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NCT Number: NCT07499063

Effect of Exoskeleton-Assisted Walking on Gait Parameters in Healthy Adults

This study aims to evaluate the immediate effects of a single session of exoskeleton-assisted walking on gait parameters and plantar pressure distribution in healthy young adults. Participants will undergo baseline gait assessment using a baropodometric platform, followed by a 30-minute walking session using the Ekso NR exoskeleton. Immediately after the intervention, gait assessment will be repeated. The study is designed as a single-group, pre-post experimental evaluation of biomechanical changes associated with exoskeleton use.

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Key information

Age range

19 year–25 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

The purpose of this study is to investigate the immediate biomechanical effects of exoskeleton-assisted walking in healthy individuals. A total of 25 healthy adult participants will be recruited. After screening for eligibility, participants will complete a questionnaire and undergo baseline gait analysis using a baropodometric platform (FreeStep).

Following the baseline assessment, participants will perform a 30-minute walking session using the Ekso NR wearable exoskeleton under supervision. Immediately after completing the session, gait analysis will be repeated using the same baropodometric platform.

Primary outcomes will include changes in plantar pressure distribution parameters, while secondary outcomes will include changes in spatiotemporal gait parameters such as step length, cadence, and symmetry.

The study is designed as a single-arm, pre-post interventional study focusing on biomechanical assessment rather than therapeutic intervention. The results will contribute to understanding the effects of exoskeleton-assisted walking on gait in healthy individuals.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy adults aged 19-25 years
  • No history of musculoskeletal or neurological disorders
  • Ability to walk independently

Exclusion criteria

  • Any current injury affecting gait
  • Neurological or orthopedic conditions
  • Contraindications to exoskeleton use

Treatment and study plan

Ekso NR Exoskeleton

Device

A wearable robotic exoskeleton used to assist walking during a supervised 30-minute session.

Primary outcomes

  1. Change in plantar pressure distribution

    Time frame: Immediately before and immediately after intervention

    Assessment of plantar pressure parameters measured using a baropodometric platform before and immediately after exoskeleton-assisted walking [kg/cm^2].

Secondary outcomes

  1. Change in spatiotemporal gait parameter

    Time frame: Immediately before and immediately after intervention

    Evaluation of step length [m]

Other outcomes

  1. Change in symmetry

    Time frame: Immediately before and immediately after intervention

    Change in symmetry [%] using baropodometric analysis

Study contacts

Contact information is provided by the study sponsor or research team.

Sebastian Glowinski, Professor

CONTACT

[email protected]

502 684 794 ext. +48

Sponsors and collaborators

Lead sponsor

The State Academy of Applied Sciences in Koszalin

Other

Registry information

Official study title

Immediate Effects of a Single Session of Exoskeleton-Assisted Walking on Plantar Pressure Distribution and Gait Parameters in Healthy Young Adults

Acronym: EKSO-GAIT

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Mar 30, 2026
Registry last updated
Mar 30, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.