Connecting Smartphones With Electronic Health Record to Facilitate Behavioral Goal Monitoring in Diabetes Care
NCT ID: NCT02664233
Last Updated: 2016-11-01
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
EARLY_PHASE1
60 participants
INTERVENTIONAL
2015-06-30
2016-08-31
Brief Summary
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Detailed Description
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Specific Aim 2: To 2a) conduct usability testing and 2b) examine efficacy of this connected interface technology in a 3-month randomized clinical trial in 60 overweight or obese patients with type 2 diabetes in Houston, Texas and Pittsburgh, Pennsylvania.
Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Connected group
Patients will use a smart phone and a fitness tracker for self-monitoring of diet and physical activity for 3 months; 3) Smart phones will provide feedback with graphical presentation of self-monitored information to patients; 4) Patient self-monitored information will be integrated into Chronicle Diabetes, so that educators will be able to view this information and give feedback in a follow-up visit.
Mobile and connected health
Patients will use a smart phone and a fitness tracker for self-monitoring of diet and physical activity for 3 months; 3) Smart phones will provide feedback with graphical presentation of self-monitored information to patients; 4) Patient self-monitored information will be integrated into Chronicle Diabetes, so that educators will be able to view this information and give feedback in a follow-up visit.
Usual diabetes education and care
Participants will receive standard diabetes education and care; each of the recruiting clinics offers diabetes self-management education programs.
No interventions assigned to this group
Interventions
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Mobile and connected health
Patients will use a smart phone and a fitness tracker for self-monitoring of diet and physical activity for 3 months; 3) Smart phones will provide feedback with graphical presentation of self-monitored information to patients; 4) Patient self-monitored information will be integrated into Chronicle Diabetes, so that educators will be able to view this information and give feedback in a follow-up visit.
Eligibility Criteria
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Inclusion Criteria
2. Overweight or obese with an BMI \> 25
3. Able to read and write English
4. Own a smart phone that is Jawbone compatible
Exclusion Criteria
18 Years
ALL
No
Sponsors
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University of Pittsburgh
OTHER
The University of Texas Health Science Center, Houston
OTHER
Responsible Party
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Jing Wang
Associate Professor
Principal Investigators
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Jing Wang, PhD, MPH, RN
Role: PRINCIPAL_INVESTIGATOR
The University of Texas Health Science Center at Houston, School of Nursing
Locations
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University of Pittsburgh
Pittsburgh, Pennsylvania, United States
The University of Texas Health Science Center at Houston
Houston, Texas, United States
Countries
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References
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Wang J, Coleman DC, Kanter J, Ummer B, Siminerio L. Connecting Smartphone and Wearable Fitness Tracker Data with a Nationally Used Electronic Health Record System for Diabetes Education to Facilitate Behavioral Goal Monitoring in Diabetes Care: Protocol for a Pragmatic Multi-Site Randomized Trial. JMIR Res Protoc. 2018 Apr 2;7(4):e10009. doi: 10.2196/10009.
Other Identifiers
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HSC-SN-14-1027
Identifier Type: OTHER
Identifier Source: secondary_id
HSC-SN-14-1027
Identifier Type: -
Identifier Source: org_study_id