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A Novel Carbohydrate Counting Smartphone App for Youth With Type 1 Diabetes

Primary Purpose

Diabetes Mellitus, Type 1

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
iSpy
Sponsored by
The Hospital for Sick Children
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Diabetes Mellitus, Type 1

Eligibility Criteria

10 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosed with T1DM for ≥6 months;
  • Completion of initial carbohydrate counting classes;
  • Incorporating carbohydrate counting into treatment regimen;
  • Having access to a smart phone and data plan;

Exclusion Criteria:

  • Cognitive impairments or co-morbid physical or psychiatric condition (e.g. blindness, clinical depression, anxiety disorder) that might impact ability to use iSpy;
  • Diagnosis of condition that affects dietary exposure (e.g. celiac disease);
  • Participation in usability study;

Sites / Locations

  • The Hospital for Sick Children

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

iSpy

Control

Arm Description

In addition to usual care, participants in the intervention group will receive the iSpy intervention.

The control group participants will continue to use their usual method of carbohydrate counting for a 3-month period.

Outcomes

Primary Outcome Measures

Carbohydrate (CHO) Counting Accuracy
Assessing CHO counting using 10 food items from all major food groups. For each group, a simple food (e.g. an apple) and complex food (e.g. food with 2+ components but base food from targeted group) is included. A Co-investigator, Registered Dietitian (RD)/Certified Diabetes Educator (CDE), selected 2 sets of 10 food items for the study visits (verified that both sets were similar difficulty). The net CHO value (true value) for each food will be based on the nutrition label, USDA Nutrient Database (Release 28), Canadian Nutrient File, or by RD/CDE. For each food, data will be obtained from all participants: • Estimated net CHO (in grams) And with the above data, the following will be calculated: % of food for which subjects estimated the CHO content within (+/-) 10 grams of true value. Change (%) in the above accuracy measure for counting at baseline versus 3-month follow-up visit in iSpy vs control groups.
Carbohydrate (CHO) Counting Efficiency (Time to count)
Assessing CHO counting using 10 food items from all major food groups. For each group, a simple food (e.g. an apple) and complex food (e.g. food with 2+ components but base food from targeted group) is included. A Co-investigator, Registered Dietitian (RD)/Certified Diabetes Educator (CDE), selected 2 sets of 10 food items for the study visits (verified that both sets were similar difficulty). The net CHO value (true value) for each food will be based on the nutrition label, USDA Nutrient Database (Release 28), Canadian Nutrient File, or by RD/CDE. For each food, data will be obtained from all participants: • Time required to estimate net CHO (in seconds) In order to calculate the following: • Change in the above time taken for counting at baseline versus 3-month follow-up visit in iSpy vs control groups.

Secondary Outcome Measures

Change in Quality of Life: Self Care Inventory Questionnaire
Quality of Life questionnaires will be analyzed for any change from baseline to 3-month follow-up within both the intervention and control groups. The first questionnaire including: • Self Care Inventory: Scale from 1 (Never do it) to 5 (Always do this as recommended without fail);
Change in Quality of Life: Diabetes Questionnaire
Quality of Life questionnaires will be analyzed for any change from baseline to 3-month follow-up within both the intervention and control groups. The second questionnaire including: • Diabetes Family Responsibility Questionnaire: Selection of 1 of 3 statements best describing the way each task is handled in the family from 1 (Parent taking responsibility almost all of the time) 2 (Parent and Child sharing responsibility equally) to 3 (Child taking responsibility almost all of the time);
Change in Quality of Life: Quality of Life for Youth
Quality of Life questionnaires will be analyzed for any change from baseline to 3-month follow-up within both the intervention and control groups. The third questionnaire including: • Quality of Life for Youth: Scale from 0 (Never) to 4 (All the time);
Change in Quality of Life: Global Quality of Life
Quality of Life questionnaires will be analyzed for any change from baseline to 3-month follow-up within both the intervention and control groups. The last questionnaire including: • Global Quality of Life: Scale from 1 (No Change) to 7 (A great deal better);
Implementation outcomes: Accrual/Attrition Rates
• Criteria for implementation success will be based on the studies previously conducted by Co-Principal Investigator (JS): Participant accrual (total completed / total enrolled) and attrition rates (total dropouts / total enrolled). Success being defined as accrual rates >70% and attrition rates <15%;
Implementation outcomes: Engagement
• Levels of engagement will be assessed as follows: Low: defined as less than 1 logged meal every 2 weeks High: defined as greater than 1 logged meal every 2 weeks.
Implementation outcomes: Acceptability
• Acceptability: 7 item Acceptability e-Scale (AES) regarding level of acceptability from a scale of 1 (low) to 5 (high) of iSpy, with high acceptability being item mean score of 4 on AES. 2 additional qualitative items are included in AES and will be evaluated.

