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Evaluation of Proprioception

Evaluate the Proprioception in Patients with Total Knee Arthroplasty

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03837041
Acronym
PROPRIO_TPG
Enrollment
71
Registered
2019-02-11
Start date
2017-03-01
Completion date
2021-12-31
Last updated
2024-09-19

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

Conditions

Proprioceptive Disorders

Keywords

total knee arthroplasty, Proprioception, osteoarthritis

Brief summary

The osteoarthritis (OA) is a chronic and degenerative disease which brings articular cartilage degeneration. As a consequence, balance and proprioception could be dangerously reduced after total knee arthroplasty. Several studies demonstrated the correlation between OA, proprioception reduction and increased risk of falling. The aim of this study is to evaluate the proprioception improvement in patients with total knee arthroplasty.

Interventions

OTHERReconditioning Proprioception

Proprioceptive training using Delos Postural Proprioceptive System

Sponsors

University of Bologna
CollaboratorOTHER
Istituto Ortopedico Rizzoli
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
45 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

are patients with ASA: 1, 2 or 3; patients who have given their informed written consent to participate in the study; patients live in Bologna and neighboring areas.

Exclusion criteria

are patients with previous osteotomy of the lower limbs; patients with post-traumatic arthrosis; patients with severe preoperative valgus deformity (Hip Knee Ankle angle\> 10 °); patients with BMI\> 40 kg / m2; patients with rheumatoid arthritis; patients with chronic inflammatory joint diseases; patients with walking diseases (amputations, neuro-muscular diseases, polio, hip dysplasias); patients with Severe arthrosis of the ankle (Kellgren-Lawrence\> 3); patients with Severe coxarthrosis (Kellgren-Lawrence\> 3); patients with severe postural instability; patients with cognitive impairments, patients with concomitant neurological diseases

Design outcomes

Primary

MeasureTime frameDescription
Improvement of a proprioception24 monthsStability Index (SI) in percentage the maximum is 100%

Secondary

MeasureTime frameDescription
Evaluation of performance in lower limb questionnaire24 monthsShort Physical Performance Battery - SPPB The score range from 0 (wost performance) to 12 (best performance)
KSS Score24 monthsThe score range from 0 to 100 with lower scores being indicative of worse knee conditions and higher scores being indicative of better knee conditions
Clinical score24 monthsWestern Ontario and McMaster Universities Osteoarthritis Index the WOMAC evaluates 3 dimensions: pain, stiffness, and physical function with 5, 2, and 17 questions, respectively. The Likert version of the WOMAC is rated on an ordinal scale of 0 to 4, with lower scores indicating lower levels of symptoms or physical disability.

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026