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Continuous Glucose Monitoring to Aid Weight Loss in Prediabetes

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Stanford University

Status

Terminated

Conditions

Weight Loss
PreDiabetes

Treatments

Other: Dietitian
Device: CGM

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT03844646
P30DK116074 (U.S. NIH Grant/Contract)
49402

Details and patient eligibility

About

The primary objective of this study is to determine whether intermittent use of continuous glucose monitor will facilitate weight loss in individuals who are overweight/obese with prediabetes.

Full description

Continuous glucose monitoring (CGM) has revolutionized the treatment of patients on intensive insulin therapy and its utility can also be harnessed to help individuals with prediabetes make healthful lifestyle changes. Successful weight loss requires adherence to lower calories, regular exercise, and self-monitoring. This proposal will test the hypothesis that intermittent CGM will facilitate all of these components for successful weight loss by functioning as a continuous self-monitor and guiding healthful food choices and physical activity.

Enrollment

12 patients

Sex

All

Ages

18 to 99 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Overweight/obese (BMI 25-40 kg/m2)
  • Prediabetes (fasting glucose 100-125 mg/dL and/or HbA1c 5.7-6.4%)

Exclusion criteria

  • On glucose-lowering medications (e.g., metformin)
  • On weight-loss medications

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

12 participants in 2 patient groups

CGM plus dietitian
Experimental group
Description:
Intermittent use of a continuous glucose monitor (CGM) plus dietitian support
Treatment:
Other: Dietitian
Device: CGM
Dietitian only
Other group
Description:
Dietitian support only
Treatment:
Other: Dietitian

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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