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Effects of Vertebral Axial Loading Walking Combined With Core Stabilization Exercises in Individuals With Chronic Low Back Pain

NCT07334782 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-01-19
Last updated
2026-02-02

Condition(s) studied

Chronic Low-back Pain (cLBP)

Investigational drug(s) / intervention(s)

Exercise - Core Stabilization Exercise ProgramCore Stabilization Exercises Plus Vertebral Axial Loading Walking Training

Exercise - Core Stabilization Exercise Program: Participants receive a physiotherapist-supervised core stabilization exercise program applied three sessions per week for six weeks. Before training, participants are educated about core muscle function and taught the abdominal bracing maneuver. Exercises are performed with neutral spinal alignment and controlled diaphragmatic breathing. Each session includes warm-up and cool-down exercises. The program consists of deep abdominal muscle activation, lower extremity movements with maintained trunk stability, bridging exercises, modified curl-up, and quadruped stabilization exercises. Exercises are demonstrated by the physiotherapist, performed with progressive repetitions, and corrected using verbal and manual feedback. The training is supervised by a physiotherapist and applied three sessions per week for six weeks.

Core Stabilization Exercises Plus Vertebral Axial Loading Walking Training: Participants receive the same core stabilization exercise program combined with vertebral axial loading proprioceptive walking training. Axial loading is applied through the vertex of the head using external weights ranging from 50 to 250 grams, adjusted according to individual tolerance. Walking is performed at a constant slow pace using a metronome set at 72 beats per minute. The initial walking distance is 40 meters and is progressively increased by 20 meters per week, reaching up to 140 meters. The intervention is supervised by a physiotherapist and applied three sessions per week for six weeks.

Study summary

Chronic low back pain is a common musculoskeletal condition persisting for more than three months and is associated with pain, functional limitations, impaired balance, altered proprioception, reduced trunk muscle performance, and decreased quality of life. Previous studies have demonstrated that individuals with chronic low back pain exhibit altered sensory input from spinal structures and impaired neuromuscular control, which may contribute to persistent pain and movement dysfunction. Although exercise-based physiotherapy approaches, particularly core stabilization exercises, are widely recommended and effective in the management of chronic low back pain, sensory deficits related to balance, proprioception, and body awareness are often insufficiently addressed in conventional rehabilitation programs.

Vertebral axial loading walking training is a functional rehabilitation approach involving slow, controlled walking under gentle vertical loading applied along the spinal axis. This intervention is thought to enhance afferent sensory input from spinal mechanoreceptors, potentially improving balance control, proprioception, and motor coordination. This randomized controlled study aims to investigate the effects of adding vertebral axial loading walking training to a standard core stabilization exercise program on pain intensity, balance, proprioception, trunk muscle strength and endurance, and body awareness in individuals with chronic low back pain.

Eligibility

Sex
ALL
Min age
30 Years
Max age
55 Years
Healthy volunteers
No
Inclusion Criteria: * Aged 30 to 55 years * Able to read and write * Not using regular medication during the study period * Voluntary participation and willingness to comply with study procedures Exclusion Criteria: * Presence of lumbar radiculopathy or neurological deficits * Presence of specific spinal pathologies, including scoliosis, kyphosis, malignancy, fracture, infection, or inflammatory joint or bone diseases * Presence of major or chronic systemic diseases, including diabetes mellitus, rheumatoid arthritis, or systemic lupus erythematosus * Presence of any neurological disease, such as stroke, Parkinson's disease, or multiple sclerosis * Presence of any condition affecting balance, including cerebellar ataxia, vertigo, Ménière's disease, inner ear labyrinthitis, or vestibular neuritis * History of spinal surgery * History of minimally invasive spinal procedures or injections, including platelet-rich plasma (PRP), growth factor-rich plasma (GFRP), corticosteroids, or other pharmacological injections * History of major lower extremity surgery, including knee arthroplasty, hip arthroplasty, high tibial osteotomy, or meniscal surgery * Presence of lower extremity musculoskeletal injuries, including meniscal or ligament injuries or chronic ankle instability * Presence of lower extremity deformities, including talipes equinovarus, genu varum, genu valgum, or coxa vara/valga * Presence of cognitive impairment or diagnosed psychiatric disorders * Pregnancy or being less than 6 months postpartum * History of cancer or ongoing cancer treatment * Illiteracy * Failure to attend three consecutive treatment sessions * Receipt of physical therapy or rehabilitation within the past 6 months

Primary outcome measure(s)

  • Change from Baseline in Lumbar Proprioception (Active Joint Position Sense) After 6 Weeks of Intervention — Baseline and 6 weeks
    Lumbar proprioception will be assessed by measuring active joint position sense during trunk flexion, lateral flexion, and extension using MATLAB-based angle analysis. The absolute angular error (in degrees) between the target position and the reproduced position will be calculated. Angular error is recorded in degrees, starting from 0° upward. Lower values indicate better proprioceptive accuracy. Higher values indicate impaired proprioception.
  • Change from Baseline in Pain Intensity at Rest and During Activity After 6 Weeks — Baseline and 6 weeks
    Pain intensity will be assessed using the Numeric Rating Scale (NRS). The scale ranges from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Lower scores indicate less pain.
  • Change from Baseline in Lumbar Pressure Pain Threshold After 6 Weeks — Baseline and 6 weeks
    Pressure pain threshold will be measured using a handheld algometer (Algometer commander, JTech Medical) and recorded in kg/cm². Higher values indicate greater pain tolerance, while lower values indicate increased pain sensitivity.
  • Change from Baseline in Trunk and Hip Muscle Strength After 6 Weeks — Baseline and 6 weeks
    Isometric muscle strength of trunk and hip muscles will be assessed using a digital hand-held dynamometer (Lafeyette Instrument®, Lafayette, IN) during maximal voluntary isometric contraction. Strength values are recorded in Newtons (N) or kilograms (kg). Higher values indicate greater muscle strength

Trial sites (1)

FacilityCityRegionStatus
Hacettepe University, Faculty of Physical Therapy and Rehabilitation Ankara Turkey (Türkiye)
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07334782 on ClinicalTrials.gov ↗ ← All trials in Turkey