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Real-Time Internet Evaluation of Swallowing

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University of Arkansas

Status

Completed

Conditions

Stroke
Head and Neck Cancer

Study type

Observational

Funder types

Other

Identifiers

NCT00580138
1R01DC005603 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The purpose of this study is to determine whether real-time internet evaluations of swallowing, or x-ray swallow studies viewed over closed internet circuit, are a reliable method of evaluating swallowing function.

Full description

The objective of this proposal is to establish the validity of an Internet based protocol for real-time, remote, telefluoroscopic evaluation of oropharyngeal swallowing function. The investigators will achieve this goal by testing the hypothesis that oropharyngeal swallowing function evaluated by an experienced speech-language pathologist (SLP) using a remote, interactive, real-time, dynamic Internet telefluoroscopic procedure, which was developed in the PI's laboratory, has an acceptable level of agreement with the evaluations performed by an experienced SLP who is present in the fluoroscopy suite and using the traditional videofluoroscopic methodology. In other words, the primary aim of this investigation is to determine whether the telemedicine approach to evaluation of swallowing function is reliable relative to the traditional method by which a clinician is in direct contact with a patient for a pre-examination interview, clinical examination, and videofluoroscopic evaluation of swallowing function. Confirmation of the reliability of the telefluoroscopic evaluation of oropharyngeal dysphagia (hereafter referred to as dysphagia) can result in equity of access for underserved groups for whom SLPs with expertise in evaluating swallowing function are locally unavailable. Ultimately, the success of this project could translate specialty services into routine clinical practice across the United States and globally.

Enrollment

30 patients

Sex

All

Ages

21+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Stroke, Head & neck cancer, referred for swallowing evaluation.

Exclusion criteria

  • No stroke or no head and neck cancer, or not referred for swallowing evaluation.

Trial design

30 participants in 1 patient group

Stroke or Head & Neck Cancer
Description:
Any subject who has suffered a stroke or has some form of head \& neck cancer (non-laryngectomee) may be enrolled.

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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