Migraine Clinical Trial
— OMTHAOfficial title:
Physiological and Behavioral Effects of Osteopathic Manipulative Treatment on Patients With Chronic Headache: A Randomized Clinical Trial
Participants with chronic or recurrent headache, unrelated to any known pathology or disease, will be randomly assigned to one of four interventions: Osteopathic manipulation of the body other than the head, osteopathic manipulation of the head, osteopathic manipulation of the head and rest of the body, or light touch on the head only but no manipulation. Measurements of heart rate and blood pressure variability, peripheral blood flow, and behavioral changes, such as mood, pain duration, intensity and frequency will be assessed.
Status | Completed |
Enrollment | 60 |
Est. completion date | December 2012 |
Est. primary completion date | December 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - chronic or recurrent headaches at least as often as one time per week Exclusion Criteria: - recent head trauma - brain disease or pathology - seizure disorder - using beta or alpha blocker medications - allergy to sticky tape used to affix leads to skin |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | Western University of Health Sciences | Pomona | California |
Lead Sponsor | Collaborator |
---|---|
Western University of Health Sciences |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Head pain frequency | seven days after the intervention participants will be called by telephone and asked whether they had their usual headache in the week following the intervention. | one week after intervention | No |
Secondary | Head pain intensity | one week after intervention participants will be contacted and asked to rate the intensity of their headaches after the intervention. | one week | No |
Secondary | Head pain duration | one week after the intervention participants will be contacted and asked the duration of the headaches. | one week | No |
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