Characterization of Sitting Postures in Healthy Subjects

NCT ID: NCT01857089

Last Updated: 2014-04-11

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

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-05-31

Study Completion Date

2013-08-31

Brief Summary

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The aim of this study is to assess the intra and inter-subjects variability of the pressure measurement cartography in healthy and well and able volunteers, sitting on a rigid base during two hours.

Detailed Description

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* The purpose of this study is to understand the formation of pressure sore, to improve the care of paraplegic patients.
* This pilot study is going to help to establish a model in healthy volunteers in the prevention of pressure sores.

Conditions

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Pressure Ulcer

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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Pressure Measurement

Group Type EXPERIMENTAL

Orthotest CE

Intervention Type DEVICE

Orthotest CE is a rigid base mapping system composed by 1024 pressure transducers uniformly distributed in a 35x35 cm surface.

Orthotest CE is a product manufactured by Vista-Medical. The patient sit on the rigid base during 2 hours to record the pressure and all the data needed for the pilot study.

Pressure measurement

Interventions

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Orthotest CE

Orthotest CE is a rigid base mapping system composed by 1024 pressure transducers uniformly distributed in a 35x35 cm surface.

Orthotest CE is a product manufactured by Vista-Medical. The patient sit on the rigid base during 2 hours to record the pressure and all the data needed for the pilot study.

Pressure measurement

Intervention Type DEVICE

Other Intervention Names

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Orthotest CE mark Vista-Medical Mapping system

Eligibility Criteria

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Inclusion Criteria

* more or equal than 18 years old
* age between 20 and 30 years old
* affiliation to social security or similarly regime

Exclusion Criteria

* Person with pacemaker
* Person with a history of lumbar pain, chest or/and cervical pain.
* Person with an history of lumbar, chest or/and cervical muscular disorders,
* Person with history of circulatory problems,
* Person with history of skin pathologies at the seat area,
* Protected person referred to in Articles L1121-5 to L1121-8 of the Code of Public Health
* Person having a total annual compensation for the participation in biomedical research higher than €4460.
Minimum Eligible Age

20 Years

Maximum Eligible Age

30 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University Hospital, Grenoble

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Alexandre MOREAU-GAUDRY, MD,PhD

Role: PRINCIPAL_INVESTIGATOR

INSERM-CIC-IT

Locations

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CIC-IT GrenobleUniversityHospital

Grenoble, , France

Site Status

Countries

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France

Related Links

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Other Identifiers

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CaPAS-DCIC-1204

Identifier Type: -

Identifier Source: org_study_id

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