Evaluation of a Structured Nutrition Educational Program Among Patients With Type 2 Diabetes
17 de mayo de 2026 actualizado por: Ly Na Dau, Cho Ray Hospital
Evaluation of a Structured Nutrition Education Program for Patients With Type 2 Diabetes Who Have Not Achieved Glycemic Goals Under Oral Anti-diabetic Medications or in Combination With Basal Insulin in Vietnam
The purpose of this study is to find out if learning about healthy eating can help people with diabetes control their blood sugar better.
This study is for men and women between 16 and 70 years old who currently use only oral-diabetic medications or in combination with basal insulin but their glycemia have not been in the target range.
The investigators want to answer the following questions:
Can nutrition education help lower HbA1c (a blood test that shows average blood sugar over the past 3 months)? Can it improve nutrition related knowledge, attitude and behaviors among patients with type 2 diabetes? Will it help reduce fasting blood sugar, lipid levels, body weight, and the number of times low blood sugar (hypoglycemia) happens?
Participants will be divided into two groups:
One group will receive a nutrition booklet. The other group will receive the same booklet and join four monthly lessons with a researcher.
The four lessons will talk about:
Goals for managing diabetes Main nutrients in food and their effects on glycemia How to plan meals How to eat in a way that supports better blood sugar control
Descripción general del estudio
Estado
Aún no reclutando
Condiciones
Intervención / Tratamiento
Descripción detallada
This study will involve 253 people with diabetes who currently uses only oral anti-diabetic medications or in combination with basal insulin without their glycemia within the target range.
The study will take place at Cho Ray Hospital in Ho Chi Minh City, Vietnam, and will run from 2026 to 2027. People will be invited to join at the Endocrinology Consultation Unit. If they agree, their phone number will be collected and the research team will call them later to explain more about the study. If they are still interested, a meeting with the researcher will be planned on the day of their next consultation. During this meeting, the patients will be screened for their eligibility.
On the screening day, the patients will have their blood tests to check their sugar, HbA1c, cholesterol, and kidney function as part of their routine visit and have a usual consultation with their doctor. If the patients meet all the criteria and agree to take part in, the patients will sign the consent form and take short tests on nutrition related knowledge, attitude, and behavior questionnaire designed and evaluated by the researcher.
After that, the patients will be randomly assigned to one of two groups. One group will get a nutrition booklet only. The other group will receive the booklet plus attend four monthly sessions with a researcher to learn about healthy eating for diabetes.
During the 6-month study period, all participants will have blood tests every 3 months to check HbA1c, fasting sugar, and lipid; the participants will be asked monthly about any low blood sugar episodes; their weight and waist size will be measured every 3 months, and their height will be measured at the start of the study. The participants will be interviewed with the nutrition related knowledge-attitude-behavior questionnaire again after 6 months.
Tipo de estudio
Intervencionista
Inscripción (Estimado)
253
Fase
- No aplica
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Estudio Contacto
- Nombre: Na Ly Dau, MD
- Número de teléfono: +49379942392
- Correo electrónico: Ly.Dau@lrz.uni-muenchen.de
Ubicaciones de estudio
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Ho Chi Minh City, Vietnam, 700000
- Cho Ray Hospital
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Contacto:
- Na Ly Dau, MD
- Número de teléfono: +49379942392
- Correo electrónico: Ly.Dau@lrz.uni-muenchen.de
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Investigador principal:
- Na Ly Dau, MD
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Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
- Niño
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
No
Descripción
Inclusion Criteria:
- People between 16 and 70 years old.
- People who come to Cho Ray Hospital for diabetes care and plan to keep getting care there for at least six months.
- People who have diabetes and have been prescribed diabetes medicine.
- People who were recently diagnosed with diabetes, based on the latest guidelines from the American Diabetes Association.
- People whose blood sugar (HbA1c) level is higher than 7.5 %.
- People who are currently using only oral anti-diabetic medications or in combination with basal insulin
Exclusion Criteria:
- People who are seriously ill and need to stay in the hospital, such as those with infections, pneumonia, heart attacks, strokes, or infected diabetic foot.
- People who have cancer, serious mental health problems, or problems with drug use.
- People who do not want to take part or cannot follow the study plan.
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
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Sin intervención: Standard group
The participants of this group will be given a nutrition booklet and follow the standard of care, which means the participants routinely have about 5 to 10-minute consultations with their doctors.
During this time, the participants tell their doctors about how they feel physically, their doctors then examine the patients, educate them if necessary, and prescribe the tests and medications.
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Experimental: Nutrition Intervention group
Participants in the intervention group will attend a structured nutrition education program consisting of four monthly sessions, each lasting approximately 40 to 60 minutes.
