Web-Based Intervention Designed to Educate and Improve Adherence Through Learning to Use Continuous Glucose Monitoring
NCT ID: NCT03367351
Last Updated: 2018-12-17
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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COMPLETED
NA
8 participants
INTERVENTIONAL
2018-03-09
2018-11-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Web-Based Educational Intervention
Participants receiving the Web-Based Educational Intervention will be enrolled to the research protocol for six weeks of module-based learning and online discussion sessions and followed for a total of 3-months post CGM implementation to collect study measures.
Web-Based Education
Completion of a CGM specific web-based educational intervention that includes a series of online learning modules.
Social Support
Engagement in peer-led CGM specific discussion boards
Standard of Care
Participants will receive standard clinical care. Similar study measures will be collected to compare between groups.
Standard of Care
Standard of Care - serves as the control group for the treatment arm
Interventions
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Web-Based Education
Completion of a CGM specific web-based educational intervention that includes a series of online learning modules.
Social Support
Engagement in peer-led CGM specific discussion boards
Standard of Care
Standard of Care - serves as the control group for the treatment arm
Eligibility Criteria
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Inclusion Criteria
2. Diagnosed with type 1 diabetes (T1D) for \> 3 months before consent is obtained
3. Aged \>15 years and \<24 years at time of enrollment
4. Must have access to a smartphone, tablet or laptop/desktop computer with high speed internet access and speaker
5. Must be using/initiating a Dexcom CGM
Exclusion Criteria
2. Significant medical comorbidity in the adolescent or young adult that could, in the opinion of the PI, affect subject's capacity to follow study protocol
3. Previous use of a CGM within the last 3 months
4. Unwilling or unlikely to return to clinic for a follow-up HbA1c test
5. Unwillingness to accept randomization
15 Years
24 Years
ALL
No
Sponsors
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University of Florida
OTHER
Responsible Party
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Principal Investigators
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Madison B Smith, BSN, PhD Candidate
Role: PRINCIPAL_INVESTIGATOR
University of Florida
Locations
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University of Florida
Gainesville, Florida, United States
Countries
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References
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Smith MB, Albanese-O'Neill A, Yao Y, Wilkie DJ, Haller MJ, Keenan GM. Feasibility of the Web-Based Intervention Designed to Educate and Improve Adherence Through Learning to Use Continuous Glucose Monitor (IDEAL CGM) Training and Follow-Up Support Intervention: Randomized Controlled Pilot Study. JMIR Diabetes. 2021 Feb 9;6(1):e15410. doi: 10.2196/15410.
Other Identifiers
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IRB201701822
Identifier Type: OTHER
Identifier Source: secondary_id
UFT1DCGM2017
Identifier Type: -
Identifier Source: org_study_id