Sensory Re-training following Orthognathic Surgery
Project Number5R01DE013967-04
Contact PI/Project LeaderPHILLIPS, CEIB
Awardee OrganizationUNIV OF NORTH CAROLINA CHAPEL HILL
Description
Abstract Text
DESCRIPTION: (provided by the applicant) Abnormal facial sensation has a
negative impact on patient's oral behaviors and may adversely affect a
patient's quality of life if the altered sensation persists. Many patients with
abnormal sensations retain some sensory function and do not develop chronic
pain, and for those individuals there are no currently evidence-based
noninvasive therapies. The goal of this project is to evaluate sensory
re-training, a rehabilitative therapy that offers significant potential for
patients who experience impaired sensory function regardless of the cause. This
behavior therapy approach has been used with substantial clinical success with
hand injury patients since the 1970s. Re-training appears to enhance central
reorganization of the impulses from an injured sensory nerve to the cerebral
cortex so that the altered sensory signals can be interpreted and translated
into functionally meaningful motor functions.
Sensory re-training will be compared to a placebo jaw-opening exercise in a
single blind, randomized two-arm parallel group stratified block clinical
trial, using orthognathic surgery patients as subjects. Orthognathic surgery
patients offer an uncompromised model for the evaluation of new rehabilitative
therapies. These healthy patients, treated to correct dentofacial deformity,
present for surgery with no neurosensory impairment, but yet routinely
experience substantial alterations in facial sensation following the surgical
procedure. The effcts of sensory re-training will be evaluated using three
types of outcomes: patient-centered measures to assess the magnitude of the
negative effect of altered sensation after surgery and the recovery time needed
to reach little or no negative effect; neurosensory behavior measures to assess
the patient's ability to learn alternate cues for touch perception and
discrimination; and a conventional neurosensory contact threshold measure to
assess the actual deficit. Our primary focus will be on the patient's
perception of the negative impact of altered sensation on daily life.
National Institute of Dental and Craniofacial Research
CFDA Code
121
DUNS Number
608195277
UEI
D3LHU66KBLD5
Project Start Date
15-July-2001
Project End Date
31-May-2006
Budget Start Date
01-June-2004
Budget End Date
31-May-2005
Project Funding Information for 2004
Total Funding
$345,563
Direct Costs
$267,449
Indirect Costs
$121,690
Year
Funding IC
FY Total Cost by IC
2004
National Institute of Dental and Craniofacial Research
$345,563
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5R01DE013967-04
Publications
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Outcomes
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Clinical Studies
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