These sessions will be conducted in small groups by the researcher.
Each session includes: A 20-minute presentation delivered by the researcher using visual aids, such as slides and educational images, a 15-minute Q and A section, and 20 minutes of working on group assignments.
Session Topics: Treatment Goals in Diabetes Care: Overview of blood glucose targets and the importance of achieving glycemic control.
Key Nutritional Components of Food: Roles of carbohydrates, proteins, fats, fiber, and their impact on blood glucose.
Principles of Meal Planning: Adjusting energy intake based on physical activity levels and BMI.
Understanding the Food Exchange System: Introduction to food exchange lists; selecting the appropriate number of food exchanges.
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Experimental: Nutrition intervention group Arm Description: Participants in the intervention group will attend a structured nutrition education program consisting of four monthly sessions, each lasting approximately 40 to 60 minutes.
These sessions will be conducted in small groups by the researcher.
Each session includes: A 20-minute presentation delivered by the researcher using visual aids, such as slides and educational images, a 15-minute Q and A section, and 20 minutes of working on group assignments.
Session Topics: Treatment Goals in Diabetes Care: Overview of blood glucose targets and the importance of achieving glycemic control.
Key Nutritional Components of Food: Roles of carbohydrates, proteins, fats, fiber, and their impact on blood glucose.
Principles of Meal Planning: Adjusting energy intake based on physical activity levels and BMI.
Understanding the Food Exchange System: Introduction to food exchange lists; selecting the appropriate number of food exchanges.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Change in Hba1c (%) from baseline to 6 months, comparing intervention vs control
Periodo de tiempo: 6 months
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the change in Hba1c (%) from the baseline to 6 months, comparing intervention vs standard group
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6 months
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Change in HbA1c (%) from baseline to 3 months, comparing intervention vs control
Periodo de tiempo: 3 months
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Change in HbA1c (%) from baseline to 3 months, comparing intervention vs standard group
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3 months
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Change in BMI from baseline to 3 months and 6 months, comparing the intervention vs control
Periodo de tiempo: 3 months and 6 months
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Change in BMI from baseline to 3 months and 6 months, comparing the intervention vs standard group
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3 months and 6 months
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Differences of total daily insulin dose after 3 months and after 6 months, comparing the intervention vs control
Periodo de tiempo: 3 months and 6 months
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Differences of total daily insulin dose after 3 months and after 6 months, comparing the intervention vs standard groups
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3 months and 6 months
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Difference of number of distinct anti-diabetic medication classes used per day after 3 months, and after 6 months, comparing the intervention vs control
Periodo de tiempo: 3 months, and 6 months
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Difference of number of distinct anti-diabetic medication classes used per day after 3 months, and after 6 months, comparing the intervention vs standard group
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3 months, and 6 months
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Differences in daily doses of each oral anti-diabetic medication and dyslipidemia medication after 3 months, and after 6 months, comparing the intervention vs control
Periodo de tiempo: 3 months, and 6 months
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Differences in daily doses of each oral anti-diabetic medication and dyslipidemia medication after 3 months, and after 6 months, comparing the intervention vs standard group
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3 months, and 6 months
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Changes in nutrition-related knowledge, attitude and behavior score from baseline to 6 months, comparing the intervention vs control
Periodo de tiempo: 6 months
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Changes in nutrition-related knowledge, attitude and behavior score from baseline to 6 months, comparing the intervention vs standard group
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6 months
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Difference in possible self-reported hypoglycemia episodes recorded in the previous month from baseline to 3 months, and to 6 months, comparing the intervention vs control
Periodo de tiempo: 3 months and 6 months
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Difference in possible self-reported hypoglycemia episodes recorded in the previous month from baseline to 3 months, and to 6 months, comparing the intervention vs standard group
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3 months and 6 months
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Change in waist circumference from baseline to 3 months and 6 months, comparing the intervention vs control
Periodo de tiempo: 3 months and 6 months
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Change in waist circumference from baseline to 3 months and 6 months, comparing the intervention vs standard group
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3 months and 6 months
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Change in fasting blood glucose from baseline to 3 months and 6 months, comparing the intervention vs control
Periodo de tiempo: 3 months and 6 months
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Change in fasting blood glucose from baseline to 3 months and 6 months, comparing the intervention vs standard group
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3 months and 6 months
