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Evaluation of Stabilization Training With Biofeedback in Lumbosacral Spine Pain Syndrome

RecruitingNAAges 30 Years - 65 YearsAllUniversity of Rzeszow
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In plain words

What the trial is, and whether it could suit you

The aim of the study is to evaluate the effects of biofeedback-assisted stabilization training and conventional therapy on pain perception, balance, spinal mobility, functional performance, physical activity, stress level, and quality of life in patients with lumbosacral spine pain syndrome treated conservatively. The main research questions the study seeks to answer are as follows: Whether and to what extent the implemented therapeutic program improves balance, spinal mobility, functional performance, physical activity, quality of life, and reduces pain perception and stress levels in patients with lumbosacral spine pain syndrome? Are there differences in therapeutic outcomes depending on the treatment method applied? Are the therapeutic effects maintained three months after completion of the intervention? Researchers will compare two groups: a control group and an experimental group. I

Sign in to get the eligibility rules as simple questions to take to your doctor.

📋 Eligibility rules (as published)
Inclusion Criteria: * Diagnosed chronic lumbosacral spine pain syndrome (score \>4 on the Keele STarT Back Screening Tool) * Lumbosacral pain intensity \>3 on the Visual Analog Scale (VAS) persisting for at least the past 3 months * Age between 30 and 65 years * No concurrent participation in another rehabilitation program * Provision of written informed consent to participate in the study Exclusion Criteria: * Acute phase of lumbosacral spine pain syndrome * Presence of neurological symptoms such as paresthesia, dysesthesia, impaired superficial sensation, impaired pain sensation, muscle strength below grade 3 on the Lovett scale in the lower limbs, sphincter dysfunction, or cauda equina syndrome * Recent fractures of the spine or pelvis (less than 6 months since injury) * Segmental instability confirmed by functional X-ray or magnetic resonance imaging (MRI) * Spondylolisthesis greater than Grade I according to the Meyerding classification * Coexisting neurological (e.g., Parkinson's disease, neuropathies), autoimmune (e.g., ankylosing spondylitis), orthopedic (lower limb disorders), or oncological diseases * Pregnancy * Active use of analgesic or anti-inflammatory pharmacotherapy (e.g., steroids, NSAIDs) * Concurrent participation in other rehabilitation programs or failure to complete the 8-week therapy program * Completion of any structured rehabilitation program within the past 3 months * Lack of informed consent to participate in the study
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What it tests

  • Standard Rehabilitation
  • Biofeedback Ultrasonography
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Where

1 site
Medical and Rehabilitation Center in Tarnów Reha Medica
Tarnów, Poland
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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