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

U

Université du Québec à Trois-Rivières

Status

Completed

Conditions

Chronic Low Back Pain
Mechanical Low Back Pain

Treatments

Other: Biofeedback

Study type

Interventional

Funder types

Other

Identifiers

NCT02239289
FIR UQTR 2013-2014

Details and patient eligibility

About

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.

Enrollment

21 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

21 participants in 1 patient group

Biofeedback
Experimental group
Description:
Subjects will be provided with four sessions of supervised biofeedback training
Treatment:
Other: Biofeedback

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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