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Effect of dry needling in treatment of cervicogenic headache

The effectiveness of one session dry needling of Sternocleidomastoid on pain and disability in patient with cervicogenic headache

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20181109041599N1
Enrollment
20
Registered
2019-05-04
Start date
2019-02-20
Completion date
Unknown
Last updated
2019-05-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cervicogenic headache. Other headache syndromes

Interventions

Intervention group: one session trigger point dry needling of Sternocleidomastoid muscle which is performed 10 times in the muscle..

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

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

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 ...

Design outcomes

Primary

MeasureTime frame
Headache intensity. Timepoint: 2 weeks before and 2 weeks after intervention. Method of measurement: visual analogue scale.

Secondary

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Mohammadi

Esfahan University of Medical Sciences

zahra.mohammadi_73@yahoo.com+98 31 3792 5000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 16, 2026