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Video Movement Analysis Using Smartphones ViMAS: A Pilot Study
Published on: March 14, 2017
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Pilot Study of the EncephaLog Smartphone Application for Gait Analysis
Keren Tchelet1, Alit Stark-Inbar1, Ziv Yekutieli1
1Montfort Brain Monitor LTD, Ha-Nasi 14, Zichron Ya'acov 3090314, Israel.
Sensors (Basel, Switzerland)
|November 30, 2019
Summary
This study introduces EncephaLog, a smartphone app for detailed gait analysis, accurately measuring the Timed-Up-and-Go (TUG) test and 9 other biomarkers. It offers a simpler, more accessible instrumented TUG (iTUG) for clinical and home use.
Area of Science:
- Biomedical Engineering
- Gerontology
- Rehabilitation Technology
Background:
- Gait disorders and falls are prevalent in the elderly and various clinical conditions.
- Current evaluations of gait are often infrequent, subjective, and limited in scope.
- The Timed-Up-and-Go (TUG) test completion time is a key biomarker for mobility and fall risk prediction.
Purpose of the Study:
- To present EncephaLog, an extended smartphone application for detailed gait analysis.
- To assess the accuracy of EncephaLog in measuring TUG completion time and additional gait biomarkers.
- To evaluate EncephaLog as a simpler, more accessible alternative to traditional motion lab setups.
Main Methods:
- Development of the EncephaLog smartphone application utilizing accelerometers and gyroscopes.
- Conducting 32 TUG tests with four healthy adults.
- Simultaneous data collection using EncephaLog, motion capture cameras (MCC), pressure mats, and wearable sensors.
Main Results:
- EncephaLog accurately measured TUG completion time.
- High agreement was observed between EncephaLog-derived gait biomarkers and those from established motion lab equipment.
- The app provides 9 additional gait biomarkers beyond TUG completion time.
Conclusions:
- EncephaLog demonstrates potential as an accurate and simplified instrumented TUG (iTUG) platform.
- The app offers a cost-effective and space-efficient solution for clinical gait analysis and home monitoring.
- Further validation in larger, diverse patient populations is warranted.

