Preventing Diabetes With Digital Health and Coaching for Translation and Scalability (PREDICTS)
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- PreDiabetes
- Sponsor
- Omada Health, Inc.
- Enrollment
- 598
- Locations
- 1
- Primary Endpoint
- HbA1c reduction
- Status
- Completed
- Last Updated
- 5 years ago
Overview
Brief Summary
The goal of this randomized controlled trial is to determine the efficacy of a digital diabetes prevention program for improving weight, glucose control, and secondary risk factors among people with prediabetes compared to an enhanced standard care plus wait-list control. Exploratory assessments of implementation facilitators and barriers will also be completed to determine strategies for integrating external diabetes-prevention interventions within healthcare settings.
Detailed Description
Prediabetes is an increasingly prevalent condition, characterized by glucose levels that are above normal but below the threshold for diabetes. Previous studies have demonstrated that intensive lifestyle interventions targeting changes in diet, physical activity, sleep, and stress can reduce the risk of progressing from prediabetes to Type 2 diabetes. The Diabetes Prevention Recognition Program (DPRP) currently recognizes both in-person and online programs that meet requirements to deliver approved curriculum, provide health coaching and group support, and equip participants with behavioral skills and self-monitoring tools to support behavior change. While non-randomized trial data demonstrate that an online digital program was successful for producing meaningful weight loss and improved glucose control, the goal of this randomized, controlled trial is to definitively evaluate the efficacy of the program for improving weight, glucose control and secondary risk factors compared to current standard care for prediabetes. In addition, few trials have examined the implementation factors that could speed the uptake of efficacious diabetes prevention interventions for delivery in regular clinical practice. Qualitative information on key organizational stakeholders (e.g., physicians, office managers) will be gathered to provide information on perceptions of the online program characteristics, outcomes, and resources concurrently with strategies to promote adoption and implementation in health care settings.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Receives care at University of Nebraska Medical Center or Nebraska Medicine
- •Age 19 years or older
- •HbA1c 5.7%-6.4%
- •Overweight (BMI 25+ or 22+ if Asian)
- •Planning to reside in recruitment area for next 12 months
- •Able to engage in moderate aerobic physical activity
- •Medically stable
- •Able to provide informed consent
- •Willing to accept random assignment to treatment
Exclusion Criteria
- •Not meeting all inclusion criteria
- •Diagnosed with Type I or II diabetes
- •Diagnosed with congestive heart failure, coronary artery disease, chronic obstructive pulmonary disease, pulmonary hypertension
- •Diagnosed with dementia or probable Alzheimer's disease
- •Taking oral hypoglycemic agents
- •Participating in a concurrent weight management program or interventional research protocol
- •Unable to engage in physical activity
- •On a prescribed medical diet
- •Had bariatric surgery within the past 3 years or planning surgery within the next 12 months
- •Anti-obesity or diabetes therapy within the preceding 4 months
Outcomes
Primary Outcomes
HbA1c reduction
Time Frame: Baseline and 12 months
Change in percent HbA1c
Secondary Outcomes
- Weight loss(Baseline, 4 months, and 12 months)
- Decreased cardiovascular risk(Baseline, 4 months, and 12 months)