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The effect of dry needling on neck pai

Phase 3
Conditions
eck pain.
Segmental and somatic dysfunction of cervical region
M99.01
Registration Number
IRCT20160808029264N5
Lead Sponsor
Semnan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
30
Inclusion Criteria

Chronic neck pain more than 3 month
Presence of trigger point in the unilateral upper trapezius muscle
Neck disability index more than 10
Pain intensity between 3 and 6

Exclusion Criteria

Any neurogenic pain and radiculopathy, cardiovascular disorders, diabetes, hemophilia
Fibromyalgia syndrome
Any musculoskeletal disorders in the lower limbs
pregnancy
Needle phobia
Infection and edema in the treatment area
Consumption of anticoagulant drugs
Presence of trigger point in the other muscles of cervical and trunk regions

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Before, immediately and 10 days after the dry needling. Method of measurement: 100 mm visual pain scale.;Disabiity. Timepoint: Before, immediately and 10 days after the dry needling. Method of measurement: Disability questionnaire.;Range of motion. Timepoint: Before, immediately and 10 days after the dry needling. Method of measurement: Goniometer.
Secondary Outcome Measures
NameTimeMethod
Parameters of foot center of pressure. Timepoint: Before, immediately and 10 days after the dry needling. Method of measurement: Force plate.
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