Skip to content

Metabolic Wellness and CGM

Assessing the Glycemic Impact of an Online Lifestyle Intervention Using CGM (Continuous Glucose Monitoring). a Pilot Study.

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06790472
Enrollment
100
Registered
2025-01-24
Start date
2024-09-05
Completion date
2025-10-11
Last updated
2025-01-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiometabolic Risk Factors

Keywords

Lifestyle, Online, Metabolic wellness, Cardiometabolic risk, Digital health, Continuous glucose monitoring

Brief summary

The primary objective of this study is to determine the impact of participating in an online lifestyle intervention program on glycemic control as measured by Continuous Glucose Monitoring (CGM), with the primary outcome being the time-in-range (TIR) between 70 and 140 mg/dl comparing before the intervention, at the start of the program (week 1), and after the intervention (week 8).

Detailed description

The Metabolic Wellness Program (MWP) is an established 8-week program that provides participants with digitally delivered health education focusing on metabolic health. The program content is based on nutrition education, promotion of physical activity, stress reduction and the need for quality sleep. The MWP also includes the use of continuous glucose monitoring (CGM), The MWP is aimed at adults with pre-existing type 2 diabetes (T2D), prediabetes and also individuals who wish to retain their metabolic health. (More information about the program is available here: https://www.sutterhealth.org/classes-events/the-metabolic-wellness-program-34466 To evaluate the success (or otherwise) of the MWP, the aim of this pilot study is to assess the impact of participating in the MWP on glycemic control, with the primary outcome being the time-in-range between 70 and 140 mg/dl measured by CGM. Data from this pilot study will provide evidence for a larger future randomized controlled trial (RCTs). The secondary objectives are to: * Examine additional changes in CGM variables comparing before (at baseline)and after the intervention (at week 8 and at 3 months post-intervention) Examine changes in self-reported behavior changes related to food choices, physical activity, sleep quality, and stress levels. * Examine changes in lab values (if available as part of routine clinical care from the previous 12 months and up to 6 months after the program): and * Examine engagement with the program, engagement with CGM, and satisfaction with the program

Interventions

The Metabolic Wellness Program (MWP) is an established 8-week program that provides participants with health education videos and webinars that focus on evidence-based nutrition, fitness, sleep, and stress intervention, including with CGM, allowing participants to monitor their real-time glucose data and to learn which lifestyle choices are best for their glycemic control and personal metabolic health. The program is also intended to help healthy participants maintain their metabolic health and lower their potential risk of developing cardiometabolic disease, as well as at-risk and pre-diabetic participants preventing the progression to T2D and people with established T2D reverse their condition.

DEVICEContinuous Glucose Monitoring

CGM measurements begin at enrollment with training provided digitally Participants will be asked to live life as usual whilst wearing the device with initial 10-14 day readings providing baseline data. Participants will participate in the online lifestyle program, which the investigators refer to as the intervention stage. Participants will also receive questionnaires on behavior change at the beginning of week 5. During the final two weeks of the program (weeks 7-8), the final 10-14 days of CGM will be used as comparison data with baseline information.

Sponsors

William Marsh Rice University
CollaboratorOTHER
Abbott Diabetes Care
CollaboratorINDUSTRY
David Kerr
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Adults who are enrolled in the MWP * Adults ≥ 18 years of age at enrollment. * Willing to wear a CGM device. * Sutter Health employee or employee's dependent enrolled in SutterSelect Employee Medical Benefits

Exclusion criteria

* Pregnancy * Taking insulin * Chronic kidney disease and on dialysis * Any active clinically significant disease or disorder which, in the investigator's opinion, could interfere with participation in the study

Design outcomes

Primary

MeasureTime frameDescription
Glycemic Control (Time-in-Range)Baseline and Weeks 2, 7-8Time-in-range (TIR) between 70 and 140 mg/dl as measured by CGM.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026