Scale-Up Evaluation Trial of the Diabetes Prevention Program to Improve Obesity and Cardiometabol… (NCT07648901) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Scale-Up Evaluation Trial of the Diabetes Prevention Program to Improve Obesity and Cardiometabolic Health After Traumatic Brain Injury
United States70 participantsStarted 2026-08-15
Plain-language summary
The Investigators have proposed targeted efforts to address the feasibility, effectiveness, fidelity, and evaluation of the GLB-TBI Evidence Based Intervention (EBI) in a real world setting at a CDC-recognized site
Who can participate
Age range
18 Years – 80 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
≥6 months post-TBI
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1This trial is adapting the Diabetes Prevention Program specifically for people with traumatic brain injury — given my TBI history and current health, does my doctor think this kind of structured lifestyle intervention would be appropriate and safe for me to consider once it opens?
2The trial is not yet recruiting, so it could be a while before I could even join — should I be doing anything now, like standard diabetes prevention or weight management programs, while I wait to see if this study becomes available?
3Since the trial is in a 'not applicable' phase focused on scaling up an existing program rather than testing a new drug, how confident can my doctor be that the approach is already reasonably safe, and what risks, if any, should I still be aware of given that my brain injury could affect how I respond to a lifestyle intervention?
4The main thing being measured is body weight, but I'm also concerned about my overall cardiometabolic health after my TBI — should I ask my doctor whether this trial will also track things like blood sugar or blood pressure, and whether those outcomes matter for my specific situation?
5Because this is a scale-up evaluation rather than a first-in-humans study, what would my doctor recommend I ask the research team about how they plan to adapt the program to account for TBI-related challenges like cognitive fatigue, memory difficulties, or physical limitations??
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.