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Effects of balance stimulation and cervical training on balance performance in chronic neck pai

Phase 2
Conditions
Chronic neck pain.
Biomechanical lesions, not elsewhere classified
Registration Number
IRCT2016060121459N2
Lead Sponsor
Vice Research of Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

inclusion criteria for patient group: complaint of neck pain for 3 months or more without referral to upper limb; age between 20 - 50;; no history of head and neck trauma; with a neck disability index score greater than 10%, VAS more than 3 ; neck pain at least twice during the last twelve months; not participation in exercise training during past 3 months. healthy subjects have not any musculoskeletal disorders. Exclusion criteria : Neurological disorders; cervical spine root compression; radiculopathy; preexisting vestibular pathology; connective tissue disease; cervical fracture and dislocation; Ankylosing spondylitis; mylopathy; cervical spine surgery; history of head and neck trauma, systemic disease; pregnancy; peripheral neuropathy; diabetes; inner ear disease; Rheumatic and inflammatory disease;fibromyalgia; respiratory / metabolic and cardiovascular disorders.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Mean excursion of COP. Timepoint: Before ,immediate after and 6weeks after intervention. Method of measurement: Force plate.;Maximum excursion of COP. Timepoint: Before ,immediate after and 6weeks after intervention. Method of measurement: Force plate.;Mean speed of COP. Timepoint: Before ,immediate after and 6weeks after intervention. Method of measurement: Force plate.;Rambling. Timepoint: Before ,immediate after and 6weeks after intervention. Method of measurement: Force plate.;Trembling. Timepoint: Before ,immediate after and 6weeks after intervention. Method of measurement: Force plate.;Frequency band of COP. Timepoint: Before ,immediate after and 6weeks after intervention. Method of measurement: Force plate.
Secondary Outcome Measures
NameTimeMethod
Pain intensity. Timepoint: Before, immediate after and 6 weeks after intervention. Method of measurement: VAS.;Pressure pain threshold. Timepoint: Before, immediate after and 6 weeks after intervention. Method of measurement: Algometer.;Joint position sense. Timepoint: Before, immediate after and 6 weeks after intervention. Method of measurement: Laser pointer and distance to reference point during cervical rotation and extension.;Neck disability level. Timepoint: Before and 6 weeks after intervention. Method of measurement: Neck disability Index.;Quality of life. Timepoint: Before and 6 weeks after intervention. Method of measurement: Short form12 questionnaire.
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