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Impact of mentor functions and smartphone apps on diet therapy and QOL

The impact of mentor functions in a new self-monitoring blood glucose device and smartphone applications for diet therapy and treatment satisfaction - MAP-DS study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1042250018
Enrollment
140
Registered
2025-04-30
Start date
2025-04-30
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Diabetes Mellitus Self-Monitoring of Blood Glucose

Interventions

Patients with diabetes who received insulin therapy or injectable GLP-1 receptor agonist and are on SMBG within insurance coverage will be included. This is a single-center, single-arm pilot study wit

Sponsors

Kumashiro Naoki
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients with diabetes age 18 years or older 2) Patients receiving insulin therapy or injectable GLP-1 receptor agonist medication and have been on SMBG for at least 12 weeks with insurance coverage. 3) Patients using SMBG devices that do not have a mentor function and are not able to utilize the application in a mobile tool, or using SMBG devices with a mentor function and are not using the application in a mobile tool. 4) Own a personal smart phone. 5) Smartphone application is available. 6) HbA1c less than 10.0% at the time of eligibility determination 7) Patients who were obtained written consent.

Exclusion criteria

Exclusion criteria: 1) Diabetic ketoacidosis 2) History of severe hypoglycemia with coma or loss of consciousness 3) Severe infection or serious trauma 4) History of hospitalization within 12 weeks prior to consent 5) Proliferative diabetic retinopathy or maculopathy requiring immediate treatment 6) Patients with malignant tumors and collagen diseases in poor condition despite treatment 7) Women in pregnant or possible pregnant 8) Diagnosed or suspected dementia (the Dementia Assessment Sheet for Community-based Integrated Care System-8 items (DASC-8) score of 11 or more) 9) Patients who were deemed inappropriate for the participation by the principal investigater or investigators

Design outcomes

Primary

MeasureTime frame
Change in total score of DTR-QOL

Secondary

MeasureTime frame
Change in the following No.1-5 from 0 to 24 weeks 1. HbA1c 2. Percentage of blood glucose 180 mg/dL 3. Nutrient and energy intake evaluated by the Brief-type self-administered Diet History Questionnaire (BDHQ) 4. Number of SMBG tests 5.Bodyweight Factors which affect the change in total score of DTR-QOL

Contacts

Public ContactMaki Ikoma

Department of Diabetology and Endocrinology, Kanazawa Medical University

endocrin@kanazawa-med.ac.jp+81-76-286-2211

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026