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Clinical Trials/NCT03588364
NCT03588364CompletedNot Applicable

The Role of Osteopathic Manipulation in the the Management of Post-traumatic Migraine

University of California, San Diego2 sites in 1 country11 target enrollmentStarted: September 15, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
11
Locations
2
Primary Endpoint
Headache Frequency Log

Study Overview

Brief Summary

This study evaluates the use of osteopathic manipulation (manual medicine) for migraine headache following traumatic head injury. Headache is an important and very common somatic complaint among people with traumatic brain injury and an important cause of disability in the United States. Over 15-percent of soldiers deployed to Iraq sustained concussion. A majority of these patients suffer from headaches. Many of these are classified as migraine headache that do not respond to medications. Osteopathic manipulation is practiced by physicians in the United States and has been shown to be beneficial in some migraine patients. However, its use in the management of persistent post-traumatic headaches has not been explored. The investigators will use a randomized cross-over design to evaluate post-traumatic migraine patients' response to osteopathic manipulation.

Detailed Description

This is a 30-week prospective, randomized delayed treatment control group design in which 20 participants from the community will be randomized 1:1 into (a) an immediate treatment group that will receive 12 weeks of osteopathic manipulation (OMT) treatment plus standard of care right away or (b) delayed treatment group that will receive 12 weeks of OMT plus standard of care after a 6-week waiting period. The delayed treatment group initially serves as a control condition but then receives the experimental treatment. The investigators selected this control condition to improve our statistical power in this small pilot study. As noted, all participants will continue to receive standard of care throughout the study as a washout is not feasible with osteopathic manipulation and removing standard of care could exacerbate the participant's symptoms. Participants in both arms will be followed for another 12 weeks after the 12 weeks of OMT, resulting in 24 weeks of study participation for the immediate treatment group and 30 weeks of study participation for the delayed treatment group, with participants in both arms answering a series of questionnaires to evaluate migraine frequency and impact, treatment efficacy, side effects, adherence t standard of care and depressive symptoms every 6 weeks throughout their study participation. Participant encounters will consist of screening, psychometric and functional scale administration at every 6 weeks for a total of 24-30 weeks, as well as 12 weeks of OMT treatments for participants in both study arms. Study participants will likely come from UCSD internal referrals.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
Triple (Care Provider, Investigator, Outcomes Assessor)

Masking Description

Only the study coordinator and the participants are privy to the assigned treatment arm (immediate vs. delayed) until the study is complete and the database is locked.

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • History of TBI, concussion, post-concussive syndrome
  • Headache frequency >/equal 4 per month
  • Post-traumatic headache, migraine type
  • MIDAS Grade I-IV
  • Headaches continue to occur 3 months to 1 year after the injury
  • No history of uncontrolled migraine prior to head injury

Exclusion Criteria

  • Headache medication change (Tricyclic antidepressant, antiepileptic medication, propranolol, verapamil, duloxetine, butterbur, Botox) within 30 days
  • Non-pharmacologic headache management change (reduction in caffeine intake, reduction in alcohol intake, sleep hygiene, exercise) within 30 days
  • Less than 3 months from injury
  • History of uncontrolled migraine prior to TBI
  • Currently taking oral anti-coagulants

Arms & Interventions

Osteopathic Manipulation

Experimental

Twelve weekly sessions using the techniques of osteopathy in the cranial field.

Intervention: Osteopathic Manipulation (Other)

Waitlist Control

No Intervention

Six-week waiting period.

Outcomes

Primary Outcomes

Headache Frequency Log

Time Frame: 6 weeks

Participants will complete a form indicating the frequency, location, duration, characteristics, and associated features of their headache.

Secondary Outcomes

  • 36-Item Short Form Survey Instrument (MOS-SF-36)(6 weeks)
  • Migraine Disability Assessment Score (MIDAS)(6 weeks)
  • Center for Epidemiological Studies-Depression (CES-D)(6 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Hollis King

Health Sciences Clinical Professor

University of California, San Diego

Study Sites (2)

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