Full Information

First Posted
April 10, 2020
Last Updated
April 16, 2020
Sponsor
The Hospital for Sick Children
Collaborators
The Physicians' Services Incorporated Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT04354142
Brief Title
A Novel Carbohydrate Counting Smartphone App for Youth With Type 1 Diabetes
Official Title
iSpy: A Pilot Randomized Control Trial of a Novel Carbohydrate Counting Smartphone App for Youth With Type 1 Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
July 12, 2018 (Actual)
Primary Completion Date
January 27, 2020 (Actual)
Study Completion Date
January 27, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Hospital for Sick Children
Collaborators
The Physicians' Services Incorporated Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Type 1 Diabetes Mellitus (T1DM) is a common chronic disease of childhood. T1DM has substantial impact on quality of life (QOL), including burdensome dietary restrictions and the need to count carbohydrates in foods to safely dose insulin. Carbohydrate counting is challenging, inconvenient, and, if done wrong, can cause high or low blood glucose levels. To address these challenges, iSpy, a novel smartphone application, was created to identify foods and determine their carbohydrate content using pictures or speech. This pilot study is to evaluate if using iSpy improves carbohydrate counting accuracy and efficiency. Pilot participants will have carbohydrate counting (accuracy and efficiency) and their overall QoL (with respect to carbohydrate counting) assessed at baseline and after 3-months. The investigators hypothesize that using iSpy will make carbohydrate counting easier (by improving accuracy and efficiency) and enhance QoL for patients and/or their caregivers. If so, iSpy may help lessen the burden of living with T1DM.
Detailed Description
Nutrition is an integral component of management of many chronic diseases and of overall wellness. Helping individuals to understand what they are eating can empower them to better manage their diseases. For example, the growing number of youth living with Type 1 Diabetes Mellitus (T1DM) struggle with carbohydrate counting, an essential and daily aspect of their lives, because of required reliance on memorization and numeracy skills. Effective carbohydrate counting has been demonstrated to improve blood glucose control, while inaccurate carbohydrate counting results in more variable blood glucose. Concerns related to carbohydrate counting accuracy can also limit food choices, provoke anxiety, and decrease quality of life. Since there is no cure for T1DM, enhancing patients' ability to understand and apply carbohydrate counting is an important part in helping them manage their condition most effectively. iSpy is a novel healthcare application that addresses an important clinical need by facilitating carbohydrate counting using pictures or voice recognition. Proprietary algorithms adjust for portion size and identify hidden carbohydrates (such as in ketchup or other condiments) and quantify the amount of carbohydrates in a meal.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 1

