Validity And Reliability Of The Short Physical Performance Battery In Patients Undergoing Total Knee Arthroplasty
Investigation Of The Validity And Reliability Of The Short Physical Performance Battery In Patients Undergoing Total Knee Arthroplasty
1 other identifier
interventional
45
1 country
1
Brief Summary
Objectives: Practical, applicable, valid, and reliable tools are needed to assess physical performance in patients with Total Knee Arthroplasty(TKA) in a variety of settings, including routine clinical assessment, research studies, and community-based programs. Therefore, the aim of this study is to evaluate the validity and reliability of the Short Physical Performance Battery (SPPB) among patients with TKA. Methods: We included patients who underwent TKA surgery. The SPPB, Timed up and go(TUG) test and, Hospital for Special Surgery (HSS) Knee Score were administered to the patients. SPPB was performed twice on the same day with 1 h rest.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable knee-osteoarthritis
Started Jan 2022
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 2, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 12, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
February 12, 2023
CompletedFirst Submitted
Initial submission to the registry
January 2, 2024
CompletedFirst Posted
Study publicly available on registry
January 11, 2024
CompletedJanuary 11, 2024
January 1, 2024
1.1 years
January 2, 2024
January 2, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Short Physical Performance Battery
1 Hour
Secondary Outcomes (1)
TUG
15 minutes
Interventions
Performance Test
Eligibility Criteria
You may qualify if:
- patients who had primary TKA surgery at six months ago, were diagnosed with preoperative knee OA, and were willing to participate in the research
You may not qualify if:
- a previous orthopedic, neurological, or systemic disease that effected walking or standing, body mass index of 40 kg / m2 and over and having any other surgery on the same limb that effected walking.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Dokuz Eylul University
Izmir, Turkey (Türkiye)
Related Publications (1)
Ozcan D, Unver B, Karatosun V. Investigation of the validity and reliability of the short physical performance battery in patients undergoing total knee arthroplasty. Physiother Theory Pract. 2025 Feb;41(2):370-376. doi: 10.1080/09593985.2024.2337784. Epub 2024 Apr 1.
PMID: 38557264DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Msc. Pt
Study Record Dates
First Submitted
January 2, 2024
First Posted
January 11, 2024
Study Start
January 2, 2022
Primary Completion
February 12, 2023
Study Completion
February 12, 2023
Last Updated
January 11, 2024
Record last verified: 2024-01
Data Sharing
- IPD Sharing
- Will not share