Cervicogenic Headache
Conditions
Brief summary
Patients suffering from Cervicogenic headache have restricted range of motion and pain which in turn causes functional disability and reduced quality of life. The aim of this research was to determine the effects of Graston technique to improve range of motion, function, and reduction of pain and in patients having Cervicogenic headache
Detailed description
A randomized controlled trial in which Graston Technique and Neuromuscular Re-education technique would be applied on patients presenting with cervicogenic headaches by using different tools and the changes would be examined pre and post intervention. The participants fulfilling inclusion criteria would be randomly allocated to two groups. Both groups received different protocols and will be assessed on data collection tool on their first and last visit using Goniometer, Headache Disability Index (HDI), Neck pain Disability Index (NDI) and Numeric Pain Rating Scale (NPRS). Participants of both groups will be pre-tested before the application of interventional techniques and post-tested after the application of respective intervention.
Interventions
DEVICEGarston tool
GT group protocol included the use application of IASTM along with the application of ice therapy at the end of the session. Using the Graston instrument, 20 strokes per minute proximal to distal and 20 strokes per minute distal to proximal for a period of 3 minutes were given over the painful area. Baseline values were recorded for demographics evaluation and episodes of pain onsets. The assessment of patients was done at the initial and last visit before the completion of the treatment program. Three treatment sessions per week were given to each patient for a total of four weeks.
PROCEDURENeuromuscular Re-education
General stretching and strengthening exercises for the neck muscles. The protocol of treatment for the NMR group included the use of the Neuromuscular re-education soft tissue mobilization technique (NMR) followed by active movements of the patient.
Sponsors
Health Education Research Foundation (HERF)
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
20 Years to 50 Years
Healthy volunteers
No
Inclusion criteria
* Age: Minimum 20years- Maximum 50 years (Male/Female) * Unilateral pain * Neck stiffness and ROM restrictions * Pain exacerbated by posture and neck movements * Pain effecting QOL * Positive flexion-rotation test
Exclusion criteria
* Headache not of cervical origin * Congenital condition of cervical spine * Headache with autonomic involvement, dizziness or visual impairment * Inability to tolerate the flexion rotation test * Conditions contraindicated for graston technique
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change from Baseline in pain on 10 points on Numeric Pain Rating Scale at 4th week | Baseline and 4th week | The Numeric Pain Rating Scale, is a validated, self reported tool assessing average pain intensity over period of last 24 hours. Possible pain ranges from 0( No pain) to 10 (Worst pain). Change= (Week 4 Score - Baseline Score ) |
| Change from Baseline in pain on 27 items on Headache Disability Index at 4th week | Baseline and 4th week | Headache Disability Index is a 27 items questionnaire that identify the limitations experienced due to headache. It includes questions to identify the frequency ranges from one per month, more than one but less than four per months, more than one per week and intensity of headache ranges from mild to moderate and to severe. |
| Change from Baseline in pain on 10 items on Neck Disability Index at 4th week | Baseline and 4th week | Neck Pain Disability Index is a 10 items questionnaire that identify the functional status of patients based on their conditions. it includes questions related to pain, personal care, reading, lifting, headaches, driving, sleeping , work, focus and leisure. |
Countries
Pakistan
Outcome results
None listed