prevesc0001: A Wireless Lingual Feedback Device to Reduce Overpressures in Seated Posture: A Feasibility Study

Sponsor
TIMC-IMAG (Other)
Overall Status
Completed
CT.gov ID
NCT00917228
Collaborator
Olivier Chenu (Other), Nicolas Vuillerme (Other), Jacques Demongeot (Other), Yohan Payan (Other)
1

Study Details

Study Description

Brief Summary

This study evaluates the feasibility of a biofeedback system aimed at reducing overpressures during seated posture. The system consists of (1) a pressure sensors map, (2) a laptop that couples sensors with actuators, (3) a Tongue Display Unit (TDU) consisting of a wireless circuit embedded in a dental retainer with a matrix of electrodes. The principle of this biofeedback system consists in (1) detecting overpressures in people who are seated over long periods of time, (2) estimating a postural change that could reduce these overpressures and (3) communicating this change through directional information transmitted by the TDU.

It is hypothesized that overpressures are diminished after biofeedback.

Condition or Disease Intervention/Treatment Phase
  • Device: recordings with device equipped
  • Device: Control

Study Design

Study Type:
Observational
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
A Wireless Lingual Feedback Device to Reduce Overpressures in Seated Posture: A Feasibility Study

Arms and Interventions

Arm Intervention/Treatment
Feedback

Subjects of this group are equipped with the biofeedback system

Device: recordings with device equipped

Control

Subjects of this group are not equipped with the biofeedback system

Device: Control
Recording without device equipped

Outcome Measures

Primary Outcome Measures

  1. Ability to reach a target posture [10 seconds]

  2. Decrease of the overpressures at the seat/body interface [10 seconds]

  3. Decrease of overpressures bigger for higher pressures [10 seconds]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 50 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • young healthy subjects
Exclusion Criteria:
  • motor or sensory disabilities

Contacts and Locations

Locations

Site City State Country Postal Code
1 Timc-Imag La tronche France 38710

Sponsors and Collaborators

  • TIMC-IMAG
  • Olivier Chenu
  • Nicolas Vuillerme
  • Jacques Demongeot
  • Yohan Payan

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00917228
Other Study ID Numbers:
  • prevesc0001
First Posted:
Jun 10, 2009
Last Update Posted:
Jun 10, 2009
Last Verified:
Jun 1, 2009

Study Results

No Results Posted as of Jun 10, 2009