Health Condition 1: M959- Acquired deformity of musculoskeletal system, unspecified
Conditions
Interventions
Intervention1: Group 1- Sensorimotor Training along with conventional exercise: Patient will perform cervical joint position sense training with lesser pointer and oculomotor control exercises (i.e ey
Sponsors
Avrajir Sarkar
Eligibility
Inclusion criteria
Inclusion criteria: Subjects diagnosed with cervicogenic headache according to established diagnostic criteria, third edition of the International Classification of Headache Disorders (ICHD-3). The ICHD-3 criteria for cervicogenic headache are as follows: 1. Any headache fulfilling criterion C 2. Clinical and/or imaging evidence of a lesion or disorder in the cervical spine or soft tissues of the neck that can cause headache 3. Evidence of cause of headache demonstrated by at least two of these: 3.1 Headache has developed in temporal relation to the appearance of the lesion or the onset of the cervical disorder 3.2 Headache has significantly improved or resolved in unison with improvement in or the resolution of the cervical lesion or disorder 3.3 Cervical range of motion is reduced, and provocative maneuvers may significantly worsen the headache 3.4 Headache is abolished following diagnostic blockade of a cervical structure or its nerve supply 4. Not better accounted for by another ICHD-3 diagnosis. History of neck pain occurring for more than three months and joint position error of more than 3 in at least two out of four directions of neck movements (flexion, extension, left and right rotation)
Exclusion criteria
Exclusion criteria: 1. Tension-type headaches and migraine 2. Internal carotid or vertebral artery dissection 3. Arnold-Chiari malformation 4. Herniated intervertebral disc 5. Intramedullary or extramedullary spinal tumor 6. Spinal nerve compression or tumor 7. Arteriovenous malformation 8. Neck-tongue syndrome
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Headache disability inventory, Cervical joint position errorTimepoint: the data will be collected at baseline and after intervention given for a time period of 4 weeks. | — |
Secondary
| Measure | Time frame |
|---|---|
| craniocervical enduranceTimepoint: the data will be collected at baseline & after intervention given for a time period of 4 weeks. | — |
Countries
India
Contacts
Public ContactAvrajit Sarkar
SGT University
Outcome results
None listed