BridgeMD
New treatment option for PreDiabetes
Official title The YMCA Healthy Lifestyle Program for Prediabetes
ClinicalTrials.gov ID: NCT06841796
What this study is testing
- What it's testing
- The goal of this 26 week randomized controlled clinical trial is to learn if using a real time continuous glucose monitor (CGM) in a healthy lifestyle program for adults with prediabetes at the YMCA can improve glucose levels, dietary habits and physical activity The main questions it aims to answer is Does use of a CGM improve the percent of time spent with glucose values between 70-140 mg/dl Does use of a CGM improve nutritional habits as measured by Picture Your Plate (PYP) score Does use of a CGM improve physical activity as measured by International Physical Activity Questionnaire (IPAQ) score Researchers will compare individuals using real time CGM to those not using CGM Participants will be asked to: attend weekly health coach sessions for 12 weeks followed by 3 monthly sessions. attend a YMCA class of their choice fill out questionnaires at baseline, 12 and 24 weeks have an A1c blood test at baseline, 12 and 24 weeks.
- You might receive a placebo (an inactive treatment) instead of the study drug, decided by chance. You may not know which one you got.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- ● Adults 18 years or older AND
- A diagnosis of prediabetes as defined by:
- Fasting glucose 100-125 mg/dl OR
- A1c 5.7-6.4%
You likely can't join if
- Pregnancy
- Previous CGM use
- Lack of smart phone/smart device
- Use of steroids
- Active cancer treatment
- Active chronic infection requiring long term use of antibiotics
See the full eligibility criteria
- ● Adults 18 years or older AND
- A diagnosis of prediabetes as defined by:
- Fasting glucose 100-125 mg/dl OR
- A1c 5.7-6.4%
- Pregnancy
- Previous CGM use
- Lack of smart phone/smart device
- Use of steroids
- Active cancer treatment
- Active chronic infection requiring long term use of antibiotics
- Terminal illness
- Dementia, mental impairment
- Non English speaking
The study team makes the final eligibility decision.
Where it's taking place
- Port Huron, Michigan, United States
Compensation & support
A stipend or compensation may be offered.
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Port Huron, Michigan, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.