High Intensity Body-weight Circuit Training Feasibility and Efficacy for in Middle Aged Persons W… (NCT05571384) | Clinical Trial Compass
CompletedNot Applicable
High Intensity Body-weight Circuit Training Feasibility and Efficacy for in Middle Aged Persons With Type 2 Diabetes
United States22 participantsStarted 2022-07-26
Plain-language summary
This research study proposes to quantify the efficacy of the novel high intensity body-weight circuit (HIBC) training intervention on metabolic profile, body composition, and health related fitness exercise in middle aged persons with type-2 diabetes (T2DM). This research project is extremely relevant to public health, in that prevalence of T2DM continues to rise on a national and global scale, placing a heavy economic cost on both the healthcare industry and the individual patient in an age-dependent fashion. Results of this study may provide an effective and appealing alternative exercise intervention for cardiometabolic disease management in adults with T2DM, and have significant clinical and public health applications.
Who can participate
Age range
40 Years – 65 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:
* Recent diagnosed of type 2 diabetes (T2DM) (within a year) \* HbA1c of 6% or higher
* Non-insulin dependent
* No medicinal treatment
* Not currently undergoing a physical activity program in the last six months
* Received written medical clearance from overseeing physician
Exclusion Criteria:
* Those who have undergone any revascularization procedure
* Diagnosed with or symptomatic of any renal, pulmonary, or cardiovascular disease (CVD)
* Diagnosed cognitive dysfunction
* Current smoker
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.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
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.
What they're measuring
1
HbA1c change within participant
Timeframe: Pre and post 16-week intervention
2
Oral Glucose Tolerance Test change within participant
Timeframe: Pre and post 16-week intervention
3
Body Composition change within participant
Timeframe: Pre and post 16-week intervention
4
Estimated VO2max (oxygen consumption), aerobic exercise capacity change within participant