The Effect of Osteopathic Treatment on Craniocervico-Mandibular Dysfunction

🩺 Protocol Summary

The goal of this clinical trial is to measure the effects of osteopathic manipulative treatment (OMT) on tissues of the craniocervico-mandibular unit (CCMU) in individuals with neck pain and headaches. The main questions to answer are: 1. How does OMT affect CCMU muscle stiffness 2. How does OMT affect jaw motion 3. How does OMT affect autonomic function 4. Is pain pressure threshold affected by OMT of the CCMU Participants will undergo the following interventions: 1. Photos taken to measure head and neck angles 2. Ultrasound 3. Smooth Pursuit Neck Torsion Test 4. Motion Capture 5. Autonomic Protocol 6. Algometry 7. Surveys

Primary Research Facility: Edward Via College of Osteopathic Medicine-Auburn (Auburn, Alabama)

Review these 3 basic logistical and protocol criteria extracted from the public NIH record. (This is a preliminary logistical checklist, not an official clinical eligibility determination).

Diagnosed with, undergoing evaluation for, or seeking treatment related to Headache?

🔍 Study Population / Focus Area (Source: Protocol Primary Condition)

Aged between 19 Years and 65 Years?

🔍 Protocol Specified Age Range: 19 Years to 65 Years

Able to attend required clinic visits at Edward Via College of Osteopathic Medicine-Auburn (Auburn, Alabama)?

🔍 Logistical Requirement: Site at Edward Via College of Osteopathic Medicine-Auburn

📍 Primary Site Map

Site: Edward Via College of Osteopathic Medicine-Auburn — Auburn, Alabama

💰 Clinical Trial Costs & Insurance Coverage

Coverage for clinical trial participation varies depending on your health insurance policy, state legislation, and whether specific procedures are investigational research or routine medical care. Under federal law (Affordable Care Act § 2709), health insurers generally cannot drop coverage or refuse to pay for routine patient care costs incurred in approved clinical trials.

💡 Always ask the study coordinator for the trial's official Informed Consent Form, which outlines all sponsor-funded research items versus procedures billed to your insurance.