GYKO-Based L-Test Reliability in Parkinson's Disease

NCT ID: NCT07327346

Last Updated: 2026-01-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Total Enrollment

25 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-12-01

Study Completion Date

2026-05-01

Brief Summary

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This study aims to investigate the interrater and test-retest reliability of GYKO-based postural sway measurements collected during the L-Test and Timed Up and Go (TUG) test in individuals with Parkinson's disease (Hoehn \& Yahr stages 1-3). Two independent raters will perform GYKO-based assessments of the L-Test and TUG with a 20-minute interval. Participants will return one week later to repeat the same procedures for test-retest reliability. Concurrent validity will be examined using the Berg Balance Scale.

Detailed Description

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This study aims to investigate the test-retest and interrater reliability, as well as the concurrent validity, of GYKO-based postural sway measurements obtained during the L-Test and the Timed Up and Go (TUG) test in individuals with Parkinson's disease. Participants diagnosed with idiopathic Parkinson's disease (Hoehn \& Yahr stages 1-3) will be evaluated using the GYKO inertial measurement unit, which provides quantitative postural sway parameters including ellipse area, mean length, mediolateral and anteroposterior mean length, mediolateral and anteroposterior mean distance, and velocity.

Two independent raters will perform GYKO-based assessments of the L-Test and TUG on the same day, with a 20-minute interval between raters, to determine interrater reliability. Participants will return one week later to repeat the same procedures, allowing assessment of test-retest reliability.

To examine concurrent validity, participants' functional balance will also be assessed using the Berg Balance Scale, and correlations between GYKO variables and clinical mobility tests (L-Test and TUG) will be analyzed.

Conditions

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Parkinson Disease

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Study Groups

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Parkinson's disease group

Parkinson's disease patients with stage 1-3 hoehn yahr

GYKO-Based Postural Sway Assessment

Intervention Type OTHER

This procedure involves obtaining postural sway parameters using the GYKO inertial measurement device during the Time Up and Go (TUG) test and L-Test. No therapeutic intervention is applied.

Time Up and Go Test: Timed Up and Go (TUG) is a standardized functional mobility test used to assess dynamic balance and gait performance. Participants are instructed to stand up from a standard-height chair, walk 3 meters, turn around, walk back to the chair, and sit down. The total time to complete the task (in seconds) is recorded. Higher times indicate reduced mobility.

L Test: Time (in seconds) to complete the L-Test of Functional Mobility. The test requires participants to stand up from a chair, walk 3 m, execute a 90° turn, walk another 7 m, perform a 180° turn, and return along the same path (total walking distance ≈ 20 m). The task ends when the participant sits back down. The total time to complete the task (in seconds) is recorded. Higher times indicate reduced mobility.

Interventions

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GYKO-Based Postural Sway Assessment

This procedure involves obtaining postural sway parameters using the GYKO inertial measurement device during the Time Up and Go (TUG) test and L-Test. No therapeutic intervention is applied.

Time Up and Go Test: Timed Up and Go (TUG) is a standardized functional mobility test used to assess dynamic balance and gait performance. Participants are instructed to stand up from a standard-height chair, walk 3 meters, turn around, walk back to the chair, and sit down. The total time to complete the task (in seconds) is recorded. Higher times indicate reduced mobility.

L Test: Time (in seconds) to complete the L-Test of Functional Mobility. The test requires participants to stand up from a chair, walk 3 m, execute a 90° turn, walk another 7 m, perform a 180° turn, and return along the same path (total walking distance ≈ 20 m). The task ends when the participant sits back down. The total time to complete the task (in seconds) is recorded. Higher times indicate reduced mobility.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Diagnosis of idiopathic Parkinson's disease
* Hoehn \& Yahr stage 1-3
* Ability to walk independently with or without an assistive device
* Ability to follow verbal instructions
* Age 50-85

Exclusion Criteria

* Other neurological, vestibular, or musculoskeletal disorders affecting balance
* Deep brain stimulation (DBS) implant
* Severe visual or auditory impairment
Minimum Eligible Age

50 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hasan Kalyoncu University

OTHER

Sponsor Role lead

Responsible Party

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Büşra Akıncı

MSc

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Büşra Akıncı, MSc

Role: STUDY_CHAIR

Hasan Kalyonuc University

Günseli Usgu, Assoc. Prof.

Role: STUDY_DIRECTOR

Hasan Kalyoncu University

Saadet Nur Çörekçioğlu, P.T.

Role: PRINCIPAL_INVESTIGATOR

Hasan Kalyoncu University

Locations

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Hasan Kalyoncu University

Gaziantep, Şahinbey, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

References

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Haas B, Clarke E, Elver L, Gowman E, Mortimer E, Byrd E. The reliability and validity of the L-test in people with Parkinson's disease. Physiotherapy. 2019 Mar;105(1):84-89. doi: 10.1016/j.physio.2017.11.218. Epub 2017 Dec 5.

Reference Type BACKGROUND
PMID: 29395266 (View on PubMed)

Zampieri C, Salarian A, Carlson-Kuhta P, Aminian K, Nutt JG, Horak FB. The instrumented timed up and go test: potential outcome measure for disease modifying therapies in Parkinson's disease. J Neurol Neurosurg Psychiatry. 2010 Feb;81(2):171-6. doi: 10.1136/jnnp.2009.173740. Epub 2009 Sep 2.

Reference Type BACKGROUND
PMID: 19726406 (View on PubMed)

Other Identifiers

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HKU/PH/2

Identifier Type: -

Identifier Source: org_study_id

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