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Effect of dry needling in treatment of cervicogenic headache

Not Applicable
Recruiting
Conditions
cervicogenic headache.
Other headache syndromes
Registration Number
IRCT20181109041599N1
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
20
Inclusion Criteria

unilateral pain that radiating to the frontotemporal region
pain aggravated by neck movement and/or sustained awkward head positions
moderate to severe non throbbing pain
presence of active triggger points in the sternocleidomastoid muscle
Having reading and writing skills
headache frequency of at least 1 per week over a period greater than 3 months

Exclusion Criteria

cervical radiculopathy
a history of neck trauma;
trigger point therapy or trigger point dry needling in the neck within the previous 6 months
subjects > 65 y due to vascular defects
evidence of cognitive deficits
dry needling contraindication : needle phobia, pregnancy, ...
previously had surgery in the neck or shoulder area
a history of diagnosed primary headache
the presence of any tumor in the region
systemic disease: diabetes, anemia and ...

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Headache intensity. Timepoint: 2 weeks before and 2 weeks after intervention. Method of measurement: visual analogue scale.
Secondary Outcome Measures
NameTimeMethod
Headache frequency. Timepoint: 2 weeks before and 2 weeks after intervention. Method of measurement: days with headache.;Headache duration. Timepoint: 2 weeks before and 2 weeks after intervention. Method of measurement: hours with headache.;Headache disability index. Timepoint: 2 weeks before and 2 weeks after intervention. Method of measurement: Persian version of headache disability.
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