Bio-mechanical Reasoning and Lateral Specificity of Upper Cervical Joint Mobilization
Neck Pain
About this trial
This is an interventional treatment trial for Neck Pain focused on measuring neck stiffness, manual therapy, joint mobilization
Eligibility Criteria
Inclusion Criteria:
- males or females between 18 and 80 years of age
- 25 percent or greater asymmetry of active cervical range of motion rotation limited by pain and/or stiffness
Exclusion Criteria:
- cervical surgeries or injections in the past one year
- current manual or exercise treatment by another provider for neck pain
- cervical manipulation/mobilization/trauma in past 3 months
- cervical radicular or referred pain distal to the acromion
- upper extremity neurologic myotome weakness or constant dermatomal numbness
- pending litigation
- signs of cervical myelopathy or vertebrobasilar artery insufficiency
- use of prescribed anticoagulants or documented blood clotting disorder
- alar or transverse ligament instability
Sites / Locations
- Indiana University Health - West HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Bio-mechanically correct manual therapy (received first) arm
Bio-mechanically incorrect manual therapy (received first) arm
Participants will be randomized to receive manual therapy directed at the cervical spine atlanto-axial joints in the bio-mechanically correct direction followed by instruction in a home program to maintain this motion. Outcome measures will be assessed. Participants will return in 2-3 days and receive the opposite treatment and home program followed by outcomes assessment. Participants will return again in 2-3 days, outcomes will be assessed and the study will conclude. Participants will then be given the option to continue in formalized physical therapy if desired.
Participants will be randomized to receive manual therapy directed at the cervical spine atlanto-axial joints in the bio-mechanically incorrect direction followed by instruction in a home program to maintain this motion. Outcome measures will be assessed. Participants will return in 2-3 days and receive the opposite treatment and home program followed by outcomes assessment. Participants will return again in 2-3 days, outcomes will be assessed and the study will conclude. Participants will then be given the option to continue in formalized physical therapy if desired.