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Effect of Cervical stabilization Exercises and Cervical Headache SNAG with Sensorimotor training On Pain And Functional Disability Among Cervicogenic Headache Patients

Phase 1/2
Not yet recruiting
Conditions
Acquired deformity of neck,
Registration Number
CTRI/2024/02/062923
Lead Sponsor
Shrushti Dixit
Brief Summary

Ethical clearance will be obtained from institutional ethical committee and principal of Dr. Ulhas Patil college of physiotherapy, jalgaon. A written informed consent form will be obtained from subject who are willing to participate. Subjects will be screened according to inclusion and exclusion criteria. The procedure, aim and objective will be explained to willing participants.Then participants screened with flexion-rotation test and to be confirmed with Cervicogenic headache. selected total 40 participants will be divided into two groups using simple random sampling or lottery method. All participants pre treatment evaluation NPRS, NDI, HDI score will be noted. Group’A’ will receive Cervical stabilization Exercises using pressure biofeedback unit along with sensorimotor retraining exercises which include oculomotor and postural stability exercises. And Group’B’ receive cervical headache SNAG along with sensorimotor retraining exercises. Both groups receive intervention for 5 weeks on alternate days. Post treatment response of all participants of NPRS, NDI, HDI will be noted

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria

Unilateral headache, headache with neck stiffness and pain, positive flexion-rotation test, restriction of extension and rotation range of motion in cervical spine, precipitation of headache with neck movement and sustained head positioning, intermittent headache of varying duration and pain level at the rate of one headache per week for greater than two months, headache with moderate intensity.

Exclusion Criteria

Chiropractic treatment in past 3 months, headache with autonomic involvement and visual disturbance, congenital condition of cervical spine, cervical radiculopathy, tension type headache and migraine, fracture or previous surgery on vertebral column, spinal stenosis and disc prolapse and TMJ dysfunction.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Numerical pain rating scale (NPRS), Neck disability index (NDI), Headache disability index (HDI)5 weeks , 3 days alternate in each week, total 15 sessions
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

DR ULHAS PATIL MEDICAL COLLEGE & HOSPITAL, JALGAON

🇮🇳

Jalgaon, MAHARASHTRA, India

DR ULHAS PATIL MEDICAL COLLEGE & HOSPITAL, JALGAON
🇮🇳Jalgaon, MAHARASHTRA, India
Dr Pradnya Mahajan
Principal investigator
9284034348
ppradz1816@gmail.com

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