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OpenTrials
Completed

NCT Number: NCT02556398

Use of Mobile-based Technologies to Improve Diabetes Self-management and Postprandial Glucose Control

The project involve evaluation of a web-based nutrition education program and pilot-testing of a new smartphone app for real-time data logging to identify factors causing glycemic variability.

Completed

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Key information

Age range

25 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Joslin Diabetes Center

Boston, Massachusetts, 02215, United States

About this study

The intervention will be three (3) months in duration and will entail use of a smart phone app for real-time data logging to identify factors causing glycemic variability, as well as use of a web-based nutrition education program. The investigators postulate that the interactive nutrition education curriculum - which will provide feedback to patients about the inter-relationship between their food intake and postprandial glucose profiles, as well as practical guidance for improvements - will lead to a change in food choices and improved post-prandial glucose control.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Individuals that satisfy all of the following conditions will be considered for participation:

  • Must be between the ages of 25 - 75 years of age (inclusive)
  • Type 1 diabetes diagnosis at least 1 year, treated with multiple daily injections or insulin pump.
  • A1c 7.5-9.0%

Exclusion criteria

  • Current or past use of real-time CGM for more than 2 months.
  • Pregnancy (self-reported) or planning conception in next 6 months.
  • History of disordered eating, actively trying to lose weight or planning to do so, BMI > 30 kg/m2 (to limit participation by individuals who are actively trying to lose weight),
  • Medical conditions or medications that would affect gastric emptying such as gastroparesis, bariatric surgery, medications such as pramlinitide, liraglutide or exenatide.

Treatment and study plan

Sugar Sleuth

Behavioral

Educational module and use of smart phone app ("Sugar Sleuth")

Primary outcomes

  1. area under the curve (AUC) above target (> 180 mg/dL)

    Time frame: 3 months

    Amount of time spent above >180 mg/dL on CGM Freestyle Libre readings

Sponsors and collaborators

Lead sponsor

Joslin Diabetes Center

Other

Registry information

Important dates

Study start
2015
Primary completion
2017
Study completion
2021
First posted
Sep 22, 2015
Registry last updated
Sep 5, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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