Dept. of Psychiatry and Neurobehavioral Sciences, University of Virginia
Charlottesville, Virginia, 22908, United States
NCT Number: NCT03196895
Conventional lifestyle modification in the management of type 2 diabetes focuses on weight loss, through caloric restriction and exercise, to reduce insulin resistance. This approach is limited because some people either do not need to lose weight, do not want to lose weight, cannot lose weight, or cannot maintain weight loss over a lifetime. This study proposes to evaluate the effectiveness of a lifestyle modification that focuses on reducing post-meal blood glucose (BG) elevations instead of weight loss. It works by teaching participants to: 1) choose low glycemic load foods that do not significantly increase their blood glucose, and 2) increase their routine physical activity after meals when it can offset post-meal blood glucose elevations. The study will also evaluate the role feedback about blood glucose fluctuations can play in improving the effectiveness of this program.
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Notify Me21 year–80 year
All sexes
Interventional
Not applicable
Charlottesville, Virginia, 22908, United States
BACKGROUND: Type 2 diabetes (T2D) is a growing epidemic in the U.S. with devastating complications that result in major health and personal costs. To address this, the American Diabetes Association recommends a lifestyle program that focuses on weight loss through caloric restriction and exercise as an initial or an adjunct treatment to pharmacological interventions. However, its general applicability is limited because some individuals with T2D do not need to lose weight, do not want to lose weight, cannot lose weight, or cannot maintain weight loss over a lifetime. Recent research indicates that a major contributor to poor metabolic control is postprandial glucose (PPG) elevation. The researchers have developed a treatment option that focuses on reducing PPG without requiring weight loss. This lifestyle program is comprehensive, integrated, and efficient. Over 5 sessions, this program empowers individuals to use Glycemic load of food, Exercise, and Monitoring glucose (GEM) in a systematic manner. GEM's 1.03% HbA1c reduction compared favorably to both conventional weight loss (0.64% reduction with 42 sessions of Look AHEAD) and continual use of a first line medication (0.9% reduction with Metformin). When enhancing the quantity and quality of glucose feedback with Continuous Glucose Monitoring (CGM), GEM reduced HbA1c by 1.30%.
AIMS: This project will determine how GEM compares to conventional weight reduction at short- and long-term follow-up in a large, representative sample of adults with type 2 diabetes. At the same time, the researchers will test a conceptual model based on a review of the literature postulating that the effects of GEM are modulated by the quality and quantity of glucose feedback. This has important implications for long-term maintenance; since the model proposes a cascade in which increasing either the quantity or quality of glucose feedback improves immediate behavior change through positive and negative glucose consequences. These contingencies may lead to improved PPG and insulin sensitivity, and in turn, improved metabolic control. This cascade may produce ancillary benefits that could help maintain long-term success, e.g. greater empowerment and fewer depressive symptoms.
APPROACH: 200 participants with poorly controlled T2D will be randomized to 1 of 4 groups that manipulate both the focus on postprandial glucose and the quality and quantity of glucose feedback. Short- and long-term benefits will be assessed using medical, behavioral and psychological measures obtained at baseline, 3 months post-intervention and 12 months post-intervention.
IMPACT: If GEM is shown to be effective and enduring, it will provide an alternative to the conventional weight-loss focused lifestyle modification. GEM has the potential to improve metabolic control, increase self-reliance, and slow disease progression. Because GEM is manual-based, it will be easy to deploy and will give it the potential to impact a large proportion of the adults with T2D.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
6 one-hour sessions of conventional weight reduction training
Four 90-minute sessions of glycemic load and exercise training
Blood glucose feedback from structured self-monitoring of blood glucose
blood glucose feedback from continuous glucose monitoring
Time frame: baseline, 3 months, and 12 months post-intervention
change in HbA1c from baseline measure
Time frame: baseline, 3 months, and 12 months post-intervention
change in medication type or dose from baseline measures
Time frame: baseline, 3 months, and 12 months post-intervention
ASA24 survey across 3 separate days in each time frame
Time frame: baseline, 3 months, and 12 months post-intervention
At assessment visits, subjects will choose between energy bars that do or dont support the intervention principles.
Time frame: baseline, 3 months, and 12 months post-intervention
daily activity will be recorded
Time frame: baseline, 3 months, and 12 months post-intervention
The Food Questionnaire
Time frame: baseline, 3 months, and 12 months post-intervention
WHOQO-BREF questionnaire
Time frame: baseline, 3 months, and 12 months post-intervention
Patient Health Questionnaire (PHQ-9)
Time frame: baseline, 3 months, and 12 months post-intervention
Numeracy Scale - measures how good one is with numbers
Time frame: baseline, 3 months, and 12 months post-intervention
Diabetes Knowledge Scale
Time frame: baseline, 3 months, and 12 months post-intervention
Diabetes Empowerment Scale
Time frame: baseline, 3 months, and 12 months post-intervention
Diabetes Distress Scale (Emotional Distress & Regimen Distress subscales)
Time frame: baseline, 3 months, and 12 months post-intervention
The Glucose Monitoring Satisfaction Survey (GMSS)
University of Virginia
Other
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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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