Skip to content

The effect of Pain Neurophysiology Education in the treatment of Cervicogenic headache

The effect of Pain Neurophysiology Education in the treatment of Cervicogenic headache: A randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200101045970N2
Enrollment
30
Registered
2020-09-30
Start date
2020-09-25
Completion date
Unknown
Last updated
2020-10-06

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

Conditions

Cervicogenic Headache. Other specified headache syndromes

Interventions

Intervention 1: Intervention group: Pain Neurophysiology Education: This method is taught to patients by the student. In the pain neurophysiology group, the training will be such that using simple met

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Unilateral headache that spreads to the frontotemporal region. Pain exacerbation associated with movement or inappropriate neck postures. Moderate to severe non-pulsatile pain based on Numeric Rating Pain Scale not lower than grade 2 Enough reading and writing skills are also a requirement for inclusion.

Exclusion criteria

Exclusion criteria: Neck Radiculopathy History of neck injury Any other neck pain agent, including osteoarthritis History of cervical trigger point treatment by manual or dry needle treatment over the past 6 months Cognitive disorders Previous history of primary headache diagnosis (such as migraine and tension headache) Use of painkillers during treatment Previous history of neck or shoulder surgery Failure to co-operate

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: Before and after treatment and one month follow up. Method of measurement: Visual Analog Scale.;Pain frequency. Timepoint: Before and after treatment and one month follow up. Method of measurement: Questionnaire.;Pain Duration. Timepoint: Before and after treatment and one month follow up. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Headache Disability Inventory. Timepoint: Before and after treatment and one month follow up. Method of measurement: Headache Disability Inventory.;Pain Catastrophizing rate. Timepoint: Before and after treatment and one month follow up. Method of measurement: Pain Catastrophizing Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Ehsan Ghasemi

Esfahan University of Medical Sciences

eghasemi@rehab.mui.ac.ir+98 31 3669 3089

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026