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Precision Nutrition Counseling in Type 2 Diabetes Patients

Development of Precision Nutrition Counseling in Type 2 Diabetes Patients: Using Continuous Glucose Monitoring System

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04266171
Enrollment
50
Registered
2020-02-12
Start date
2020-01-16
Completion date
2021-12-31
Last updated
2020-02-12

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

Conditions

Type 2 Diabetes

Keywords

continuous glucose monitor, diet education, Precision nutrition

Brief summary

The aim of this study is to evaluate the effect of precision nutrition education using continuous glucose monitoring system (CGMS) in longterm glycemic control in patients with type 2 diabetes mellitus. Glucose levels in subjects who received diet education using CGMS will be compared to those in subjects who received conventional diet education.

Detailed description

Fifty subjects with type 2 diabetes will be recruited. Every subject will be randomized in two groups, which are CGMS education group and conventional education group. The study will be conducted for 12 weeks for each participants. Intervention group will receive diet education based on CGMS data, using post prandial glucose response, calculated by incremental area under curve of glucose level. Control group will receive conventional diabetes diet education without CGMS data. Primary outcome is change of HbA1c from baseline for 12 weeks, and secondary outcomes are changes of fasting blood glucose level, body weight, waist circumference, blood lipid level, homeostatic model assessment of insulin resistance (HOMA-IR) , c-peptide, microbiome, 7-point self monitoring of blood glucose (SMBG), and compliance/satisfaction questionnaire from baseline for 12 weeks.

Interventions

BEHAVIORALDiet education based on CGMS data

Intervention group will receive diet education based on CGMS data, using post prandial glucose response, calculated by incremental area under curve of glucose level. Control group will receive conventional diabetes diet education without CGMS data.

BEHAVIORALConventional diet education

Control group will receive conventional diabetes diet education without CGMS data.

Sponsors

ChunLab
CollaboratorUNKNOWN
Seoul National University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 79 Years
Healthy volunteers
No

Inclusion criteria

* Type 2 diabetes patients (Fasting blood glucose ≥ 126 mg/dl or HbA1c ≥ 6.5% or Subjects who were previously diagnosed with type 2 diabetes and who have been treated with lifestyle modification only, oral anti-diabetic drugs or basal insulin) * HbA1c 6.5%\ 10% * Body weight change less than 5% in 3 month * Subjects who agreed to the study protocol

Exclusion criteria

* Type 1 diabetes patients * Subjects using insulin other than basal insulin * Subjects who have newly started or have changed anti diabetic drugs within 3 months * Subjects who have been received diabetes diet education within 6 months * Females who are pregnant or doing breast feeding * Subjects with alcohol addiction or drug abuse * Subjects who are using drugs that can influence blood glucose levels (e.g. steroid) * Subjects who are currently using acetaminophen or who should use acetaminophen during CGMS attach period * Subjects who have skin problems on CGMS sensor insertion site (e.g. burn, excessive body hair, inflammation, rash, tattoo) * Subjects who have newly started, changed, or stoped probiotics or prebiotics within 2 weeks * Subjects who have used antibiotics (oral or intravenous) within 2 weeks * In addition, if it falls under the

Design outcomes

Primary

MeasureTime frame
Change in HbA1c from baseline0 week, 12 weeks

Secondary

MeasureTime frameDescription
Change in body weight from baseline0 week, 12 weeks
Change in waist circumference from baseline0 week, 12 weeks
Change in blood Triglyceride level from baseline0 week, 12 weeks
Change in blood High-density lipoprotein level from baseline0 week, 12 weeks
Change in blood Low-density lipoprotein level from baseline0 week, 12 weeks
Change in fasting blood glucose level from baseline0 week, 12 weeks
Change in c-peptide from baseline0 week, 12 weeks
Change in microbiome profile from baseline0 week, 12 weeksChange in the diversity index of the gut microbiota, change in the compositions of the gut microbiota
Change in 7-point SMBG from baseline0 week, 12 weeks
Compliance/Satisfaction Questionnaire0 week, 12 weeksChange in dietary habits, self-efficacy of diet management , and satisfaction with the education
Change in HOMA-IR from baseline0 week, 12 weeks

Countries

South Korea

Outcome results

None listed

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