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Clinical Trials/NCT02304120
NCT02304120
Completed
Not Applicable

Effects of a Sensorimotor Training on Postural Control and Pain: A Parallel, Single-blinded Randomised Controlled Trial

Michael A. McCaskey1 site in 1 country60 target enrollmentDecember 2014
ConditionsLow Back Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Low Back Pain
Sponsor
Michael A. McCaskey
Enrollment
60
Locations
1
Primary Endpoint
Change of self-reported pain on 100mm Visual Analogue Scale (VAS)
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

This study evaluates the effects of additional sensorimotor training (proprioceptive postural training, PPT) to conventional therapy in the treatment of chronic low-back pain. Half of the participants will receive instructed treadmill training as an active comparator against PPT. All participants receive conventional physiotherapy as prescribed by their treating medical doctors. It is expected that the PPT group will improve in postural control, proprioceptive, as well as pain and function outcomes to a significantly greater extent than the active control group.

Registry
clinicaltrials.gov
Start Date
December 2014
End Date
January 2016
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Michael A. McCaskey
Responsible Party
Sponsor Investigator
Principal Investigator

Michael A. McCaskey

Master of Science in Human Movement Science

Reha Rheinfelden

Eligibility Criteria

Inclusion Criteria

  • Patients with musculoskeletal low back pain (non-specific low back pain)
  • Age ≥ 18 years

Exclusion Criteria

  • Known or suspected neurological diseases or lesions
  • Traumatic injury of musculoskeletal system (fractures, tumours)
  • Spinal pathologies (e.g., tumour, infection, fracture, and inflammatory disease)
  • Previous spinal surgery
  • Presence of any contraindication to exercise (fracture or cardiovascular limitations)

Outcomes

Primary Outcomes

Change of self-reported pain on 100mm Visual Analogue Scale (VAS)

Time Frame: Baseline (-4 days); Pre-Test (0 days); Post-Test (+25 days) and follow-up (+45 days)

Change of functional status recorded with the Oswestry Disability Index (ODI)

Time Frame: Baseline (-4 days); Pre-Test (0 days); Post-Test (+25 days) and follow-up (+45 days)

Secondary Outcomes

  • Centre of Pressure(Baseline (-4 days); Pre-Test (0 days); Post-Test (+25 days) and follow-up (+45 days))
  • Joint Repositioning Error (segmental)(Baseline (-4 days); Pre-Test (0 days); Post-Test (+25 days) and follow-up (+45 days))
  • Uncontrolled Manifold Index (UCM)(Baseline (-4 days); Pre-Test (0 days); Post-Test (+25 days) and follow-up (+45 days))

Study Sites (1)

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