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Personalized Smartphone-assisted Coaching System to Improve Glucose Homeostasis in Adults With Prediabetes

Primary Purpose

Prediabetes, Hyperglycemia, Postprandial Hyperglycemia

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Sweetch App + DBWS
Sweetch App Alone
Sponsored by
Johns Hopkins University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Prediabetes focused on measuring Mobile Health

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adults aged 18 -75 years with prediabetes (fasting BG 100-125 mg/dl, A1C 5.7% - 6.4%, or 2 hour BG of 140-199 mg/dl following 75-gram oral glucose tolerance test)
  • Body mass index 24 - 40 kg/m2
  • English speaker
  • Smartphone user (Android or Apple 5s and above)

Exclusion Criteria:

  • Currently doing more than 150 minutes/week of moderate/vigorous physical activity
  • Presence of medical conditions that prevent adoption of moderate physical activity
  • Use of any glucose-lowering or weight loss medications within the previous 3 months
  • Current pregnancy (self-reported) or planning pregnancy during study period (self-reported)
  • Presence of any condition that can result in spurious A1C readings (e.g. anemia [hemoglobin level below lower limit of normal] secondary to iron, vitamin B12, or folate deficiencies; hemoglobinopathies)
  • Use of systemic glucocorticoids
  • Use of antipsychotic medications (stable doses for at least three months of anti-depressants or anti-anxiety drugs will be allowed)
  • Severe mental illness or learning disability
  • Current participation in another clinical trial
  • Liver enzymes >3 x upper limit of normal
  • Poor literacy (REALM-R score of 6 or less)

Sites / Locations

  • Johns Hopkins Hospital
  • Reading Health System

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Sweetch App + DBWS

Sweetch App Alone

Arm Description

Participants receive usual care for prediabetes management. In addition, participants will be randomized to receive the Sweetch app plus weight monitoring via digital body weight scale (DBWS).

Participants receive usual care for prediabetes management. In addition, participants will be randomized to receive the Sweetch app alone.

Outcomes

Primary Outcome Measures

Yield of Recruitment
Proportion of recruited participants who enroll and complete the 3 month study

Secondary Outcome Measures

Engagement
Proportion of enrolled participants who keep app installed and open in background of their smartphones during duration of the study.
Usability and Satisfaction
Usability and Satisfaction will be measured using an adapted Systems Usability Scale, a validated method of measuring usability with a wide array of technological products, including smartphones.
Adherence to physical activity goal
Proportion of enrolled participants meeting mean 150 minute per week physical activity target (evaluated at 4 week intervals and over course of entire 12 week study period)

Full Information

First Posted
August 1, 2016
Last Updated
March 26, 2018
Sponsor
Johns Hopkins University
Collaborators
Sweetch Health, Ltd
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1. Study Identification

Unique Protocol Identification Number
NCT02896010
Brief Title
Personalized Smartphone-assisted Coaching System to Improve Glucose Homeostasis in Adults With Prediabetes
Official Title
Effectiveness of a Personalized Smartphone-assisted Coaching System to Improve Glucose Homeostasis in Adults With Prediabetes: Rationale and Study Protocol - Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Completed
Study Start Date
October 10, 2016 (Actual)
Primary Completion Date
November 17, 2017 (Actual)
Study Completion Date
November 17, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins University
Collaborators
Sweetch Health, Ltd

