- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00923975
Evaluation of DIDGET TM World Reports
Evaluation of Avatar Web Reports
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
California
-
Escondido, California, United States, 92026
- AMCR Institute
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Lay users must be:
- Be at least 18 years of age
- Have diabetes or be the parent or legal guardian of a child with diabetes
- Be testing blood sugar at home at least twice daily for at least one month or be the parent or legal guardian of a child who has been testing blood sugar at home at least twice daily for at least one month
- Be able to speak, read, and understand English
- Have experience using a PC, navigating software programs, or browsing the internet
Healthcare professionals must:
- Have experience using the internet
- Have experience using diabetes data management software in the medical office
Exclusion Criteria:
- Person working for a competitive medical device company
- Person having a cognitive disorder or condition which, in the opinion of the investigator, would put the person at risk or compromise the integrity of the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Intended Users of the Software
Young adults, parents/guardians of young people under age 18, and healthcare professionals who work with this population would be intended users of the data management program.
The DIDGET World Reports software is used to upload blood glucose results from the DIDGET Blood Glucose Monitoring System so that intended users can identify patterns in their diabetes management.
|
During the study subjects performed specific tasks, such as uploading meter results to a secure website and displaying reports.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of Participants Who Rated Successful (<=3) by Healthcare Professionals When Participants Performed Specific Software Tasks
Time Frame: 1-2 hours
|
Study staff rated participants on their success at performing specific tasks. The rating scale was:
|
1-2 hours
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of Participants Who Rated Clarity and Usefulness of User Instructions as Good to Excellent (>=3)
Time Frame: 1-2 hours
|
After the software evaluation, subjects were asked to review the online help and rate it on a 5 point scale.
|
1-2 hours
|
|
Number of Participants Who Rated Ease of Performing Specific Tasks as Very Simple to Neither Simple Nor Difficult (<=3 Rating)
Time Frame: 1-2 hours
|
Subjects rated ease of using the software with respect to specific tasks. The rating scale was:
|
1-2 hours
|
|
Number of Participants Who Rated Their Satisfaction With The Following as Good to Excellent (>=3)
Time Frame: 1-2 hours
|
Subjects responded to questionnaires in rating features and appearance, usefulness, and satisfaction on a 5 point scale:
|
1-2 hours
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Timothy Bailey, MD, AMCR Institute
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- CTD-2009-08
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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