All participants
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Inclusion criteria: Male and female, Age 18 – 70 years,
Able and willing to participate, No large radiological
investigations or treatments in the past two years (effective
dose > 10 mSv), Capable of giving informed
consent, Not pregnant or likely to be pregnant, Willing for general
practitioner to be informed about participation.
|
Exclusion criteria: History of cervical spine surgery, Poor
understanding of English, Current involvement as a subject in
another research study.
|
Patients
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Inclusion criteria: Mechanical neck pain (reproducible by neck
movement/provocation tests) and no identifiable aetiology e.g.
infection, inflammatory disease, Pain located within the area
defined by the Neck Pain Task Force, Self-reported pain rating 3 or
more on a 11-point numerical rating scale, Pain of at least
2 weeks duration, No contraindications to spinal manipulative
therapy.
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Exclusion criteria: Non-mechanical neck pain, Depression history,
Litigation/compensation pending, Manual therapy already received
for this episode of neck pain, Primary complaint of arm pain,
Traumatic onset of this neck pain episode, Central hypersensitivity
as assessed by pressure algometry.
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Healthy volunteers |
Inclusion criteria: No activity-limiting neck pain lasting more
than 24 hours in the last 12 months, No current neck
pain, dizziness or vertigo (unsteadiness).
|
Exclusion criteria: Cervical/thoracic spine manipulation in week
prior to baseline imaging. |