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Usefulness of static posturography with reference to established subjective clinical examination

Postural stability in patients with osteoarthritis of the lumbosacral spine using posturography

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12619001416189
Enrollment
49
Registered
2019-10-15
Start date
2019-10-28
Completion date
2020-01-28
Last updated
2019-10-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Background. Spinal pain syndrome, commonly referred to as low back pain, is a scourge of our times. Objective. The aim of the study will be evaluate the usefulness of static posturography in monitoring the progress of rehabilitation in a group of patients with lumbosacral pain syndrome.

Interventions

The study group will be consisted of randomly selected patients of both sexes, undergoing treatment for lumbosacral discogenic pain syndrome due to degenerative spondyloarthropathy, with no history of hip or knee osteoarthritis, as the latter could manifest with pain radiating to the lumbosacral segment of the spine. The diagnosis will be established based on medical history, physical examination, and radiographic assessments (anteroposterior and lateral X-ray films, magnetic resonance imaging,

The study group will be consisted of randomly selected patients of both sexes, undergoing treatment for lumbosacral discogenic pain syndrome due to degenerative spondyloarthropathy, with no history of hip or knee osteoarthritis, as the latter could manifest with pain radiating to the lumbosacral segment of the spine. The diagnosis will be established based on medical history, physical examination, and radiographic assessments (anteroposterior and lateral X-ray films, magnetic resonance imaging, or computed tomography). All study subjects will be underwent static posturography, rated their pain severity based on a visual analog scale (VAS), and had their physical functioning will be evaluated with a modified WOMAC questionnaire. These assessments will be conducted in the morning on the first and final days of the rehabilitation course, before the rehabilitation treatments scheduled for those days, and after approximately three months (± 2 weeks) after rehabilitation course completion. The study group will be underwent a 15-day course of physiotherapy, including: relaxation-promoting positioning- reducing load on the lumbosacral spine by a system of slings with knees and hips bending to angle of 90 degrees (about 30 min. once daily,the duration of administration, 3 weeks) , magnetotherapy (frequency with f=2-50Hz, field intensity of 2.5-5 mT and duration of 15 minutes, once daily,the duration of administration, 3 weeks), hydrocortisone iontophoresis at the trigger point in the lumbosacral region(2% hydrocortisonum, once daily,the duration of administration, 3 weeks) , interferential current (f=1–100 Hz) , special exercises for strengthening core and lower extremity muscles, intended for patients with spondyloarthropathies, isometric exercises, general fitness exercises, proprioception exercises for the lower extremities and spine, water exercises-about 30 min. once daily,the duration of administration, 3 weeks and patient education on preventing low back overload - guidance on prevention of low back pain for example in work, sitting position, activities of daily living etc. Education will be provided in whole 15-day course of physiotherapy on each session. It will be provided by certificated physiotherapist with PhD or MSc degree. Participants with osteoarthritis of the lumbosacral spine will be patients of the Department of Rehabilitation of the Independent Public Central Clinical Hospital in Warsaw. Pedobarographic measurements will be collected using a WIN-POD Pel 38 electronic podometer and WIN-POD 3.81 software at a frequency (f) of 100 Hz per 30 seconds. To ensure uniform data collection and reliable results, examiners will be asked to adhere to a strict study protocol that included asking participants a series of questions prior to the test about conditions that could adversely affect postural stability. The questions will be designed to assess overall well-being, medication intake, number of hours of sleep, alcohol consumption, history of excessive physical exercise, and current pain or discomfort. The examination will be consisted of four, 30-second tests with 60-second intermissions in the sitting position. The first two pedobarographic tests will be performed with eyes open (EO) in freestanding posture, whereas the third and fourth tests will be performed with eyes closed (EC). The participants will be asked to remove their shoes and stand upright on the forceplate with the head erect and their arms hanging loosely by their sides. Also they will be asked to stand (barefoot) on a floor-based foot pressure measurement device as pedobarographic balance measurements of deviation length, area and velocity from center of gravity will be recorded. All tests will be conducted in a quiet room with normal temperature and the same illumination. WIN-POD electronic podometer will be calibrated prior to the recordings and further underwent an automatic calibration check before each trial.

Sponsors

Bartosz Slomka
Lead SponsorIndividual

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Treatment
Masking
Blinded (masking used) (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
30 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

diagnosed lumbosacral discogenic pain syndrome due to degenerative spondyloarthropathy confirmed consent agree to participate in study pain severity based on a visual analog scale (VAS) >4 a positive lasegue's test (also called straight leg raise, SLR test) not consumption of analgesic, psychotropic or other medicines that could affect equilibrium responses

Exclusion criteria

musculoskeletal pain, advanced foot deformities, intake of analgesic drugs, functional shortening of more than 15 mm of a lower limb,balance disorder,overall poor well-being, pregmancy, declared consumption of alcohol within 24 hours of the test and less than 6 hours of sleep, single/total hip or knee arthroplasty.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026