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Change in LDL cholesterol from baseline to 3 months and 6 months, comparing the intervention vs control
Periodo de tiempo: 3 months and 6 months
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Change in LDL cholesterol from baseline to 3 months and 6 months, comparing the intervention vs standard group
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3 months and 6 months
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Change in Total triglyceride from baseline to 3 months and 6 months, comparing the intervention vs control
Periodo de tiempo: 3 months and 6 months
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Change in Total triglyceride from baseline to 3 months and 6 months, comparing the intervention vs standard group
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3 months and 6 months
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Change in total cholesterol from baseline to 3 months and 6 months, comparing the intervention vs control
Periodo de tiempo: 3 months and 6 months
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Change in total cholesterol from baseline to 3 months and 6 months, comparing the intervention vs standard group
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3 months and 6 months
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Change in HDL cholesterol from baseline to 3 months and 6 months, comparing the intervention vs control
Periodo de tiempo: 3 months and 6 months
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Change in HDL cholesterol from baseline to 3 months and 6 months, comparing the intervention vs standard group
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3 months and 6 months
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Differences of daily number of insulin injections after 3 months and after 6 months, comparing the intervention vs control
Periodo de tiempo: 3 months and 6 months
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Differences of daily number of insulin injections after 3 months and after 6 months, comparing the intervention vs standard groups
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3 months and 6 months
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Differences of total daily slow-acting insulin dose after 3 months and after 6 months, comparing the intervention vs control
Periodo de tiempo: 3 months and 6 months
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Differences of total daily slow-acting insulin dose after 3 months and after 6 months, comparing the intervention vs standard groups
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3 months and 6 months
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Differences of total daily fast-acting insulin dose after 3 months and after 6 months, comparing the intervention vs control
Periodo de tiempo: 3 months and 6 months
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Differences of total daily fast-acting insulin dose after 3 months and after 6 months, comparing the intervention vs standard groups
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3 months and 6 months
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Otras medidas de resultado
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Difference in cost-effectiveness ratios (monthly per-patient cost for diabetic care per unit of improvement in glycemic control) after six months, comparing the intervention vs control.
Periodo de tiempo: 6 months
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Difference in cost-effectiveness ratios (monthly per-patient cost for diabetic care per unit of improvement in glycemic control) after six months, comparing the intervention vs standard group.
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6 months
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Na Ly Dau, MD, Cho Ray Hospital
Publicaciones y enlaces útiles
La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.
Publicaciones Generales
- Davies MJ, Aroda VR, Collins BS, Gabbay RA, Green J, Maruthur NM, Rosas SE, Del Prato S, Mathieu C, Mingrone G, Rossing P, Tankova T, Tsapas A, Buse JB. Management of Hyperglycemia in Type 2 Diabetes, 2022. A Consensus Report by the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD). Diabetes Care. 2022 Nov 1;45(11):2753-2786. doi: 10.2337/dci22-0034.
- Franz MJ, MacLeod J, Evert A, Brown C, Gradwell E, Handu D, Reppert A, Robinson M. Academy of Nutrition and Dietetics Nutrition Practice Guideline for Type 1 and Type 2 Diabetes in Adults: Systematic Review of Evidence for Medical Nutrition Therapy Effectiveness and Recommendations for Integration into the Nutrition Care Process. J Acad Nutr Diet. 2017 Oct;117(10):1659-1679. doi: 10.1016/j.jand.2017.03.022. Epub 2017 May 19. No abstract available.
- Subhan FB, Fernando DN, Thorlakson J, Chan CB. Dietary Interventions for Type 2 Diabetes in South Asian Populations-A Systematic Review. Curr Nutr Rep. 2023 Mar;12(1):39-55. doi: 10.1007/s13668-022-00446-9. Epub 2022 Nov 29.
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Estimado)
1 de junio de 2026
Finalización primaria (Estimado)
30 de abril de 2027
Finalización del estudio (Estimado)
30 de abril de 2027
Fechas de registro del estudio
Enviado por primera vez
19 de abril de 2026
Primero enviado que cumplió con los criterios de control de calidad
17 de mayo de 2026
Publicado por primera vez (Actual)
20 de mayo de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
20 de mayo de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
17 de mayo de 2026
Última verificación
1 de febrero de 2026
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- ChoRay_OMIN_2026
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
SÍ
Descripción del plan IPD
All the outcome-related data collected from the participant, which were described in the study protocol, will be shared.
The data, which involves participants' identities or can be used to track their identities, will not be shared.
The shared data will be published on a website that specializes in the data management chosen by the principal investigator.
Criterios de acceso compartido de IPD
The public will be able to access the IPD and supporting information; they need to log into the website.
All the shared information will be available to the public
Tipo de información de apoyo para compartir IPD
- PROTOCOLO DE ESTUDIO
- SAVIA
- CIF
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .