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Comparison between Superficial and Deep Dry Needling on Surface Electromyography of Myofascial Trigger Point

Not Applicable
Recruiting
Conditions
upper trapezius myofascial trigger point.
Other disorders of muscle
Registration Number
IRCT20180918041059N1
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
50
Inclusion Criteria

Literate women 18 to 50 years
Unilateral neck or shoulder pain with at least one active Myofascial Trigger Point in the upper trapezius muscle for at least 3 months
Not receiving analgesic therapy by patients

Exclusion Criteria

Fear of dry needling
Local and systematic infection
People with fibromyalgia and neck osteoarthritis
People who used anticoagulant drugs
Acute muscle trauma
History of neck or shoulder surgery
History of receiving dry needling at last 6 months
Receiving physical therapy in the past month
Dry needling contraindications like pregnancy, allergy, existence of implants and pacemakers

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Surface electromyography activity. Timepoint: Before, immediately and one week after the intervention. Method of measurement: Surface electromyography device.
Secondary Outcome Measures
NameTimeMethod
eck disability. Timepoint: Before and one week after the intervention. Method of measurement: Neck disability index questionnaire.
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