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Clinical Trials/NCT06150170
NCT06150170CompletedNot Applicable

Evaluation of the Efficiency of Propioceptive Study According to Radiological Stages in Patients With Knee Osteoarthritis

Istanbul University1 site in 1 country34 target enrollmentStarted: November 21, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
34
Locations
1
Primary Endpoint
The Western Ontario and McMaster Universities Arthritis Index (WOMAC)

Study Overview

Brief Summary

Evaluation of the Efficiency of Propioceptive Study According to Radiological Stages in Patients with Knee Osteoarthritis

Detailed Description

Investigators divided patients with knee osteoarthritis into two groups. Group 1 consisted of stage 1 and stage 2 patients. Group 2 consisted of stage 3 and stage 4 patients. Proprioceptive training was applied in both groups. Investigators aim is to evaluate the effect of proprioceptive exercises on knee osteoarthritis according to the radiological level.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Eligibility Criteria

Ages
35 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Diagnosed with knee osteoarthritis by a specialist physician using MRI, US or radiography and physical examination.
  • •Being between the ages of 35-70
  • •Stage 1-2-3-4 according to Kellegran Lawrence (K-L) in radiological examination

Exclusion Criteria

  • •Having active synovitis
  • •Having received physical therapy in the last 6 months
  • •Those with neurological problems that affect walking
  • •Those with serious respiratory, central, peripheral, vascular and uncontrolled metabolic problems that will prevent exercise
  • •Has had lower extremity surgery in the past
  • •Intra-articular steroid injections within the last 6 months
  • •Using psychoactive drugs
  • •Those with serious vision, hearing and speech disorders
  • •Patients with vestibular dysfunction will not be included in the study

Arms & Interventions

Group 1

Experimental

This group includes patients with grade 1 and grade 2 knee osteoarthritis.

Intervention: Proprioceptive training (Other)

Group 2

Experimental

This group includes patients with grade 3 and grade 4 osteoarthritis.

Intervention: Proprioceptive training (Other)

Outcomes

Primary Outcomes

The Western Ontario and McMaster Universities Arthritis Index (WOMAC)

Time Frame: Evaluation will be performed before treatment and after 4 weeks rehabilitation program.

The scale consists of 3 main headings and 24 questions. It is scored between 0 and 100. There is a negative correlation between scoring and functionality.

Secondary Outcomes

  • Visual Analogue Scale (VAS)(Evaluation will be performed at Baseline (before treatment) and 4 weeks)
  • Pressure Pain Threshold Measurement(Evaluation will be performed at Baseline (before treatment) and 4 weeks)
  • Manual Muscle Test(Evaluation will be performed at Baseline (before treatment) and 4 weeks)
  • Proprioception Sense(Evaluation will be performed at Baseline (before treatment) and 4 weeks)
  • Timed Up and Go Test (TUG)(Evaluation will be performed at Baseline (before treatment) and 4 weeks)
  • Short Form 36 (SF-36)(Evaluation will be performed at Baseline (before treatment) and 4 weeks)
  • Range of Motion (ROM)(Evaluation will be performed at Baseline (before treatment) and 4 weeks)
  • Global Rating of Change (GRC) Scale(4 weeks)
  • International Physical Activity Scale (IPAQ)(Evaluation will be performed at Baseline (before treatment) and 4 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Sibel Gayretli Atan

Physiotherapist

Istanbul University

Study Sites (1)

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