🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Turkey / NCT07603609
Recruiting Not applicable

Sensorimotor Training With a Mobilized Balance Platform in Patients With Chronic Low Back Pain

NCT07603609 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-05-04
Last updated
2026-05-22

Condition(s) studied

Low Back Pain

Investigational drug(s) / intervention(s)

Huber 360 Sensorimotor TrainingHome Exercise Program

Huber 360 Sensorimotor Training: Participants will receive sensorimotor training using the Huber 360 balance system. The protocol will include progressive rotational and oscillatory exercises designed to improve proprioception, balance, neuromuscular control, and movement control in patients with chronic low back pain. Sessions will be performed for 30 minutes, twice weekly for 5 weeks.

Home Exercise Program: Participants will perform a home exercise program including warm-up and stretching exercises, spinal mobility exercises, lumbopelvic control exercises, and balance exercises. The program will be performed for 30 minutes per session, twice weekly for 5 weeks.

Study summary

This randomized controlled study aims to investigate the effects of a sensorimotor training protocol using a mobilized balance platform device on proprioceptive system function, movement control, balance, physical performance, pain severity, and quality of life in patients with chronic low back pain. A total of 44 patients with chronic low back pain will be recruited from the outpatient clinic of Gaziler Physical Medicine and Rehabilitation Training and Research Hospital.

Participants will be randomly assigned to either a sensorimotor training group or a control group. The intervention group will receive sensorimotor training using the Huber 360 balance system, while the control group will perform a home exercise program including stretching, spinal mobility, lumbopelvic control, and balance exercises.

Pain severity, proprioception, functional status, balance, physical performance, and quality of life will be assessed before and after treatment by an assessor blinded to group allocation.

Eligibility

Sex
ALL
Min age
18 Years
Max age
55 Years
Healthy volunteers
No
Inclusion Criteria: * Individuals aged between 18 and 55 years * Presence of chronic low back pain lasting at least 3 months * Pain intensity score of 3 or higher on the Visual Analog Scale (VAS) * Individuals with sufficient cognitive ability to understand and follow study procedures * Willingness to participate voluntarily in the study Exclusion Criteria: * Participation in a similar training program within the last 12 months * History of lower extremity or spinal surgery * Presence of non-mechanical low back pain, inflammatory disease, or tumor * Uncontrolled hypertension or cardiac disease * History of malignancy * Presence of radicular symptoms associated with low back pain * Progressive neurological deficits * Neurogenic claudication

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Ankara Gaziler physical therapy and rehabilitation hospital Ankara Turkey (Türkiye) Recruiting

More Gaziler Physical Medicine and Rehabilitation Education and Research Hospital trials in Turkey

Other trials for the same condition

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 NCT07603609 on ClinicalTrials.gov ↗ ← All trials in Turkey