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Clinical Trials/NCT00929123
NCT00929123CompletedPhase 1

Mechanisms of Neural Mobilization in the Treatment of Chronic Pain

University of Florida1 site in 1 country40 target enrollmentStarted: May 1, 2007Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 1
Status
Completed
Enrollment
40
Locations
1
Primary Endpoint
thermal and pressure pain sensitivity

Study Overview

Brief Summary

The purpose of this study was to determine the effect of a manual therapy technique (neural mobilization) on measures of clinical pain and function, experimental pain sensitivity, and on the function of the median nerve in individuals with carpal tunnel syndrome. The investigators hypothesized that individuals receiving a neural mobilization technique known to directly stress the median nerve would demonstrate greater improvements in clinical pain and function, experimental pain sensitivity, and median nerve function than those receiving a sham technique.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •18 to 70 years of age
  • •signs and symptoms of carpal tunnel syndrome for greater than 12 weeks

Exclusion Criteria

  • •non english speaking
  • •prior surgery for carpal tunnel syndrome
  • •systemic condition known to affect sensation
  • •chronic pain condition other than carpal tunnel syndrome

Arms & Interventions

neural mobilization

Experimental

manual therapy technique known to directly stress the median nerve

Intervention: neural mobilization (Procedure)

sham neural mobilization

Placebo Comparator

manual therapy technique known to directly stress the median nerve without any stimulation.

Intervention: sham neural mobilization (Procedure)

Healthy Controls

Active Comparator

People without carpal tunnel syndrome for comparison

Intervention: healthy controls (Other)

Outcomes

Primary Outcomes

thermal and pressure pain sensitivity

Time Frame: immediate effect

Secondary Outcomes

  • wrist range of motion(3 weeks)
  • clinical pain(3 weeks)
  • median nerve function(3 weeks)
  • self report of disability(3 weeks)
  • grip strength(3 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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