- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05054192
Reliability and Validity of Modified Four Square Step Test
Evaluation of Test-retest Reliability, Concurrent Validity and Minimal Detectable Change of the Modified Four Square Step Test in Individuals With Primary Total Hip Arthroplasty.
Study Overview
Status
Conditions
Detailed Description
Roos et al. improved the Modified Four-Square Step Test to complete the test by stroke patients and not to fall due to practices of the test while performing the test. The Modified Four Square Step Test variates from the The Four Square Step Test is that the person is not asked to look ahead during the test, and instead of using a cane, tapes are used to prevent people from losing their balance by tripping over the obstacle. Thus, although the height of the obstacle is reduced, the boundaries of the obstacle are preserved.
Functional improvements are reached in patients with primary total hip arthroplasty compared to the pre-operative term however some problems as continued range of motion limitations, loss of joint proprioception sensation, and resulting balance and gait disorders may result in failure of the Four Square Step Test. Therefore, the need for the apply of the Modified Four Square Step Test in individuals with primary THA is necessary. The aim of this study is to evaluate the test-retest reliability, concurrent validity and minimal detectable change of the Modified Four Square Step Test in individuals with primary total hip arthroplasty.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: EMEL TAŞVURAN HORATA, PhD
- Phone Number: +905547759663
- Email: ethorata@gmail.com
Study Locations
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-
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Afyonkarahisar, Turkey, 03030
- Recruiting
- Afyonkarahisar Health Science University
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Contact:
- EMEL TAŞVURAN HORATA, PhD
- Phone Number: +905547759663
- Email: ethorata@gmail.com
-
Principal Investigator:
- EMEL TAŞVURAN HORATA, PhD
-
Sub-Investigator:
- Fatma EKEN
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Sub-Investigator:
- MURAT YEŞİL, MD
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Sub-Investigator:
- ÖZAL ÖZCAN, Prof
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Being between the ages of 18-85.
- Having undergone primary total hip arthroplasty at least ≥6 months ago.
Exclusion Criteria:
- Having severe cardiovascular or lung disease
- Having severe dementia or communication difficulties
- Having a musculoskeletal or neurological problem that may affect participation in balance tests
- Having an uncorrectable visual impairment
- Having a body mass index of more than 40 kg/m2
Study Plan
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Dynamic Balance
Time Frame: 6 minutes
|
Dynamic balance is the ability of an object to balance while in motion or switching between positions.
Dynamic balance will be evaluated with the modified four square step test.
The duration as second will be recorded.
|
6 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Dynamic Balance
Time Frame: 4 minutes
|
Dynamic balance will be evaluated with the timed and go test and the test completion time will be recorded in seconds.
|
4 minutes
|
Dynamic Balance
Time Frame: 25 minutes
|
Dynamic balance will be evaluated with the Berg Balance Test.
The scores from the test will be recorded.
|
25 minutes
|
Collaborators and Investigators
Investigators
- Principal Investigator: Emel TAŞVURAN HORATA, PhD, Afyonkarahisar Health Science University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2021/414
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
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