Posture Standards of a New Dynamic Platform

NCT ID: NCT05532176

Last Updated: 2025-07-25

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

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

260 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-06-07

Study Completion Date

2026-04-04

Brief Summary

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The objective is the determination of norms on healthy subjects, by age groups (20-29/30-39/40-49/50-59/60-69/70-79/80-89 years) for the posturological evaluation of four posture tests: the sensory organization test, the motor coordination test, the adaptation test, the stability limit test.

Detailed Description

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The objective is the determination of norms by age groups (20-29/30-39/40-49/50-59/60-69/70-79/80-89) of four tests of posture: the test of sensory organization, the test of motor coordination, the test of adaptation, the test of stability limit, of a new platform of static and dynamic posturology.

When moving within an environment, sensory information from the environment and the body is registered within the sensory systems (Hilber et al., 2018). More specifically, it is the functions of balancing and spatial orientation that are brought into play to produce behavioral responses that are adapted to different situations and to anticipate events in one's environment. It is therefore essential to establish not only posturological norms but also norms for the function of spatial orientation in order to propose a complete assessment of the postural and spatial cognitive profile of healthy subjects that can serve as a reference population.

These standards will serve as a basis for determining the pathological values during the exploration of numerous pathologies, in particular vestibular pathology, pathologies inducing balance and posture disorders (neurology, rheumatology).

The measurement of posture and variations of the center of gravity represents an important output marker, little or never taken into account in medical practice, and linked to a large number of integration processes, in particular multisensory and sensory-motor. Its parameters vary according to the sensory information received and processed related to the maintenance of balance: visual system, vestibular system, somesthesic system, visceral sensory system. Posture is also modulated by the attentional level and cognitive load. Posturography is one of the most cost-effective instruments in terms of clinical utility, particularly in the diagnosis of vestibular pathology (Stewart et al., 1999). Thus, the development of such an instrument represents an innovative and advantageous development in terms of diagnostic improvement.

the investigators will perform the standard setting according to a precise statistical approach (analysis of variance ANOVA with correlation coefficients and 95% confidence intervals to establish test-retest reliability).

Conditions

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Static and Dynamic Posture Standards

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

seven sub-groups of 40 persons each according to their age: 20-29/30-39/40-49/50-59/60-69/70-79/80-89years old
Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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postural group

one healthy group of different age

Group Type OTHER

Posture standards

Intervention Type OTHER

Dynamic and static Postural measurements according to four types of tests

Interventions

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Posture standards

Dynamic and static Postural measurements according to four types of tests

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* No symptoms of vertigo, dizziness, balance disorders, motion sickness;
* No history of neurological or musculoskeletal pathology;
* No history of neurological or musculoskeletal pathology; -No known medication or medication likely to modify balance;
* No history of two or more falls in the six months preceding the study;
* No psychiatric disorder;
* Normal vision with or without correction;
* Be able to stand for more than 20 minutes and walk independently

Exclusion Criteria

* Subjects under 20 years of age
* Pregnant or breastfeeding women,
* Persons in an emergency situation or unable to give their consent, including adults under guardianship
* Persons under legal protection
* Persons deprived of liberty, minors, protected adults,
* Inclusion of the subject in another interventional research protocol with pharmacological objectives during the present study
Minimum Eligible Age

20 Years

Maximum Eligible Age

89 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University Hospital, Caen

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Caen University Hospital

Caen, , France

Site Status

Countries

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France

Other Identifiers

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2022-A00856-37

Identifier Type: -

Identifier Source: org_study_id

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