- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06108466
RELIABILITY AND VALIDITY OF THE DT BALANCE TEST IN PATIENTS WITH TKA (DT TKA)
October 25, 2023 updated by: Damla Ozcan, Dokuz Eylul University
RELIABILITY AND VALIDITY OF THE DUAL TASK BALANCE TEST IN PATIENTS WITH TOTAL KNEE ARTHROPLASTY
The ability to perform a cognitive task while walking simultaneously is essential in real daily life.
However, the psychometric properties of dual-task walking tests have not been well established in patients undergoing total knee arthroplasty (TKA).
The aim of study assess the test-retest reliability and validity of dual conditions TUG, 3MBWT, 8FWT nad 4SST in patients with TKA.
Study Overview
Status
Active, not recruiting
Conditions
Study Type
Observational
Enrollment (Actual)
31
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
İzmir, Turkey
- Dokuz Eylul University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Probability Sample
Study Population
Total Knee arthroplasty
Description
Inclusion Criteria: TKA -
Exclusion Criteria: revision knee arthroplasty
-
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Performance test
Time Frame: 1 Hour
|
Timed Up and Go Test
|
1 Hour
|
|
Performance Test
Time Frame: 1 hour
|
3MWT
|
1 hour
|
|
Perfromance Test
Time Frame: 1 hour
|
8 FWT
|
1 hour
|
|
Performance Test
Time Frame: 1 hour
|
4SST
|
1 hour
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Patient Reported
Time Frame: 1 hour
|
HSS Knee Score
|
1 hour
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 14, 2022
Primary Completion (Estimated)
November 12, 2023
Study Completion (Estimated)
November 25, 2023
Study Registration Dates
First Submitted
October 23, 2023
First Submitted That Met QC Criteria
October 25, 2023
First Posted (Actual)
October 31, 2023
Study Record Updates
Last Update Posted (Actual)
October 31, 2023
Last Update Submitted That Met QC Criteria
October 25, 2023
Last Verified
October 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 6749-GOA
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.