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Acupuncture in Neck Pai

Not Applicable
Conditions
Condition 1: Neck pain. Condition 2: Myofascial pain.
Cervicalgia
Injury of muscle, fascia and tendon at neck level
M54.2
Registration Number
IRCT20190104042229N1
Lead Sponsor
Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
45
Inclusion Criteria

Age between 18 to 35 years old
Having more than 12 weeks of history of Myofascial Neck Pain
Having pain above 3 is based on the VAS scale, which is considered as moderate pain
Satisfaction to participate in the research project Comparison of The Immediate Effects of Electroacupuncture and Laseracupuncture on Pain and Dysfunction Following Chronic Myofascial Neck Pain

Exclusion Criteria

History of Injection,Dry needling and Acupuncture In last month
History of Muscular Disease such as Fibromyalgia and myopathy
History of Neurological Disorders
Neck Discopathy and Radiculopathy
History of Neck Surgery
History of Negative response to Acupuncture or Dry needling
Needle Phobia
Malignancy and Patients susceptible to infection
Having vascular diseases and using anticoagulants
pregnancy
History of epilepsy or seizure
Diabetes
During menstruation

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The pain score of people based on the Visual Analog scale. Timepoint: Before the intervention, immediately after the intervention and one week after the intervention. Method of measurement: Visual Analog scale.;Pain pressure threshold. Timepoint: Before the intervention, immediately after the intervention and one week after the intervention. Method of measurement: pressure algometer.;Disability. Timepoint: Before the intervention, immediately after the intervention and one week after the intervention. Method of measurement: Neck Disability index Questionnaire.;Cervical range of motion. Timepoint: Before the intervention, immediately after the intervention and one week after the intervention. Method of measurement: Goniometer.
Secondary Outcome Measures
NameTimeMethod
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