Sensory Interaction and Balance Control During Standing and Walking in Healthy Young and Older Adults
NCT ID: NCT06629922
Last Updated: 2024-10-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
64 participants
OBSERVATIONAL
2024-10-07
2026-12-25
Brief Summary
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In order to achieve these aims, 10 trials will be conducted:
Trial 1- Single-Large Perturbation in Standing Trial 2- Single-Large Perturbation in Walking Trial 3- Instrumented CTSIB Trial 4- Locomotor CTSIB Trial 5- Instrumented CTSIB + Perturbations Trial 6- Locomotor CTSIB + Perturbations Trial 7- Instrumented CTSIB + Auditory Stroop Test Trial 8- Locomotor CTSIB + Auditory Stroop Test Trial 9- Instrumented CTSIB + Perturbations + Auditory Stroop Test Trial 10- Locomotor CTSIB + Perturbations + Auditory Stroop Test
Two different treadmill perturbations will be applied in addition to the Instrumented CTSIB and UHLSINT: a) slip perturbations, b) continuous perturbations. An auditory stroop task will be applied in relevant trials.
All of the trials will be performed in CAREN High-End Systems (Motek Medical BV, Amsterdam, The Netherlands) which is a motion capture system that is equipped with a treadmill mounted on a 6 degree of freedom motion base, a 360ยบ dome-shaped virtual reality (VR) screen, and a marker-based movement analysis system.
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Young Adults
a) aged between 18 to 35 years old and, b) have never been diagnosed with somatosensory, visual, and vestibular deficits as reported by the participants
No intervention
This is a observational study and the participants will not receive any intervention
Older Adults
a) are 65 years old and over and, b) have not fallen in the last 12 months will also be invited to participate
No intervention
This is a observational study and the participants will not receive any intervention
Interventions
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No intervention
This is a observational study and the participants will not receive any intervention
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* having any neurological (stroke, epilepsy, Parkinson's disease, etc.), sensory (i.e. peripheral neuropathy, diminished sense of pain, etc.) or motor disorder that can interfere with the results of the study
* Diagnosed vascular, respiratory, cardiac, orthopedic, or other disorders that affect the subject's ability to exercise safely,
18 Years
ALL
Yes
Sponsors
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Hasselt University
OTHER
Responsible Party
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Pieter Meyns
Assoc. Prof.
Locations
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Hasselt University
Diepenbeek, , Belgium
Countries
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Central Contacts
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Other Identifiers
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HasseltU100
Identifier Type: -
Identifier Source: org_study_id
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