Effect of Exoskeleton-Assisted Walking on Gait Parameters in Healthy Adults
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Ekso NR Exoskeleton.
- Who it may be relevant to
- Registry conditions: Gait Analysis in Healthy Subjects. Basic parameters: 19 years — 25 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Immediate Effects of a Single Session of Exoskeleton-Assisted Walking on Plantar Pressure Distribution and Gait Parameters in Healthy Young Adults
Overview
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.
Detailed description
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.
Interventions
- Device Ekso NR Exoskeleton
A wearable robotic exoskeleton used to assist walking during a supervised 30-minute session.
Primary outcome measures
- Change in plantar pressure distribution [Time frame: Immediately before and immediately after intervention]
Secondary outcome measures (1)
- Change in spatiotemporal gait parameter [Time frame: Immediately before and immediately after intervention]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Basic science
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07499063 · EKSO_GAIT_2026_01