grant

Personalized Nutrition Using Continuous Glucose Monitoring to Improve Outcomes in Type 2 Diabetes Mellitus

Organization UNIVERSITY OF MINNESOTALocation MINNEAPOLIS, UNITED STATESPosted 16 Dec 2024Deadline 30 Nov 2027
NIHUS FederalResearch GrantFY202521+ years oldAdultAdult HumanAdult-Onset Diabetes MellitusAgonistBMIBMI percentileBMI z-scoreBlindedBlood GlucoseBlood SugarBody mass indexClient satisfactionClinical TrialsContinuous Glucose MonitorCounselingD-GlucoseDataDextroseDiabetes MellitusDietDietary InterventionDietitianDiseaseDisorderDoseDrugsEatingEducationEducational aspectsEnrollmentExclusionFailureFastingFeedbackFoodFood IntakeFood PreferencesFutureGLP-1 receptorGLP-I receptorGlucoseGlycohemoglobin AGlycosylated hemoglobin AHb A1Hb A1a+bHb A1cHbA1HbA1cHemoglobin A(1)Humulin RHypoglycemiaIndividualInstructionInsulinInterventionKetosis-Resistant Diabetes MellitusLiteratureMaturity-Onset Diabetes MellitusMeasuresMedical Nutrition TherapyMedicationMissionMonitorMulti-center trialMulticenter TrialsNIDDKNIDDMNational Institute of Diabetes and Digestive and Kidney DiseasesNon-Insulin Dependent DiabetesNon-Insulin-Dependent Diabetes MellitusNoninsulin Dependent DiabetesNoninsulin Dependent Diabetes MellitusNovolin RNutritionNutrition InterventionsNutrition TherapyNutritional InterventionsParticipantPatient SatisfactionPatientsPatternPersonsPharmaceutical PreparationsQuestionnairesQuetelet indexRandomizedRandomized, Controlled TrialsRecommendationRegular InsulinRoleSelf EfficacySlow-Onset Diabetes MellitusStable Diabetes MellitusSulfonylurea CompoundsSurvey InstrumentSurveysSystemT2 DMT2DT2DMTestingTimeType 2 Diabetes MellitusType 2 diabetesType II Diabetes MellitusType II diabetesadult onset diabetesadulthoodcompare to controlcomparison controlcontinuous blood glucose monitorcontinuous blood sugar monitorcontinuous glucose measurementcontinuous sugar monitorcost effectivedesigndesigningdiabetesdiabetes educationdiabetes managementdiabetes mellitus managementdiabetes self-carediabetes self-managementdiabetic managementdiet adherencediet choicediet educationdiet interventiondiet preferencedietarydietary adherencedietary choicedietary guidelinesdietary preferencesdietsdosagedrug/agenteffectiveness testingeffectiveness trialenrollfastedfasting glucosefastsfood choiceglucagon-like peptide-1 receptorglycemic controlgroup interventionhemoglobin A1chypoglycemichypoglycemic episodesimprovedimproved outcomeindividualized nutritionketosis resistant diabeteslife style interventionlifestyle interventionmaturity onset diabetesnew approachesnovel approachesnovel strategiesnovel strategynutrition educationpersonalization of treatmentpersonalized medicinepersonalized nutritionpersonalized therapypersonalized treatmentrandomisationrandomizationrandomized control trialrandomly assignedresponsesatisfactionsexsocial rolesulfonylureatooltype 2 DMtype II DMtype two diabetesvirtual health visitvirtual visit
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Full Description

ABSTRACT
Medical nutrition therapy can be an accessible, cost effective and powerful tool for treatment of type 2 diabetes

mellitus (T2DM), but this potential has not been realized for all patients. A common shortcoming of dietary

strategies is failure to provide personalization, despite increasing evidence showing interpersonal variability in

blood glucose response to meals. This disconnect diminishes the ability of dietary interventions to optimize

glycemic control and may lessen patient satisfaction, diabetes self-efficacy, and long-term diet adherence.

Continuous glucose monitoring (CGM) systems give real-time glucose data that could provide a solution; data

from the literature support the efficacy of CGM use during lifestyle interventions for diabetes and suggest use

of CGM can improve hemoglobin A1c (HbA1c), reduce glycemic variability, and increase diabetes self-efficacy.

The overall objective of this proposal is to compare medical nutrition therapy personalized by CGM feedback to

three control interventions in participants with T2DM. A 12-week randomized controlled trial will enroll 72 adult

participants with T2DM and baseline hemoglobin A1c of 6.8-8.5% in a factorial design (18 per intervention

group): 1) Unblinded CGM/Nutrition Therapy, 2) Blinded CGM/Nutrition Therapy, 3) Unblinded CGM/No

Nutrition Therapy, or 4) Blinded CGM/No Nutrition Therapy. The central hypothesis is that CGM-informed

personalized nutrition therapy is superior to improve glycemic control in T2DM compared to medical nutrition

therapy alone or unblinded CGM use alone. A secondary hypothesis is that CGM-informed personalized

nutrition will improve patient satisfaction and diabetes self-efficacy. Specific aims are 1) to determine if medical

nutrition therapy with active adjustment based on CGM data is superior to control interventions for

improvement of glycemic control of T2DM, and 2) to test if this new approach is acceptable to participants with

T2DM, and if it improves treatment satisfaction, diet satisfaction, and diabetes self-efficacy scores measured

by previously validated questionnaires.

It is anticipated that this project will demonstrate feasibility and produce preliminary data for a future fully

powered effectiveness trial testing our CGM-informed personalized nutrition approach. Potential benefits of this

approach include improved glycemic control and increased diabetes self-efficacy for patients with T2DM. An

additional advantage is that this strategy could be easily adapted to individual and cultural food preferences,

making it broadly acceptable and readily adaptable to a wide range of patients with T2DM. This project is a

critical next step to plan for a longer, larger multicenter trial to definitively test the effectiveness of this new and

exciting approach.

Grant Number: 1R01DK139020-01A1
NIH Institute/Center: NIH

Principal Investigator: Anne Bantle

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