Real-time Engagement for Learning to Effectively Control Type 2 Diabetes
Who can join
As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.
- Age
- 14 Years to 26 Years
- Sex
- All sexes
- Healthy volunteers
- Not accepted
- Compensation
- Not stated
Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.
What to expect
No one can promise a trial will help you personally — that is what the research is trying to find out.
What participation involves
- Time periods mentioned: 6 months
- Procedures mentioned: Blood draws
Only what the study's summary and detailed description on ClinicalTrials.gov say. Time periods may describe the whole study or a part of it — ask the study team what applies to you.
Show the study's own words
- "Participants will: * Wear a continuous glucose monitoring device for 6 months * Wear a physical activity tracker for 6 months * Use the study smartphone app for 6 months * Complete 3 in-person study visits with fasting blood draws * Report dietary intake intermittently throughout the study"
- Compensation
- Not stated
- Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
- Participants are monitored closely by the research team throughout the study.
- Some participants may receive access to an investigational treatment, which is still being studied.
- Your participation helps researchers learn whether this approach could help future patients.
About this study
In plain language
This study tests whether a smartphone app that links blood sugar and exercise data helps teens and young adults with type 2 diabetes. It will look at blood sugar control over time and changes in physical activity. Participants will use the app and wear blood sugar and activity trackers for 6 months.
The goal of this clinical trial is to learn if a new smartphone app that pairs glucose and exercise data will help adolescents and young adults with type 2 diabetes improve glycemic control. It will also study how changes in glycemic control are maintained over time. The main questions it aims to answer are: * Does using the app help with short-term glycemic control? * Does using the app help with longer-term glycemic control? * Does using the app help increase physical activity? Participants will: * Wear a continuous glucose monitoring device for 6 months * Wear a physical activity tracker for 6 months * Use the study smartphone app for 6 months * Complete 3 in-person study visits with fasting blood draws * Report dietary intake intermittently throughout the study
Compensation is read from the study's own description and may be missing — always confirm with the study team.
Eligibility
Who can join
- Have type 2 diabetes, with negative tests for diabetes autoantibodies (immune proteins linked to other types of diabetes).
- Have no signs that suggest diabetes caused by a change in a single gene.
- Speak English, since the app is in English.
Who can't join
- Are currently pregnant.
- Take hydroxyurea, a medicine that can make the blood sugar sensor less accurate.
- Have problems with thinking or a severe mental health condition that could make it hard to take part in learning diabetes self-care.
- Have an eating disorder now or were diagnosed with one in the past.
Simplified for readability. The official criteria below are what the study team uses.
Official eligibility criteria
Inclusion Criteria: * type 2 diabetes: negative diabetes autoantibodies, no suspicion for monogenic diabetes * English-speaking (app in English) Exclusion Criteria: * Current pregnancy * Hydroxyurea use (CGM sensor inaccuracies) * Cognitive impairment or severe psychiatric condition that could interfere with participation in behavioral intervention for diabetes self-management * Current or previously diagnosed eating disorder
Study sites (1)
PA
- UPMC Children's Hospital of Pittsburgh · Pittsburgh, PA 15224Mary Ellen Vajravelu, MD, MSHP · Study contact · 412-692-6533 · vajravelume@upmc.eduNyesha Rainey, BS · Study contact · 412-692-8418 · raineyns@upmc.eduMore trials in Pittsburgh