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Clinical Trials/NCT03702075
NCT03702075
Unknown
Not Applicable

Effects of a Self-administered Program in Chronic Neck Pain Patients

Universidad de Granada1 site in 1 country50 target enrollmentSeptember 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Neck Pain
Sponsor
Universidad de Granada
Enrollment
50
Locations
1
Primary Endpoint
Trigger points examination
Last Updated
7 years ago

Overview

Brief Summary

Neck pain is a complex biopsychosocial disorder often precipitated or aggravated by neck movements or sustained neck postures. The onset and course of this pain are influenced by environmental and personal factors. Many studies report that participants preferred self-care measures for the management of neck pain and they sought professional help only when those measures fail.

Detailed Description

Neck pain is the fourth leading cause of disability worldwide causing an enormous impact on individuals and their families, communities and healthcare systems.While neck pain can be severely disabling and costly, treatment options have shown moderate evidence of effectiveness. No previous study has used foam roller in patients with neck pain. In addition, it has been suggested that neurodynamic interventions provide a peripheral stimulus, reducing the pressure existing within the nerve, improving blood flow, axonal transport and nerve conduction. It was hypothesized that a self-administered intervention focused on myofascial release of main muscles related to neck pain and upper-limb active neurodynamics could reduce the presence of active trigger points and pain, improving functionality and active mobility.

Registry
clinicaltrials.gov
Start Date
September 1, 2018
End Date
February 2019
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Marie Carmen Valenza

Principal investigator

Universidad de Granada

Eligibility Criteria

Inclusion Criteria

  • Chronic neck pain (at least 3 months' duration) not related to trauma of at least 3 on a visual analogue scale
  • Participants' symptoms had to be reproduced by median nerve upper-limb neurodynamic test.

Exclusion Criteria

  • Exclusion Criteria:
  • Whiplash related neck pain
  • Previous cervical surgical intervention
  • Cognitive impairments which prevent them to follow instructions
  • Visual or acoustic limitations
  • Physical therapy in the previous six months

Outcomes

Primary Outcomes

Trigger points examination

Time Frame: Change from baseline trigger points examination at 4 weeks

Trigger points will be explored bilaterally by a blinded assessor in suboccipital, scalene, levator scapulae and upper trapezius muscles

Secondary Outcomes

  • Pain severity(Change from baseline pain at 4 weeks)
  • Cervical range of motion(Change from baseline cervical range of motion at 4 weeks)
  • Functionality(Change from baseline functionality at 4 weeks)
  • Health related quality of life(Change from baseline health related quality of life at 4 weeks)
  • Fear avoidance beliefs(Change from baseline fear avoidance beliefs at 4 weeks)
  • Anxiety and depression(Change from baseline anxiety and depression at 4 weeks)

Study Sites (1)

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