About this trial
To investigate the neurophysiological relationship between Central Conduction Time measured via Somatosensory evoked potentials and pain intensity in individuals suffering from chronic neck pain
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Participants aged 18-35 years.
Normal Body Mass Index (BMI) less than 25 kg/m2.
Both genders were included.
having chronic neck pain lasting for more than three months.
Disqualifiers
signs of serious pathology (e.g., malignancy, inflammatory disorders, infection).
history of cervical spine surgery.
history of trauma or fractures in the cervical spine.
presence of vascular syndromes such as vertebrobasilar insufficiency.
Trial population
Participants aged 18-35 years, with normal Body Mass Index (BMI) of less than 25 kg/m2, including both genders were included.
Trial design
Other
Cross-sectional
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Chronic Neck Pain
Chronic Neck Pain measured using visual analogue scale
Secondary outcomes
Central Conduction Time
Central Conduction Time measured in milliseconds using Electromyography device (Neuro-EMG-Micro/4, Neurosoft, Russia)
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
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