The Passy Muir Swallowing Self Training Device

CompletedOBSERVATIONAL
Enrollment

13

Participants

Timeline

Start Date

January 1, 2013

Primary Completion Date

February 22, 2016

Study Completion Date

February 22, 2016

Conditions
Oropharyngeal Dysphagia
Interventions
DEVICE

Vibrotactile stimulation

Comparison of the effects of different vibratory characteristics on the frequency of swallowing, time of initiation of swallowing with stimulation and urge to swallow. Will compare frequency of vibration, mode of vibration, pressure of device against neck, and duration of vibration. Each session will last no more than 1 hour with short breaks. Each participant can volunteer for up to three nonconsecutive sessions.

Trial Locations (1)

22801

James Madison University and Rockingham Memorial Hospital, Harrisonburg

All Listed Sponsors
collaborator

Passy Muir Inc.

INDUSTRY

lead

James Madison University

OTHER

NCT01765673 - The Passy Muir Swallowing Self Training Device | Biotech Hunter | Biotech Hunter