Accuracy of Blood Glucose Detection by Diabetes Alert Dogs
NCT ID: NCT02126605
Last Updated: 2014-04-30
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
16 participants
OBSERVATIONAL
2014-07-31
2015-03-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* The participant must have a DAD placed in their home for a minimum of 6 months.
* Participants must not currently be using a continuous glucose monitor (CGM) in their diabetes management.
* Participants must be capable of performing all tasks involved in the study protocol, including filling out questionnaires and diaries in English.
* Participants must have an internet-connected computer compatible with study software.
* Willingness to avoid consumption of acetaminophen-containing products for the duration of the study.
Exclusion Criteria
* Current use of a CGM
* History of a systemic deep tissue infection with methicillin-resistant staph aureus or Candida albicans
6 Years
65 Years
ALL
No
Sponsors
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University of Virginia
OTHER
Responsible Party
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Linda Gonder-Frederick
Associate Professor
Principal Investigators
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Linda Gonder-Frederick, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
University of Virginia
Locations
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University of Virginia Center for Behavioral Medicine Research
Charlottesville, Virginia, United States
Countries
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Central Contacts
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Facility Contacts
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Jesse Grabman, B.A.
Role: primary
Other Identifiers
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17296
Identifier Type: -
Identifier Source: org_study_id