months
Pressure Pain Threshold
For the assesment of pressure pain threshold of active trigger points a digital algometer was used
Time frame: Change between baseline (immediately before intervention) and post intervention (immediately after intervention), after 1month and 3 months
Cervical range of movement
For the assesment of cervical range of movement the universal goniometer was used
Time frame: Change between baseline (immediately before intervention) and post intervention (immediately after intervention), after 1month and 3 months
Cervical muscles Electromyography
For the assesment of cervical muscles electromyographic activity Trigno Avanti sensor was used.
Time frame: Change between baseline (immediately before intervention) and post intervention (immediately after intervention), after 1month and 3 months
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