ClinicalTrials.gg
CompletedNCT06769906Updated Jan 2, 2026

Effectiveness of Individualized Automatic Coaching Message for Glycemic Management and Depressive Symptom

An interventional study of Individualized automatic coaching message for glycemic management and depressive symptom in Diabetes Mellitus Type 2, Continuous Glucose Measurement and Depressive Symptom, sponsored by Samsung Medical Center. Completed at 1 site in South Korea. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-01-02.

Sponsored by Samsung Medical Center · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
46
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
01

Study summary

This is a 12-week, single-center, randomized, prospective, confirmatory study of effectiveness of the individualized automatic coaching messages for glycemic management based on continuous glucose monitoring and depressive symptom in insulin-treated patients with type 2 diabetes.

Read the detailed description

This study will enroll patients with type 2 diabetes who are insulin-treated outpatient care at the Department of Endocrinology and Metabolism, Samsung Medical Center. For 12 weeks, both intervention and control groups will apply continuous glucose monitoring system. The intervention group will receive weekly personalized coaching messages for glycemic management based on data from continuous glucose monitoring and bi-weekly personalized coaching messages for depressive symptoms based on depression questionnaires. The control group will not receive the coaching messages. The aim of this study is to evaluate whether the efficacy of individualized automatic target coaching messages based on continuous glucose monitoring metrics and depressive symptom assessments is superior to those who do not receive the messages in insulin-treated patients with type 2 diabetes.

02

Conditions studied

  • Diabetes Mellitus Type 2
  • Continuous Glucose Measurement
  • Depressive Symptom

Keywords

  • Behavioral Symptom
  • Glucose Metabolism Disorders
  • Endocrine System Diseases
  • Diabetes Mellitus, Type 2
  • Continuous glucose monitoring
  • Depression
  • Diabetes Mellitus
  • Metabolic Diseases
03

In context

Diabetes Mellitus, Type 2

10,371 studies on the registry are indexed under Diabetes Mellitus, Type 2; 1,406 are open to participants now.

This study's enrollment of 46 is below the median of 80 across 8,350 interventional studies indexed under Diabetes Mellitus, Type 2.

Browse Diabetes Mellitus, Type 2 studies →

Lead sponsor

Samsung Medical Center is the lead sponsor of 1,011 studies on the registry; 152 are open to participants now.

Of its 7 completed or terminated interventional studies of FDA-regulated products, 1 (14%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients for whom the use of a continuous glucose monitor has been determined based on the medical judgment of the attending physician.
  • Insulin-treated type 2 diabetes patients, age 18-80 years old.
  • Patients who have not changed their diabetes medication in the past 2 months.
  • Patients with a level between 6.5% and 12.0% within the last 3 months.
  • Patients currently receiving insulin injection therapy, including basal insulin.
  • Patients who have access to KakaoTalk via smartphone and are able to communicate with it.
  • Voluntarily agreed to participate in this clinical study.

Exclusion criteria

Exclusion Criteria:

  • and users. But it can be included if patients continuously maintain same drug dose at least three months.
  • Patients who are currently taking weight control medications.
  • Breastfeeding or pregnant patients
  • Patients who do not voluntarily consent to the study
  • Anyone deemed unsuitable by the investigator to participate in the study
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

HbA1c

A blood test of average blood sugar over the past two to three months, given as a percentage or in mmol/mol. 6.5% (48 mmol/mol) or more is the usual threshold for diabetes, normally confirmed by a second test.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
46 participants (actual)

Study arms

  • Experimental
    Individualized automatic coaching message for glycemic management and depressive symptoms

    The study will enroll insulin-treated patients with type 2 diabetes who are already receiving standard care and diabetes management through outpatient visits. For 12 weeks, the intervention group and control will apply continuous glucose monitoring. The intervention group will receive weekly personalized coaching messages for glycemic management based on data from continuous glucose monitoring and bi-weekly personalized coaching messages for depressive symptoms based on depression questionnaires for 12 weeks.

    Other: Individualized automatic coaching message for glycemic management and depressive symptom

  • No intervention
    Control

    The control group will continue their existing treatment and wear a continuous glucose monitoring device, responding to both surveys by accessing the survey link sent to their cell phone. This will allow for the assessment of baseline satisfaction (DTSQ) and depressive symptoms (PHQ-9).

Interventions

  • OtherIndividualized automatic coaching message for glycemic management and depressive symptom

    For 12 weeks, the intervention group will apply continuous glucose monitoring system and receive weekly personalized coaching messages for glycemic management based on data from continuous glucose monitoring and bi-weekly personalized coaching messages for depression symptoms based on depression questionnaires.

06

What researchers measure

Primary outcomes

  1. Time In Range

    Derived from continuous glucose monitoring (CGM)

    Time frame: Week 12

Secondary outcomes

  1. Diabetes treatment satisfaction

    Diabetes Treatment Satisfaction Questionnaire (DTSQ); Minimum and Maximum Values: The DTSQ consists of eight items, with six items measuring satisfaction scored on a 0-6 scale (where 0 is very dissatisfied and 6 is very satisfied). The scores for these six items are summed, giving a total score range from 0 to 36. Higher Scores: Higher scores on the DTSQ indicate better satisfaction with diabetes treatment. A higher total score suggests greater satisfaction, while a lower score indicates dissatisfaction.

    Time frame: Week 12

  2. Depressive symptoms

    Patient Health Questionnaire-9 (PHQ-9); Minimum and Maximum Values: The PHQ-9 consists of nine items, each scored from 0 (not at all) to 3 (nearly every day). The scores for each item are summed to give a total score, resulting in a range from 0 to 27. Higher Scores: Higher scores on the PHQ-9 indicate worse outcomes, meaning greater severity of depressive symptoms. Lower scores suggest fewer symptoms of depression or none at all. Interpretation of Scores: 0-4: Minimal or no depression; 5-9: Mild depression; 10-19: Moderate depression; 20-27: Severe depression

    Time frame: Week 12

  3. Time In Tight Range

    Derived from CGM

    Time frame: Week 12

  4. Level of glycated Hemoglobin

    Derived from blood measurement

    Time frame: Week 12

  5. Time Above Range

    Derived from CGM

    Time frame: Week 12

  6. Time Below Range

    Derived from CGM

    Time frame: Week 12

  7. Coefficient of Variation

    Derived from CGM

    Time frame: Week 12

  8. Glycemic Management Indicator

    Derived from CGM

    Time frame: Week 12

Other outcomes

  1. Level of Albuminuria

    Urine creatinine-to-albumin ratio

    Time frame: Week 12

  2. Level of Glycated albumin

    Glycated albumin

    Time frame: Week 12

  3. Level of triglycerides

    Level of triglycerides from blood measurement

    Time frame: Week 12

  4. Level of total cholesterol

    Level of total cholesterol from blood measurement

    Time frame: Week 12

  5. Level of HDL (high density lipoprotein) cholesterol

    Level of HDL cholesterol from blood measurement

    Time frame: Week 12

  6. Level of LDL (low density lipoprotein) cholesterol

    Level of LDL cholesterol from blood measurement

    Time frame: Week 12

07

Study locations

1 site
  • Samsung Medical Center
    Seoul, South Korea
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 2, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06769906
Responsible party
Gyuri Kim (Principal Investigator, Samsung Medical Center) — Principal investigator
First posted
Jan 10, 2025
Start date
Jan 9, 2025
Primary completion
Jul 2, 2025
Completion
Jul 2, 2025
Last update
Jan 2, 2026

Study contacts

GYURI KIM
principal investigator · Samsung Medical Center

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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