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A study to evaluate the efficacy of the Teaching Kitchen program in Japanese patients with diabetes

A study to evaluate the efficacy of the Teaching Kitchen program in Japanese patients with diabetes - A study to evaluate the efficacy of the Teaching Kitchen program in Japanese patients with diabetes

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000052514
Enrollment
200
Registered
2023-11-01
Start date
2023-11-01
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Type 2 diabetes

Interventions

The program will include lectures on lifestyles and culinary trainings, and individual health coaching using wearable devices. Start the same program four month after the start of the first group

Sponsors

Graduate School of Medicine, Osaka University
Lead Sponsor
LOTTE Foundation Research Grant, KUBARA HONKE Co., Ltd., Cancer Scan. Inc.
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Age 20 to 79 2)Those who have type 2 diabetes and HbA1c 6.5% to 8.9% 3)BMI >= 23 and/or waist circumference >= 85 cm for men and >= 90 cm for women 4)Those who agree to participate in the program

Exclusion criteria

Exclusion criteria: 1)Type 1 diabetes and secondary diabetes 2)Those using rapid-acting insulin, regular insulin or premixed insulin containing them 3)Those who have been instructed by their physician to restrict protein (e.g., kidney or liver failure) 4)Those who have been instructed by their physician to limit exercise (e.g., heart failure requiring restriction of physical activity) 5)Those who are or may be pregnant or breastfeeding 6)Those with severe food allergies (anaphylactic shock) 7)Those with recent significant hypertension (systolic blood pressure >=180 mmHg or diastolic blood pressure >= 110 mmHg) 8)Those who have fasting triglycerides >=1,000 mg/dL on the most recent laboratory test 9)Those whom the principal investigator or attending physicians deems difficult to participate in the program or evaluate (e.g., physical or social factors, family objections, etc.).

Design outcomes

Primary

MeasureTime frame
Changes in HbA1c

Secondary

MeasureTime frame
Changes in lifestyles and biometrics as well as participants' satisfaction of the program

Countries

Japan

Contacts

Public ContactMegu Baden

Graduate School of Medicine, Osaka University Department of Metabolic Medicine/ Department of Lifestyle Medicine

mbaden@endmet.med.osaka-u.ac.jp06-6879-3736

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Sep 19, 2026