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Clinical Trials/ISRCTN66262199
ISRCTN66262199
Completed
未知

Short-term effect on pain and function of neurophysiological education and sensorimotor retraining compared to usual physiotherapy in patients with chronic or recurrent non-specific low back pain (NSLBP): a randomized controlled trial

Zurich University of Applied Sciences (Switzerland)0 sites28 target enrollmentJanuary 8, 2014
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Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Zurich University of Applied Sciences (Switzerland)
Enrollment
28
Status
Completed
Last Updated
9 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
January 8, 2014
End Date
TBD
Last Updated
9 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Zurich University of Applied Sciences (Switzerland)

Eligibility Criteria

Inclusion Criteria

  • •1\. Men and women 18 to 60 years of age
  • •2\. A history of low back pain (LBP) of at least three months
  • •3\. Moderate disability, i.e. five points or more on the Roland and Morris Disability Questionnaire (RMDQ)
  • •4\. Medium or high risk for poor outcome, evaluated with the Keele Start Back Tool (KSBT)
  • •5\. Ability to speak and read German
  • •6\. Having someone available for assistance to execute home training
  • •7\. Having home access to the internet
  • •8\. Participants have to consent to an expenditure of time of 30 minutes five times per week over eight weeks to execute a home program and one to two 30\-minute physiotherapy sessions per week

Exclusion Criteria

  • •1\. Nerve root pain
  • •2\. Diagnosed specific spinal pathology (such as malignancy, fracture, infection or inflammatory joint or bone disease)
  • •3\. Pregnancy or less than 6 months postpartum
  • •4\. Coexisting major medical disease causing a relative or absolute contraindication to general exercise
  • •5\. Undergone spinal surgery within the preceding two years
  • •6\. Intra\-articular or perineural steroid injection on the lumbar spine during the previous five months

Outcomes

Primary Outcomes

Not specified

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