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Effects of Mobilized Balance Platform Exercises on Balance Parameters in Patients With Knee Osteoarthritis

Effects of Mobilized Balance Platform Exercises on Balance Parameters, Functional Status, and Pain in Patients With Knee Osteoarthritis: A Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07575425
Enrollment
36
Registered
2026-05-08
Start date
2026-05-04
Completion date
2026-10-30
Last updated
2026-05-08

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

Conditions

Knee Arthritis, Osteoarthritis, Osteearthritis

Brief summary

This prospective single-blind randomized controlled study aims to investigate the effects of mobilized balance platform exercises on balance parameters, pain, functional status, fear of falling, and kinesiophobia in patients with knee osteoarthritis. A total of 36 patients diagnosed with knee osteoarthritis will be recruited from the outpatient clinic of Gaziler Physical Medicine and Rehabilitation Training and Research Hospital. Participants will be randomly assigned to one of two groups. The control group will receive conventional physical therapy including transcutaneous electrical nerve stimulation (TENS) and a home exercise program consisting of knee strengthening, balance, range of motion, proprioceptive, and stretching exercises. The intervention group will receive the same conventional treatment in addition to mobilized balance platform exercises using the Huber 360 system. Pain severity, functional status, balance parameters, fear of falling, and kinesiophobia will be evaluated before and after treatment by an assessor blinded to treatment allocation.

Interventions

DEVICEHuber 360 Balance Training

Participants will perform mobilized balance platform exercises using the Huber 360 system. The exercise protocol will include quadriceps and core strengthening, proprioceptive training, balance exercises, and neuromuscular exercises specifically designed for patients with knee osteoarthritis. Sessions will be performed 3 times per week for 20 minutes.

OTHERConventional Physical Therapy

Participants will receive conventional physical therapy including transcutaneous electrical nerve stimulation (TENS) and a home exercise program consisting of knee strengthening, balance, range of motion, proprioceptive, and stretching exercises performed 3 times per week for 20 minutes.

Sponsors

Gaziler Physical Medicine and Rehabilitation Education and Research Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
45 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Patients aged between 45 and 65 years * Diagnosis of knee osteoarthritis classified as Kellgren-Lawrence grade 2 or 3 * Willingness to participate voluntarily in the study

Exclusion criteria

* Presence of orthopedic knee implants * Kellgren-Lawrence grade 1 or grade 4 knee osteoarthritis * Sensory impairment * Diagnosis of malignancy * Unhealed fractures * Circulatory disorders * Infection around the knee joint * Severe hearing loss or visual impairment * Cognitive impairment * Uncontrolled hypertension or diabetes mellitus * Vestibular disorders causing balance problems, such as vertigo * Use of walking assistive devices such as canes or walkers

Design outcomes

Primary

MeasureTime frameDescription
Static and Dynamic Balance ParametersBefore treatment and immediately after completion of the 8-week treatment programBalance performance will be assessed using the Huber 360 balance assessment system. Measurements will include static balance with eyes open and eyes closed, single-leg balance performance, and limits of stability.

Secondary

MeasureTime frameDescription
Pain Severity Assessed by Visual Analog Scale (VAS)Before treatment and immediately after completion of the 8-week treatment programPain intensity will be assessed using a 10-cm Visual Analog Scale (VAS) for night pain, resting pain, and pain during movement. Higher scores indicate greater pain severity.
Functional Status Assessed by WOMACBefore treatment and immediately after completion of the 8-week treatment programFunctional status will be evaluated using the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). Higher scores indicate worse pain, stiffness, and functional limitation.
Functional Mobility Assessed by Timed Up and Go TestBefore treatment and immediately after completion of the 8-week treatment programFunctional mobility and dynamic balance will be assessed using the Timed Up and Go Test. Shorter completion times indicate better functional mobility.
Fear of Falling Assessed by the International Falls Efficacy ScaleBefore treatment and immediately after completion of the 8-week treatment programFear of falling during activities of daily living will be evaluated using the International Falls Efficacy Scale. Higher scores indicate greater concern about falling.
Kinesiophobia Assessed by Tampa Scale for KinesiophobiaBefore treatment and immediately after completion of the 8-week treatment programFear of movement and reinjury will be evaluated using the Tampa Scale for Kinesiophobia. Higher scores indicate greater fear of movement.

Countries

Turkey (Türkiye)

Contacts

CONTACTSEFA GÜMRÜK ASLAN
sefagumrukk@gmail.com+903122911503
PRINCIPAL_INVESTIGATORSefa Gümrük Aslan

gaziler physcial therapy and rehabilitation hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 9, 2026