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Clinical Trials/NCT02660801
NCT02660801
Terminated
Not Applicable

Spinal Manipulation and Spinal Mobilization Effects in Participants With and Without Back Pain

Université du Québec à Trois-Rivières1 site in 1 country26 target enrollmentMarch 2016
ConditionsBack Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Back Pain
Sponsor
Université du Québec à Trois-Rivières
Enrollment
26
Locations
1
Primary Endpoint
Muscular Response, Inferior Level Ratio, Normalized RMS
Status
Terminated
Last Updated
6 years ago

Overview

Brief Summary

The objective of the present study is to compare the neuromechanical responses to spinal manipulation and spinal mobilization in participants with chronic nonspecific middle back pain.

Detailed Description

Although evidences suggest a similar effectiveness of spinal manipulation and spinal mobilization, there is no study that compares the neuromechanical effects of these manual therapies in a experimental context and with the standardization of both interventions. Therefore, the objective of the present study is to compare the neuromechanical responses to spinal manipulation (low-amplitude and high-velocity dynamic thrust) and spinal mobilization (repetitions of a low-amplitude and low-velocity nonthrust movement) in participants with and without chronic nonspecific back pain.

Registry
clinicaltrials.gov
Start Date
March 2016
End Date
November 2017
Last Updated
6 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Martin Descarreaux

Dr Martin Descarreaux DC, PhD

Université du Québec à Trois-Rivières

Eligibility Criteria

Inclusion Criteria

  • presenting or not a history of chronic nonspecific back pain

Exclusion Criteria

  • History of back trauma or surgery
  • Severe osteoarthritis
  • Inflammatory arthritis
  • Vascular conditions
  • Contraindication to the use of spinal manipulation or spinal mobilization
  • Pregnancy
  • Scoliosis

Outcomes

Primary Outcomes

Muscular Response, Inferior Level Ratio, Normalized RMS

Time Frame: During the spinal manipulation and mobilization

To assess the muscular response during therapeutic modalities, the resulting bipolar sEMG signals were first digitally band-pass filtered using a frequency bandwidth of 20-450 Hz (2nd order Butterworth filter). For SMa, the peak root mean square (RMS) value was computed for each electrode using a 250 ms window (125 ms before and 125 ms after the peak force). The RMS values obtained for each electrode were then normalized (nRMS) to the respective RMS value calculated during the sEMG normalization trial.

Terminal Spinal Stiffness

Time Frame: two-minutes before spinal mobilization delivery up to two-minutes after

Terminal stiffness was defined as the ratio of the variation of force and displacement between 10 and 45 N

Pressure Provoked Pain

Time Frame: immediately after the therapeutic modality application

Pressure provoked pain intensity was assessed immediately after each spinal stiffness assessment using a 0 to 100 visual analog pain scale minimum value=0, maximum value=100. 0 is no pain while 100 is the worse outcome

Global Spinal Stiffness

Time Frame: two-minutes before spinal manipulation delivery up to two-minutes after

Global stiffness was defined as the slope of the straight-line best fitting the force-displacement data between 10 and 45 N

Muscular Response, Superior Level Ratio

Time Frame: During the spinal manipulation and mobilization

To assess the muscular response during therapeutic modalities, the resulting bipolar sEMG signals were first digitally band-pass filtered using a frequency bandwidth of 20-450 Hz (2nd order Butterworth filter). For SMa, the peak root mean square (RMS) value was computed for each electrode using a 250 ms window (125 ms before and 125 ms after the peak force). The RMS values obtained for each electrode were then normalized (nRMS) to the respective RMS value calculated during the sEMG normalization trial.

Study Sites (1)

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