Actively Recruiting

Age: 18Years - 26Years
All Genders
NCT06157749

Gait Assessment Via Telephone Application

Led by Istanbul University - Cerrahpasa · Updated on 2025-03-24

34

Participants Needed

1

Research Sites

56 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The evaluation of human gait is a crucial component of the clinical assessment and decision-making process. The gold standard in gait analysis is computerized gait analysis, which allows for three-dimensional digital data acquisition through computers (3D Computerized Gait Analysis). However, this technology is not readily accessible in routine analyses, as it proves to be a time-consuming and expensive endeavor in terms of infrastructure and human resources. The utilization of smartphones in clinical applications is on the rise, facilitated by the increasing accessibility of low-cost or free "applications," thereby addressing the limitations associated with traditional gait analysis methods. The Gait-Analyzer application is among the mentioned applications. However, in the literature, no evidence has been found regarding the validity and reliability of Gait-Analyzer application compared to the gold standard 3D computerized gait analysis systems within the context of gait analyses. The aim of this study is to comparatively examine the effectiveness of the Gait-Analyzer smartphone application with established 3D Computerized Gait Analysis systems, which have proven validity and reliability in gait analyses. Through this research, the study intends to elucidate the validity and reliability of spatiotemporal parameters of walking within the Gait-Analyzer smartphone application.

CONDITIONS

Official Title

Gait Assessment Via Telephone Application

Who Can Participate

Age: 18Years - 26Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 26 years
  • Body Mass Index (BMI) within normal limits (18.5-24.9 kg/m2)
Not Eligible

You will not qualify if you...

  • Presence of lower extremity rotational problems such as high femoral anteversion, internal tibial torsion, or metatarsus adductus
  • History of Botulinum Toxin Type A (BoNT-A) application or surgery within the last 6 months
  • History of lower extremity injury within the last 6 months
  • Leg length discrepancy
  • Presence of third-degree pes planus
  • Any neurological, rheumatic, musculoskeletal, metabolic, or connective tissue diseases
  • History of pain, deformity, or surgery related to the vertebral column and upper extremities
  • Presence of cognitive, mental, and/or severe psychiatric disorders

AI-Screening

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Trial Site Locations

Total: 1 location

1

Acibadem Mehmet Ali Aydinlar University

Istanbul, Turkey (Türkiye), 34752

Actively Recruiting

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Research Team

A

Ayşenur Erekdağ, MSc

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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