Assessing the effectiveness of a lateral glide cervical spine mobilisation on cervicobrachial (neck and arm) pai

Not Applicable

Completed

• Conditions: Musculoskeletal pain; Musculoskeletal Diseases; Other dorsopathies, not elsewhere classified

• Registration Number: ISRCTN62431186
• Lead Sponsor: niversity of Birmingham (UK)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2011-04-14
• Last Update Posted: 30 October 2017

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 96

Inclusion Criteria

1. Aged 18 - 65 years experiencing CBS (described as pain originating in the neck with associated pain radiating below the level of the shoulder joint into the arm) with or without parasthesia and or weakness in a dermatomal distribution
2. Had symptoms for greater than 6 weeks
3. Adequate knowledge of English to participate in a neuro-musculoskeletal examination and to answer the study questionnaire
4. Able to attend assessment and treatment appointments
5. Will have verbally agreed to attend the review appointment at 6, 26 and 52 weeks following initiation of the treatment

Exclusion Criteria

1. Presenting with any red flags: severe unremitting night pain, unexplained weight
loss, history of cancer, general malaise, and constant unvarying pain
2. Bilateral arm symptoms
3. Signs and symptoms strongly suggestive of thoracic outlet syndrome or a specificperipheral pathology e.g. adhesive capsulitis, sub acromial impingement etc.
4. Specific pathology affecting nerve function e.g. multiple sclerosis, known peripheral vascular disease, diabetes
5. Known specific pathology affecting systemic joint function e.g. rheumatoid arthritis, ankylosing spondylitis
6. Cervical spine surgery, botulinum toxin injections or epidural injections to cervical spine or planned imminent treatment
7. Having other forms of manual therapy for their CBS symptoms e.g. osteopathy or chiropractics
8. Involved in compensation and or litigation associated with neck and or upper limb pain
9. Already involved in a research trial

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain, assessed by Visual Analogue Score (VAS)

Secondary Outcome Measures

Name	Time	Method
1. Short Form 36-item Health Survey (SF36) (RAND)<br>2. Neck and Upper Limb Index (NULI) <br>3. Tampra scale of Kinesiophobia<br>4. Global Rating of Change (GROC)<br>5. Self-Administered Leeds Assessment of Neuropathic Symptoms and Signs (S-LANSS)<br>6. Upper limb nerve extensability test<br>7. Cervical Active Range Of Motion (AROM)