Effects of Lumbar Repositioning Feedback and Transversus Abdominis Training on Lumbar Propricption in Patients With Chronic Mechanical Low Back Pain

Sponsor
October 6 University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05047614
Collaborator
(none)
48
1
4
27.9
1.7

Study Details

Study Description

Brief Summary

This study is conducted to answer the following question: What is the effect of lumbar repositioning feedback and transverses abdominis training on lumbar proprioception in patients with chronic mechanical low back pain?

Condition or Disease Intervention/Treatment Phase
  • Device: including sham
N/A

Detailed Description

Chronic low back pain is a chronic pain syndrome in the lower back region, lasting for at least twelve weeks. Chronic low back pain represents the leading cause of disability worldwide and is a major welfare and economic problem. Low back pain represents a major social and economic problem. The prevalence of chronic low back pain is estimated to range from fifteen to forty-five percent in French healthcare workers. Low back pain symptoms can derive from many potential anatomic sources, such as nerve roots, muscle, fascial structures, bones, joints, intervertebral discs, and organs within the abdominal cavity. Moreover, symptoms can also spawn from aberrant neurological pain processing causing neuropathic low back pain. Low back pain has been associated with motor control dysfunction. Indicators of this dysfunction include decreased contraction of the transversus abdominis and multifidus muscles, the reduced cross-sectional area of the multifidus, and fat infiltration. An association of chronic low back pain with altered muscle recruitment patterns and transversus abdominis activation delay was also found, as well as increased back muscle fatigue and altered kinematic patterns in the hips and lumbar area.

This was further supported in two recent systematic reviews that reported that proprioception deficits were found in patients with chronic low back pain compared to healthy controls

Study Design

Study Type:
Interventional
Anticipated Enrollment :
48 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Effects of Lumbar Repositioning Feedback and Transversus Abdominis Training on Lumbar Propricption in Patients With Chronic Mechanical Low Back Pain
Actual Study Start Date :
Apr 19, 2020
Anticipated Primary Completion Date :
May 2, 2022
Anticipated Study Completion Date :
Aug 15, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Study 1

Twelve patients in study group 1 receiving lumbar repositioning feedback training

Device: including sham
Repositiong feedback training and biofeedback pressure training unit

Experimental: Study 2

Twelve patients in study group 2 receiving transverses abdominis training

Device: including sham
Repositiong feedback training and biofeedback pressure training unit

Experimental: Study 3

Twelve patients in study group 3 receiving both lumbar repositioning feedback training and tranversus abdominis training

Device: including sham
Repositiong feedback training and biofeedback pressure training unit

Experimental: Control

Twelve patients in control group receiving conventional lumbar propriception physical therapy program .

Device: including sham
Repositiong feedback training and biofeedback pressure training unit

Outcome Measures

Primary Outcome Measures

  1. Pressure biofeedback unit [up to 45 days]

    Assessment of transversus abdominis activation

  2. feedback laser tracker [up to 45 days]

    Assessment of lumbar repositioning error

Eligibility Criteria

Criteria

Ages Eligible for Study:
35 Years to 45 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with CMLBP referred from orthopedic surgeon with no radicular pain

  • Their age is ranged between 35-55 years old (Martim etal.,2008)

  • BMI 24-28 kg/m2

Exclusion Criteria:
  • Patients who have a history of diabetic peripheral neuropathies

  • Patients who have a history of sciatica

  • Spinal or lower limb deformity or any pathology within the spine.

  • Patients who have neurological disorders

  • Patients who have a history of previous lumbar surgery

  • Patients who have visual problems

Contacts and Locations

Locations

Site City State Country Postal Code
1 October 6 university Giza Egypt 12511

Sponsors and Collaborators

  • October 6 University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Mai Hassan Ahmed Desouki, Assistant Lecturer, October 6 University
ClinicalTrials.gov Identifier:
NCT05047614
Other Study ID Numbers:
  • 153145
First Posted:
Sep 17, 2021
Last Update Posted:
Sep 17, 2021
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 17, 2021