Osteopathic Manipulative Treatment (OMT) on patients with Cervicogenic Headache Pragmatic randomized controlled clinical trial
- Conditions
- Secondary Headache DisordersC10.228.140.546
- Registration Number
- RBR-10yhrbnz
- Lead Sponsor
- Escola de Osteopatia de Madrid
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Age between 18 years and 49 years; Both sexes; Unilateral headache, starting in the posterosuperior region of the neck or occipital region, eventually spreading to the oculofrontotemporal on the symptomatic side; Pain triggered by neck movement and/or positions sustained inadequate; Reduced range of motion in the cervical spine; Pain caused by external pressure at at least one cervical level superior (C0 to C3/C4); Present moderate to severe complaint and/or symptoms, not throbbing and not lacinating; Headache frequency of at least once a week for a minimum period of 3 months; Have a minimum disability score of 20% or more (or that is, 10 points or more on the 0-50 NDI scale; Be able to move independently with or without the use of assistance; Be able to understand enough Portuguese to be able to fill in the questionnaires;
Other primary headaches Migraine, Tension Headache; Bilateral headaches; Time less than 6 months after surgery on the cervical spine, head or neck; history of cervical injury; upper limbs or region facial; Performing an invasive procedure for pain relief in the last 3 months; Receiving physical therapy, osteopathic or chiropractic treatment in the last 3 months; If you have two or more positive neurological signs consistent with nerve root compression muscle weakness involving a large upper extremity muscle group, decreased upper extremity deep tendon reflex, or decreased or absent pinprick sensation in any upper extremity dermatome; Diagnosis of cervical spinal stenosis; Exhibit these bilateral upper extremity symptoms; Evidence of central nervous system involvement hyperreflexia, sensory disturbances in the hand, hand atrophy, unsteadiness during gait, nystagmus, loss of visual acuity, decreased face sensation, taste alteration, presence of pathological reflex signs; Inflammatory rheumatic diseases eg rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis, systemic lupus erythematosus, etc.; Progressive neurological disease e.g. multiple sclerosis, Parkinson's disease, first neuron disease Unstable heart conditions;
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method