CClinicalTrials.gg
Status unknownNCT05047614Updated Sep 17, 2021

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

An interventional study of including sham in Orthopedic Disorder, sponsored by October 6 University. Status unknown at 1 site in Egypt. Open to female participants aged 35 Years to 45 Years. Per ClinicalTrials.gov, last updated 2021-09-17.

Sponsored by October 6 University · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Sep 2021), so the status shown — last known as Recruiting — may be out of date.

From the registry’s dates

  • Registered 3 months after the study started (first participant enrolled Apr 2020, registered Jul 2020).
Phase
Not applicable
Study type
Interventional
Enrollment
48
Allocation
Randomized
Ages
35 Years to 45 Years
Sex
Female
01

Study 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?

Read the 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

02

Conditions studied

03

In context

Musculoskeletal Diseases

657 studies on the registry are indexed under Musculoskeletal Diseases; 159 are open to participants now.

This study's planned enrollment of 48 is below the median of 73 across 438 interventional studies indexed under Musculoskeletal Diseases.

Browse Musculoskeletal Diseases studies →

Lead sponsor

October 6 University is the lead sponsor of 135 studies on the registry; 27 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
35 Years to 45 Years
Sexes eligible
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

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
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Factorial assignment
Masking
Single (Participant)
Enrollment
48 participants (estimated)

Study arms

  • Experimental
    Study 1

    Twelve patients in study group 1 receiving lumbar repositioning feedback training

    Device: including sham

  • Experimental
    Study 2

    Twelve patients in study group 2 receiving transverses abdominis training

    Device: including sham

  • Experimental
    Study 3

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

    Device: including sham

  • Experimental
    Control

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

    Device: including sham

Interventions

  • Deviceincluding sham

    Repositiong feedback training and biofeedback pressure training unit

06

What researchers measure

Primary outcomes

  1. Pressure biofeedback unit

    Assessment of transversus abdominis activation

    Time frame: up to 45 days

  2. feedback laser tracker

    Assessment of lumbar repositioning error

    Time frame: up to 45 days

07

Study locations

1 of 1 sites recruiting
  • October 6 university
    Giza, 12511, Egypt
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 17, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05047614
Lead sponsor
October 6 University
Responsible party
Mai Hassan Ahmed Desouki (Assistant Lecturer, October 6 University) — Principal investigator
First posted
Sep 17, 2021
Start date
Apr 19, 2020
Primary completion
May 2, 2022 (estimated)
Completion
Aug 15, 2022 (estimated)
Last update
Sep 17, 2021

Study contacts

MAI HASSAN, Doctoral
Contact
Mai.Hassan.ph@o6u.edu.eg
01019461836
Hossam Magdy, Doctoral
Contact
Hosam.Magdy.PT@o6u.edu.eg
01112730605

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Sep 2021. You cannot join it, but the record below documents what was studied.

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