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
iSpy
Arm Type
Experimental
Arm Description
In addition to usual care, participants in the intervention group will receive the iSpy intervention.
Arm Title
Control
Arm Type
No Intervention
Arm Description
The control group participants will continue to use their usual method of carbohydrate counting for a 3-month period.
Intervention Type
Device
Intervention Name(s)
iSpy
Intervention Description
iSpy is a novel healthcare application that hopes to address an important clinical need by facilitating carbohydrate counting using pictures or voice recognition. Proprietary algorithms adjust for portion size and identify hidden carbohydrates (such as in ketchup or other condiments) and quantify the amount of carbohydrates in a meal.
Primary Outcome Measure Information:
Title
Carbohydrate (CHO) Counting Accuracy
Description
Assessing CHO counting using 10 food items from all major food groups. For each group, a simple food (e.g. an apple) and complex food (e.g. food with 2+ components but base food from targeted group) is included. A Co-investigator, Registered Dietitian (RD)/Certified Diabetes Educator (CDE), selected 2 sets of 10 food items for the study visits (verified that both sets were similar difficulty). The net CHO value (true value) for each food will be based on the nutrition label, USDA Nutrient Database (Release 28), Canadian Nutrient File, or by RD/CDE. For each food, data will be obtained from all participants: • Estimated net CHO (in grams) And with the above data, the following will be calculated: % of food for which subjects estimated the CHO content within (+/-) 10 grams of true value. Change (%) in the above accuracy measure for counting at baseline versus 3-month follow-up visit in iSpy vs control groups.
Time Frame
3 months
Title
Carbohydrate (CHO) Counting Efficiency (Time to count)
Description
Assessing CHO counting using 10 food items from all major food groups. For each group, a simple food (e.g. an apple) and complex food (e.g. food with 2+ components but base food from targeted group) is included. A Co-investigator, Registered Dietitian (RD)/Certified Diabetes Educator (CDE), selected 2 sets of 10 food items for the study visits (verified that both sets were similar difficulty). The net CHO value (true value) for each food will be based on the nutrition label, USDA Nutrient Database (Release 28), Canadian Nutrient File, or by RD/CDE. For each food, data will be obtained from all participants: • Time required to estimate net CHO (in seconds) In order to calculate the following: • Change in the above time taken for counting at baseline versus 3-month follow-up visit in iSpy vs control groups.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Change in Quality of Life: Self Care Inventory Questionnaire
Description
Quality of Life questionnaires will be analyzed for any change from baseline to 3-month follow-up within both the intervention and control groups. The first questionnaire including: • Self Care Inventory: Scale from 1 (Never do it) to 5 (Always do this as recommended without fail);
Time Frame
3 months
Title
Change in Quality of Life: Diabetes Questionnaire
Description
Quality of Life questionnaires will be analyzed for any change from baseline to 3-month follow-up within both the intervention and control groups. The second questionnaire including: • Diabetes Family Responsibility Questionnaire: Selection of 1 of 3 statements best describing the way each task is handled in the family from 1 (Parent taking responsibility almost all of the time) 2 (Parent and Child sharing responsibility equally) to 3 (Child taking responsibility almost all of the time);
Time Frame
3 months
Title
Change in Quality of Life: Quality of Life for Youth
Description
Quality of Life questionnaires will be analyzed for any change from baseline to 3-month follow-up within both the intervention and control groups. The third questionnaire including: • Quality of Life for Youth: Scale from 0 (Never) to 4 (All the time);
Time Frame
3 months
Title
Change in Quality of Life: Global Quality of Life
Description
Quality of Life questionnaires will be analyzed for any change from baseline to 3-month follow-up within both the intervention and control groups. The last questionnaire including: • Global Quality of Life: Scale from 1 (No Change) to 7 (A great deal better);
Time Frame
3 months
Title
Implementation outcomes: Accrual/Attrition Rates
Description
• Criteria for implementation success will be based on the studies previously conducted by Co-Principal Investigator (JS): Participant accrual (total completed / total enrolled) and attrition rates (total dropouts / total enrolled). Success being defined as accrual rates >70% and attrition rates <15%;
Time Frame
3 months
Title
Implementation outcomes: Engagement
Description
• Levels of engagement will be assessed as follows: Low: defined as less than 1 logged meal every 2 weeks High: defined as greater than 1 logged meal every 2 weeks.
Time Frame
3 months
Title
Implementation outcomes: Acceptability
Description
• Acceptability: 7 item Acceptability e-Scale (AES) regarding level of acceptability from a scale of 1 (low) to 5 (high) of iSpy, with high acceptability being item mean score of 4 on AES. 2 additional qualitative items are included in AES and will be evaluated.
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosed with T1DM for ≥6 months; Completion of initial carbohydrate counting classes; Incorporating carbohydrate counting into treatment regimen; Having access to a smart phone and data plan; Exclusion Criteria: Cognitive impairments or co-morbid physical or psychiatric condition (e.g. blindness, clinical depression, anxiety disorder) that might impact ability to use iSpy; Diagnosis of condition that affects dietary exposure (e.g. celiac disease); Participation in usability study;
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark Palmert
Organizational Affiliation
The Hospital for Sick Children
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Hospital for Sick Children
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 1X8
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33112249
Citation
Alfonsi JE, Choi EEY, Arshad T, Sammott SS, Pais V, Nguyen C, Maguire BR, Stinson JN, Palmert MR. Carbohydrate Counting App Using Image Recognition for Youth With Type 1 Diabetes: Pilot Randomized Control Trial. JMIR Mhealth Uhealth. 2020 Oct 28;8(10):e22074. doi: 10.2196/22074.
Results Reference
derived

Learn more about this trial

A Novel Carbohydrate Counting Smartphone App for Youth With Type 1 Diabetes

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