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

Sponsor
Gaziler Physical Medicine and Rehabilitation Education and Research Hospital
Study ID
NCT07603609
Status
Recruiting
Apply to this trial

Conditions

  • Low Back Pain

Eligibility Criteria

Sex
ALL
Age
18 Years - 55 Years
Healthy Volunteers
Not accepted

Interventions

  • Huber 360 Sensorimotor Training — DEVICE
    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 — BEHAVIORAL
    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 Details

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.

Key Dates

First listed
May 22, 2026
Start date
May 4, 2026
Status verified
May 2026
Primary completion
Oct 30, 2026
Completion
Nov 30, 2026

Study Design

Enrollment
44 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Active Comparator: Home Exercise Program
    Participants in this group 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.
  • Experimental: Huber 360 Sensorimotor Training
    Participants in this group will receive a sensorimotor training protocol using the Huber 360 balance system. The intervention will include progressive rotational and oscillatory exercises aimed at improving proprioception, balance, neuromuscular control, and movement control. Sessions will be performed for 30 minutes, twice weekly for 5 weeks.

Primary Outcome Measure

Lumbar Proprioception Assessment [ Time Frame: Before treatment and immediately after completion of the 5-week intervention program ]

Central Contacts

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