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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03015493
Other study ID # CHR7
Secondary ID
Status Active, not recruiting
Phase N/A
First received January 6, 2017
Last updated January 13, 2017
Start date May 2016
Est. completion date February 2017

Study information

Verified date January 2017
Source European University Cyprus
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to examine the effects of cervical traction with or without the addition of neural mobilization, in patients with cervical radiculopathy


Description:

Background:Cervical radiculopathy (CR) is a disorder of the peripheral nervous system where the resulted cervical nerve root (CNR) pathology produces a chronic pain and disability. Based on some epidemiological findings, CR is a common clinical diagnosis since its annual incidence has been estimated to be 83 cases per 100,000, with an increased prevalence noted in the fifth decade of life. In addition, C6 and C7 nerve roots are most commonly involved in this disorder, mainly due to the high range of motion occurring between cervical vertebrae C5-C6 and C6-C7.

CR is caused by a disc herniation, or a space-occupying lesion that can result in CNR inflammation, impingement, or both. In normal situations, CNRs ensure the normal function of sensation, movement and motor coordination of the upper limb. Therefore, the development of CR can produce sensory and motor deficits in the involved limb, including pins and needles, numbness and muscle weakness, along with a neuropathic pain described as a burning or shooting pain. These symptoms lead patients to exhibit severe functional limitations such as difficulties to work, to sleep or to participate in hobbies. Studies on this topic identified several socioeconomic and psychological deficits, from lost work and wages to prolonged pain and impaired social functioning, leading patients with CR to express symptoms of anxiety and depression.

Treatment of CR has been the subject of debate between physiotherapists and researchers. Several non-operative treatment approaches have been advocated to reduce CR pain and their analgesic effect has been recognized in a number of randomized clinical trials with these in turn being analyzed in few systematic reviews. Based on these studies, patients with CR can benefit from a multimodal treatment approach including the application of postural education, cervical traction and manual therapy techniques (mobilization, thrust manipulation etc.) applied to the cervical spine. However the small number of these studies as well as their poor methodological quality due to the short-term follow ups, lack of patient's homogeneity, randomization or control group etc., raise several questions about the validity of research findings and therefore much more studies are necessary. Among manual therapy techniques that have been recommended to improve the patient's pain and functional limitations, neural mobilization (NM) has been advocated as an effective treatment option. NM introduced as an intervention for pain relief more than 25 years ago are techniques that involve a specific sequence of joint movements to mobilize the involved peripheral nerve in order to facilitate the reduced nerve gliding and reduced the increased neural mechanosensitivity.

The application of NM is common but since now little research attention has been given to support its usage in patients with CR. Recently, a case study and a randomized controlled study concluded that neural mobilization applied simultaneously with cervical traction can produce clinically meaningful improvements over a 4-week period, in terms of pain, disability, function, grip strength and cervical spine range of motion. However, both methodological designs did not allow determining whether NM provided these benefits. Thus, the purpose of the present study was to examine the effects of cervical traction with or without the addition of NM, in patients with CR.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 50
Est. completion date February 2017
Est. primary completion date February 2017
Accepts healthy volunteers No
Gender All
Age group 22 Years to 71 Years
Eligibility Inclusion Criteria:

- Unilateral sensory and motor deficits including sharp pain, muscle weakness and numbness in the upper arm

- A positive result in a minimum three of four tests (Spurling's test, Distraction test, Upper Limb Neurodynamic Test 1 and ipsilateral cervical rotation of less than 60) of a clinical prediction rule. This clinical prediction rule has demonstrated 94% specificity (95% = 0.88 to 1.00), 24% sensitivity (95% = 0.05 to 0.43) and a positive likelihood ratio of 6.1 (95% = 2.0 to 18.6) when 3 of 4 items were positive

Exclusion Criteria:

- A current history of cervical myelopathy or signs of upper motor neuron disease

- Bilateral CR or other musculoskeletal conditions in the affected limb.

- Receive of any prescription or over-the-counter analgesia or anti-inflammatory medication during the prior two weeks

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Neural mobilization combined with traction
Neural mobilization techniques combined with cervical traction for the cervical nerve roots
Traction
Traction techniques for the cervical spine

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Christos Savva

References & Publications (1)

Young IA, Michener LA, Cleland JA, Aguilera AJ, Snyder AR. Manual therapy, exercise, and traction for patients with cervical radiculopathy: a randomized clinical trial. Phys Ther. 2009 Jul;89(7):632-42. doi: 10.2522/ptj.20080283. Erratum in: Phys Ther. 20 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Neck Disability Index Change from baseline after 4 weeks
Secondary Numeric Pain Rating Scale Change from baseline after 4 weeks
Secondary Patient-Specific Functional Scale Change from baseline after 4 weeks
Secondary Grip strength measurement using a dynamometer Change from baseline after 4 weeks
Secondary Measurement of cervical spine active range of motion using a universal goniometer Change from baseline after 4 weeks
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