Assessing gait using a smartphone application

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the effectiveness of the Gait-Analyzer smartphone application compared to traditional 3D computerized gait analysis. Healthy participants aged 18 to 26 will be recruited and divided into two groups to undergo both types of gait analysis. The aim is to determine the validity and reliability of the smartphone application in assessing human gait, which is crucial for clinical decision-making. By leveraging the accessibility of smartphone technology, the study seeks to address the limitations of conventional gait analysis methods.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Age between 18 and 26 years.
* Body Mass Index (BMI) within normal limits (18.5-24.9 kg/m2)

Exclusion Criteria:

* Presence of lower extremity rotational problems (such as high femoral anteversion, internal tibial torsion, 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

Where it's running

• Acibadem Mehmet Ali Aydinlar University
  Istanbul, Turkey (Türkiye) Recruiting

Study contacts

• Principal investigator: Ayşenur Erekdağ, MSc — Bezmialem Vakif University
• Study coordinator: Ayşenur Erekdağ, MSc
• Email: aysenurerekdag@gmail.com
• Phone: 05548959013

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.