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Clinical Trials/NCT01402895
NCT01402895
Completed
Not Applicable

The Effect Of A Neurodynamic Treatment On Nerve Conduction In Clients With Low Back Pain

McMaster University1 site in 1 country9 target enrollmentMay 2011
ConditionsLow Back Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Low Back Pain
Sponsor
McMaster University
Enrollment
9
Locations
1
Primary Endpoint
Change in nerve conduction studies
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

The purpose of this study is to determine if a certain treatment for low back pain can change the way nerves in the leg send messages. Specifically, the investigators will examine whether a particular type of physical therapy treatment for individuals with low back pain (neurodynamic techniques) changes the speed that nerves send/receive signals to/from the leg, as compared to a different physical therapy treatment.

Registry
clinicaltrials.gov
Start Date
May 2011
End Date
October 2011
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Males and females aged 18 years and older
  • Participants who can speak English and read, understand, and fill out the consent form and questionnaires
  • Participants will have a certain level of low back pain graded numerically, with or without radiation to the leg
  • Clinical decision (by same individual) as safe to participate in study based on subjective history and objective examination.

Exclusion Criteria

  • An inability to tolerate sitting for 10 minutes
  • Nerve conduction disorders diagnosed by a physician such as, diabetes or MS
  • Current participant in an investigational drug study (within past 3 months)

Outcomes

Primary Outcomes

Change in nerve conduction studies

Time Frame: Change from baseline after intervention, on average 1.5 hours after baseline measure

Motor conduction of the tibial nerve; Sensory conduction of the sural nerve; H-reflex, H:M ratio (soleus muscle)

Secondary Outcomes

  • Change of knee extension in sitting slump test(Change from baseline after intervention, on average 1.5 hours after baseline measure)
  • Change in score of Visual Analog Scale for pain(Change from baseline after intervention, on average 1.5 hours after baseline measure)

Study Sites (1)

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