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Clinical Trials in Turkey / NCT07119944
Active, not recruiting Observational

Pose Estimation and Inertial Measurement Unit Systems for Gait Analysis in Older Adults

NCT07119944 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2025-04-09
Last updated
2025-11-25

Condition(s) studied

Older Adults (65 Years and Older)

Investigational drug(s) / intervention(s)

Not Related

Not Related: This observational study does not involve any therapeutic intervention. Instead, all participants undergo gait analysis using two different measurement methods-2D pose estimation algorithms and an inertial measurement unit (G-Walk system)-to compare their outputs. Both assessments are performed on the same individuals under standardized conditions without altering their routine care.

Study summary

-This observational study aims to compare gait analysis performed using pose estimation algorithms with inertial measurement unit (IMU)-based gait analysis in older adults. Additionally, it aims to determine the reliability of gait analysis using pose estimation algorithms in this population.

The main questions it aims to answer are:

1. Are gait analyses using pose estimation algorithms consistent with those performed using an inertial measurement unit-based system in older adults?
2. Are gait analyses using pose estimation algorithms reliable in older adults?

Participants will take part in two measurement sessions. In the first session, they will be evaluated for inclusion criteria and general health status, and will complete gait analysis using both G-Walk (BTS Bioengineering) IMU sensors and a standard video camera simultaneously. In the second session, scheduled 1-3 days later, participants will perform only the 4-meter walking test, which will be recorded by video for pose estimation analysis.

Eligibility

Sex
ALL
Min age
60 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Ability to walk independently * Mini-Mental State Examination (MMSE) score ≤ 23/30 Exclusion Criteria: * Inability to walk independently for more than 20 meters without assistive devices * Inability to understand or comply with test instructions * Lack of consent to participate * Presence of severe neurological, musculoskeletal, cardiac, or psychological disorders

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Dokuz Eylul University, Faculty of Physical Therapy and Rehabilitation Izmir Balcova

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07119944 on ClinicalTrials.gov ↗ ← All trials in Turkey