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Use of Biofeedback Training to Correct Abnormal Neuromechanical Pattern in Chronic Low Back Pain Patients

CompletedNot applicableNCT02239289
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

Brief summary (from the registry)

The purpose of the present study is to evaluate the benefit of biofeedback training on the capacity of chronic low back pain patients to decrease their lumbar paraspinal muscles activity during trunk full flexion and its relationship with changes in clinical outcomes. To do so, twenty patients with nonspecific mechanical low back pain will be recruited and all participants will take part in four sessions of supervised biofeedback training, consisting of 5 blocks with at least 12 trunk flexion-extension tasks. It is hypothesized that participants will have improved neuromechanical parameters with the biofeedback training and that this improvement will be positively associated to changes in clinical outcomes. This study will also allow for generation of preliminary data, in order to plan for a larger randomized control trial.

Study details

Official title
Correction of Abnormal Flexion-relaxation Phenomenon in Chronic Low Back Pain: the Benefit Associated With Biofeedback Training
Interventions
  • Other: Biofeedback
Sponsor
Université du Québec à Trois-Rivières
Start date
2014-03
Primary completion
2014-09
Sex
All
Age range
from 18 Years to 60 Years
Results posted
Yes, on ClinicalTrials.gov
Countries
Canada
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Being between 18 and 60 years of age. * Presence of non-specific chronic low back pain. Exclusion Criteria: * Prior surgery or major spine trauma. * Lumbar scoliosis greater than 20°. * Neuromuscular disease. * Malignant tumor. * Uncontrolled hypertension. * Infection. * Neurological deficit. * Symptomatic lumbar disc herniation. * Pregnancy. * Recent lumbar cortisone injection. * Active lower body injury and/or disabling pain limiting the capacity to complete the experimentation. * Being under medications known to impair physical effort and pain perception.

Canadian sites (1)

FacilityCityProvince
Université du Québec à Trois-RivièresTrois-RivièresQuebec

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT02239289