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The Effects of Thoracic Spine Mobilizations in Individuals With Neck Pain.

Not Applicable
Conditions
Neck Pain
Registration Number
NCT02356380
Lead Sponsor
Chatham University
Brief Summary

To determine the affects of Physical Therapists clinical reasoning using thoracic spine mobilization for neck pain compared to a standard protocol.

Detailed Description

The purpose of this research is to compare the effects of two commonly used, safe, thoracic spine treatments: grade 1-4 as performed by Cleland et. al. and grade 1-4 mobilization to the thoracic spine as selected by the Physical Therapist for cervical spine pain. The immediate effects of thoracic spine mobilization have been shown to facilitate greater range of motion increases in the cervical spine and greater pain decreases within a treatment session and on follow-up visits. There is no research utilizing pain threshold perception as an objective outcome of these treatments. Only one study compared the two treatment techniques and concluded that future research should be completed which includes manual therapy for the thoracic spine. (Cleland 2007) If the PT identifies an appropriate patient they will ask if they are interested in being a research subject. The Physical Theapist recruiting subjects all have completed their Doctor of Physical Therapy Degree and have advanced training in manual Physical Therapy. The techniques employed are considered standard practice and are defined as entry level skills by the Comission of Accredicdation of Physical Therapy Programs. These techniques are typically taught in DPT degree programs.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Patients with Neck Pain
  • Ages 18 - 60
Exclusion Criteria
  • Red flags: leg weakness, night pain, history of cancer, upper motor neuron signs, infection, tumors, osteoporosis, fracture (Boissonnault, 2011) (Cleland, 2004), cervical stenosis, CNS involvement, signs consistent with nerve root compression, previous surgery, pending legal action

The inclusion and exclusion above represent a conservative approach based on combining criteria of recent studies in published review articles. (Cross, 2011; Walser, 2009

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Neck Disability Index2 weeks

Assessment of function of neck using a valid and reliable written tool.

Global Rating of Change2 weeks

A written scale assessing overall improvement

Neck Pain2 weeks

0-10 scale

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Chatham University

🇺🇸

Pittsburgh, Pennsylvania, United States

Chatham University
🇺🇸Pittsburgh, Pennsylvania, United States
Steve A Karas, DSc
Principal Investigator

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