Diabetes Data-Assisted Remission Trial (DDART)

Last updated: February 26, 2025
Sponsor: Wake Forest University Health Sciences
Overall Status: Completed

Phase

N/A

Condition

Obesity

Diabetes Mellitus Types I And Ii

Diabetes And Hypertension

Treatment

Continuous glucose monitoring

Diabetes education

Medical weight loss

Clinical Study ID

NCT04663061
IRB00067950
  • Ages > 18
  • All Genders

Study Summary

The study team will study the efficacy of a high intensity medical weight loss intervention paired with a digital platform to create weight loss and induce remission of type 2 diabetes mellitus (T2DM) compared to a diabetes self-management education intervention. The digital platform provides the capability to tailor the treatment plan, provide automated support, and alert providers when a participant may need more support from the clinical team. If shown to be efficacious, this research could be highly impactful, causing us to rethink our approach to care for those with T2DM and shift the paradigm for millions of individuals in the United States. Furthermore, this approach will demonstrate the feasibility of helping people engage in metabolic treatment strategies in a way that is scalable leveraging digital and mobile solutions that extend the patient-provider relationship, shift care from episodic approaches to more of an on-going model that extends into the life of the patient, while also integrated within the healthcare system workflows.

Eligibility Criteria

Inclusion

Inclusion:

  • Individuals with T2DM diagnosed within the past 6 years

  • Body Mass Index (BMI) of 30-39.9 kg/m2.

  • Participants must have an HbA1c between 6.5-11.9%.

  • Participants should be able to participate in all aspects of the recommendedinterventions, including being able to participate in exercise, make recommendeddietary changes, and engage in individual and group counseling.

Exclusion

Exclusion criteria:

  • Poorly controlled depression

  • Recent hospitalization for psychosis or bipolar disorder

  • Poorly controlled blood pressure (>159/99)

  • Prior surgical procedure for weight control or liposuction

  • Unable to make changes to their diet

  • Unable to exercise (walk for at least 6 minutes and perform simple strength andstretch exercise tests)

  • Use of weight loss medications in previous 3 months

  • Recent self-reported weight change (+/- 15lbs)

  • Current use of oral corticosteroids more than 5days/month

  • Cardiovascular disease event within the past 6 months

  • Severe pulmonary disease requiring supplemental oxygen

  • Renal failure (end stage renal disease)

  • History of non-skin cancer in the past 5 years

  • Major liver dysfunction within the last 2 years

  • Recently quit smoking less than 6 months prior

  • Inability to attend visits and adhere to study protocols

  • Pregnancy or currently lactating

Study Design

Total Participants: 65
Treatment Group(s): 3
Primary Treatment: Continuous glucose monitoring
Phase:
Study Start date:
June 09, 2021
Estimated Completion Date:
November 14, 2024

Study Description

This project will determine if a data-assisted, high intensity medical weight loss intervention (HIWL) will lead to significant weight loss and diabetes remission in individuals with a Body Mass Index (BMI) 30-39.9 kg/m2 with T2DM of less than 6 years as compared to a diabetes self-management education intervention (DSME). Complete diabetes remission is considered to be achieved when the patient is not taking any anti-diabetes medication for at least 12 months, and the Glycated Hemoglobin (HbA1c) is < 5.7%. Partial remission is achieved when the patient is not taking any anti-diabetes medication and has an HbA1c of 5.7-6.4% for at least 12 months.Using a randomized controlled study design, we will randomly assign 90 participants to HIWL, HIWL + continuous glucose monitoring (CGM), or DSME. Participants assigned to HIWL will receive a high intensity behavioral weight loss intervention delivered using a digital patient engagement platform. Participants will be prescribed a low calorie dietary plan and a recommended physical activity program designed to produce 15-20% weight loss over 12 months. Those assigned to HIWL + CGM will receive the same intervention as HIWL; in addition we will provide them with CGM to use as part of their remote monitoring on a daily basis. Those assigned to DSME will participate in a comprehensive diabetes education program designed to provide education and skills for optimal diabetes management plus lifestyle modification counseling to produce 5% weight loss over the same timeframe. The primary outcome of weight loss will be assessed at 12 months.

Connect with a study center

  • Wake Forest Univesity Health Sciences

    Winston-Salem, North Carolina 27157
    United States

    Site Not Available

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