Real-Time Internet Evaluation of Swallowing

This study has been completed.

Study NCT00580138 Information provided by University of Arkansas

First Received on December 20, 2007. Last Updated on May 6, 2010 History of Changes

Results First Received: May 6, 2010

Study Type:	Observational
Study Design:	Observational Model: Case-Only; Time Perspective: Prospective
Condition:	Stroke and/or Head and Neck Cancer.

Participant Flow

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Recruitment Details

Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
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Pre-Assignment Details

Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
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Reporting Groups

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

Participant Flow: Overall Study

	Stroke or Head & Neck Cancer
STARTED	30
COMPLETED	30
NOT COMPLETED	0

Baseline Characteristics

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Reporting Groups

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

Baseline Measures

	Stroke or Head & Neck Cancer
Number of Participants [units: participants]	30
Age [units: participants]
<=18 years	0
Between 18 and 65 years	19
>=65 years	11
Age [units: years] Mean ± Standard Deviation	62 ± 4
Gender [units: participants]
Female	13
Male	17
Region of Enrollment [units: participants]
United States	30

Outcome Measures

1. Primary:

Reliability Ratings Among Clinicians Using Real-time Internet Evaluation of Swallowing. [ Time Frame: 2 years ]

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Serious Adverse Events

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Other Adverse Events

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More Information

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Certain Agreements:

Principal Investigators are NOT employed by the organization sponsoring the study.

There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.

Limitations and Caveats

Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data
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Results Point of Contact:

Name/Title: Gary McCullough
Organization: University of Arkansas for Medical Sciences Medical Center
phone: 501-852-7886
e-mail: mcculloughgaryh@uams.edu

No publications provided

Responsible Party:	Adrienne Perlman, University of Illinois, Urbana-Champaign
ClinicalTrials.gov Identifier:	NCT00580138 History of Changes
Other Study ID Numbers:	1 R01 DC005603, 1 R01 DC005603
Study First Received:	December 20, 2007
Results First Received:	May 6, 2010
Last Updated:	May 6, 2010
Health Authority:	United States: Institutional Review Board