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

Results pending

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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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

64 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-10-07

Study Completion Date

2026-12-25

Brief Summary

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This project is designed to: a) develop a new test called UHasselt Locomotor Sensory Integration Test (UHLSINT) which would allow us to evaluate sensory interaction process in locomotion assess whether Locomotor CTSIB and to investigate whether UHLSINT is a reliable test to evaluate sensory interaction in both young and older adults, b) evaluate the difference in sensory interaction and balance performance between standing and walking between both young and older adults, c) examine the changes in sensory interaction process under challenging conditions such as perturbations, dual-task, and when both are present between both young and older adults, d) examine the association between overall fall risk defined by the single-large perturbations and sensory interaction processes used during all the trials in both age groups.

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.

Detailed Description

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Conditions

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Healthy Young Adults Older Adults (65 Years and Older) Elderly

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

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

Intervention Type OTHER

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

Intervention Type OTHER

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

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Young adults who: 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, will be invited to participate. Community-dwelling older adults who: a) are 65 years old and over and, b) have not fallen in the last 12 months will also be invited to participate.

Exclusion Criteria

* having had serious lower extremity injuries or operations in the past year,
* 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,
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Hasselt University

OTHER

Sponsor Role lead

Responsible Party

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Pieter Meyns

Assoc. Prof.

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Hasselt University

Diepenbeek, , Belgium

Site Status

Countries

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Belgium

Central Contacts

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Esma Nur Kolbasi Dogan, PhD

Role: CONTACT

+32 11 268050

Other Identifiers

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HasseltU100

Identifier Type: -

Identifier Source: org_study_id

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