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Sweetch is a personalized mobile-health platform coaching system (mobile phone app) designed to promote adherence to physical activity guidelines for people with prediabetes.
Detailed Description
The mobile phone app Sweetch seeks to increase leisure time physical activity rather than formal exercise through the use of a behavioral analytics engine that continuously process various aspects of the user's life habits, taking into account the user's demographics, behavioral change status, schedule, actual activity patterns, and more. The rationale behind this approach is that long-term adherence and patient engagement are more likely to be achieved when demands on manual user data entry are kept at a minimum. Compared to similar smartphone-assisted prevention apps, there are two novel features of the Sweetch app that may increase its efficacy. First, it uses a "just-in-time" adaptive intervention" approach that tailors recommendations to the user's day-to-day routine and his or her readiness for behavioral change. Second, and most importantly, it requires no direct involvement by the user, since all the necessary data is collected using built-in tracking pedometers, accelerometer and GPS (Global Positioning System) sensors on smartphones. In contrast, interventions that focus on dietary changes (i.e. calorie reduction, change in macronutrient content), require active user tracking at every meal, which is difficult to maintain in the long-term even with the use of sophisticated, electronic calorie counting tools. For these reasons, the Sweetch app may achieve greater long-term adherence, which is usually a limiting factor to efficacy of mobile health interventions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prediabetes, Hyperglycemia, Postprandial Hyperglycemia, Impaired Glucose Tolerance, Impaired Fasting Glucose
Keywords
Mobile Health

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
55 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sweetch App + DBWS
Arm Type
Active Comparator
Arm Description
Participants receive usual care for prediabetes management. In addition, participants will be randomized to receive the Sweetch app plus weight monitoring via digital body weight scale (DBWS).
Arm Title
Sweetch App Alone
Arm Type
Active Comparator
Arm Description
Participants receive usual care for prediabetes management. In addition, participants will be randomized to receive the Sweetch app alone.
Intervention Type
Other
Intervention Name(s)
Sweetch App + DBWS
Intervention Description
Usual care for prediabetes management, Sweetch app, weight monitoring via digital body weight scale (DBWS).
Intervention Type
Other
Intervention Name(s)
Sweetch App Alone
Intervention Description
Usual care for prediabetes management, Sweetch app alone.
Primary Outcome Measure Information:
Title
Yield of Recruitment
Description
Proportion of recruited participants who enroll and complete the 3 month study
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Engagement
Description
Proportion of enrolled participants who keep app installed and open in background of their smartphones during duration of the study.
Time Frame
3 months
Title
Usability and Satisfaction
Description
Usability and Satisfaction will be measured using an adapted Systems Usability Scale, a validated method of measuring usability with a wide array of technological products, including smartphones.
Time Frame
3 months
Title
Adherence to physical activity goal
Description
Proportion of enrolled participants meeting mean 150 minute per week physical activity target (evaluated at 4 week intervals and over course of entire 12 week study period)
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults aged 18 -75 years with prediabetes (fasting BG 100-125 mg/dl, A1C 5.7% - 6.4%, or 2 hour BG of 140-199 mg/dl following 75-gram oral glucose tolerance test) Body mass index 24 - 40 kg/m2 English speaker Smartphone user (Android or Apple 5s and above) Exclusion Criteria: Currently doing more than 150 minutes/week of moderate/vigorous physical activity Presence of medical conditions that prevent adoption of moderate physical activity Use of any glucose-lowering or weight loss medications within the previous 3 months Current pregnancy (self-reported) or planning pregnancy during study period (self-reported) Presence of any condition that can result in spurious A1C readings (e.g. anemia [hemoglobin level below lower limit of normal] secondary to iron, vitamin B12, or folate deficiencies; hemoglobinopathies) Use of systemic glucocorticoids Use of antipsychotic medications (stable doses for at least three months of anti-depressants or anti-anxiety drugs will be allowed) Severe mental illness or learning disability Current participation in another clinical trial Liver enzymes >3 x upper limit of normal Poor literacy (REALM-R score of 6 or less)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nestoras Mathioudakis, MD MHS
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Adrian S Dobs, MD MHS
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Johns Hopkins Hospital
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21287
Country
United States
Facility Name
Reading Health System
City
Reading
State/Province
Pennsylvania
ZIP/Postal Code
19607
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
29487046
Citation
Everett E, Kane B, Yoo A, Dobs A, Mathioudakis N. A Novel Approach for Fully Automated, Personalized Health Coaching for Adults with Prediabetes: Pilot Clinical Trial. J Med Internet Res. 2018 Feb 27;20(2):e72. doi: 10.2196/jmir.9723.
Results Reference
derived

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Personalized Smartphone-assisted Coaching System to Improve Glucose Homeostasis in Adults With Prediabetes

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