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Human Factors and Home Use Study of the Vigilant Diabetes Management Application

NCT02276131 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 61

Last updated 2016-02-24

No results posted yet for this study

Summary

A human factors and home use study to assess whether subjects with diabetes and their caregivers can understand feedback received from the Vigilant Diabetes Management Application about their blood glucose patterns and whether the decisions made in response to device feedback are made in accordance with the intended use.

Conditions

Interventions

DEVICE

Vigilant Diabetes Management Application

Human factors and usability assessment of the device in the hands of diabetes subjects and caregivers

Sponsors & Collaborators

  • University of Virginia

    collaborator OTHER

  • InSpark Technologies, Inc.

    lead INDUSTRY

Principal Investigators

  • Stacey Anderson, MD · University of Virginia

Study Design

Allocation
NA
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
13 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-01-31
Primary Completion
2015-09-30
Completion
2015-12-31

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Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02276131 on ClinicalTrials.gov