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Cooking Classes as a Family-based Intervention for Weight Reduction: Effects on Dietary Quality and Weight Management in Abu Dhabi (United Arab Emirates)

17 de julio de 2026 actualizado por: Institute for Healthier Living Abu Dhabi

The goal of this quasi-experimental interventional study is to learn if healthy cooking classes for home cooks can improve weight management and dietary quality among Emirati adults with overweight or obesity living in Abu Dhabi. The main questions it aims to answer are:

  • Does participation in the culinary medicine program reduce body weight over time?
  • Does the intervention improve diet quality and increase compliance with healthy home-cooked meals?
  • Does the intervention improve health measures such as waist circumference, body fat percentage, blood pressure, and heart rate?
  • What are the experiences and satisfaction levels of participating family members and trained home cooks?

Participants will:

  • Enroll in a 3-month family-based nutrition intervention program
  • Receive meals prepared by home cooks trained in culinary medicine through the ICCA program
  • Complete assessments before the intervention, during the intervention, and 3 months after completion
  • Undergo measurements including weight, waist circumference, body fat percentage, blood pressure, and heart rate
  • Complete questionnaires about diet quality, meal habits, and overall program experience

Descripción general del estudio

Tipo de estudio

Intervencionista

Inscripción (Estimado)

250

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: Erik Koornneef, Ph.D
  • Número de teléfono: +971500888594
  • Correo electrónico: e.koornneef@ihlad.ae

Copia de seguridad de contactos de estudio

  • Nombre: Yamna Azim
  • Número de teléfono: +971509149171
  • Correo electrónico: y.azim@ihlad.ae

Ubicaciones de estudio

      • Abu Dhabi, Emiratos Árabes Unidos
        • Reclutamiento
        • Institute for Healthier Living Abu Dhabi
        • Contacto:

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

  • Adulto

Acepta Voluntarios Saludables

Sí

Descripción

Inclusion Criteria:

  • Emirati
  • Based in Abu Dhabi
  • Home cooked meals prepared by full-time home cooks who are certified in the ICCA Culinary Medicine course (post 4 weeks cooking training)
  • Certified home cooks are residing with participant during the training and intervention
  • Aged between 18 years and 60 years
  • BMI between 28-40 kg/m2
  • Participant and cooks being able to provide informed consent

Exclusion Criteria:

  • Body weight exceeding 220 kilograms at the time of recruitment
  • Undergoing treatment for serious illnesses (active cancer), planned for surgery, interventional management, and immunomodulation
  • Undergone surgery within 3 months prior to study recruitment, including bariatric surgery
  • Enrolled in other lifestyle intervention programs

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: Prevención
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Culinary Medicine Intervention Group
Participants receive a household-based culinary medicine intervention. The designated home cook undergoes a 4-week ICCA culinary medicine training program focused on healthy cooking techniques, nutrition education, and chronic disease prevention. Following training, the home cook implements healthy home-prepared meals for participating household members over a 3-month period. Participants receive repeated assessments of weight, anthropometric measures, blood pressure, heart rate, body composition, and diet quality at baseline, mid-intervention (6 weeks), and post-intervention (3 months).
This intervention consists of a 4-week structured culinary medicine training program delivered by ICCA to designated household home cooks. The training includes theoretical nutrition education and practical cooking sessions focused on healthy meal preparation techniques aimed at reducing chronic disease risk. Following completion of training and certification, home cooks implement these techniques over a 3-month period by preparing and providing healthy home-cooked meals for participating household members. The intervention encourages reduced reliance on ultra-processed and restaurant foods and promotes improved dietary quality, with outcomes assessed through repeated measures of anthropometry, body composition, cardiovascular indicators, and dietary intake.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Weight Status (Body Weight)
Periodo de tiempo: Baseline (immediately after home cook certification and before intervention), Mid-intervention (6 weeks), and Post-intervention (3 months after intervention start).
Assessment of participant weight to determine changes associated with the culinary medicine intervention. Weight will be measured using the InBody Dial H30 portable device.
Baseline (immediately after home cook certification and before intervention), Mid-intervention (6 weeks), and Post-intervention (3 months after intervention start).

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Waist Circumference
Periodo de tiempo: Baseline, 6 weeks, and 3 months.
Measurement of abdominal adiposity using a smart tape according to WHO protocol.
Baseline, 6 weeks, and 3 months.
Body Fat Percentage
Periodo de tiempo: Baseline, 6 weeks, and 3 months.
Measurement of body fat percentage using the InBody Dial H30 portable device.
Baseline, 6 weeks, and 3 months.
Blood Pressure
Periodo de tiempo: Baseline, 6 weeks, and 3 months.
Systolic and diastolic blood pressure measured using a Welch Allyn ProBP 2000 device after a standardized resting period.
Baseline, 6 weeks, and 3 months.
Heart Rate
Periodo de tiempo: Baseline, 6 weeks, and 3 months.
Resting heart rate measured using the Welch Allyn ProBP 2000 device.
Baseline, 6 weeks, and 3 months.
Compliance with Home-Cooked Meal Consumption
Periodo de tiempo: Every week for 3 months
Survey-based assessment of participant adherence to consuming meals prepared by the trained home cook
Every week for 3 months
Frequency of home-cooked meal consumption.
Periodo de tiempo: every week for 3 months
Number of home-cooked meals consumed per week, assessed by participant survey.
every week for 3 months
Participant Experience and Satisfaction
Periodo de tiempo: End of intervention (3 months).
Survey evaluating participants' overall experience, satisfaction, acceptability, and perceived benefits of the culinary medicine program.
End of intervention (3 months).

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Handgrip Strength
Periodo de tiempo: Baseline, 6 weeks, and 3 months.
Measurement of muscle strength using a calibrated Jamar digital hand dynamometer. Highest value from repeated trials will be recorded.
Baseline, 6 weeks, and 3 months.
Body Mass Index (BMI)
Periodo de tiempo: Baseline, 6 weeks, and 3 months.
BMI calculated using measurements obtained from the InBody Dial H30 and height from the SECA stadiometer. Although weight is the primary outcome, BMI is also collected and may be analyzed.
Baseline, 6 weeks, and 3 months.
Medication Use
Periodo de tiempo: Baseline and Post-intervention (3 months).
Documentation of medication type and dose, including diabetes, hypertension, and weight-loss medications, to account for potential confounding effects.
Baseline and Post-intervention (3 months).
Diet Quality Score
Periodo de tiempo: Pre-intervention (during recruitment/consent) and Post-intervention (end of 3-month intervention).

Assessment of dietary quality using the Global Diet Quality Questionnaire (GDQS), including overall score and NCD-Risk/NCD-Protect indicators. The following summarizes the scoring system of the GDQS:

Score Range Interpretation

- GDS (Global Diet Score / GDR Score): (0-18) Overall diet quality score combining protective and risk components. Higher scores indicate better adherence to global dietary recommendations.

NCD-Protect: (0-9) Measures consumption of foods that protect against non-communicable diseases (e.g., fruits, vegetables, whole grains, pulses, nuts, seeds). Higher scores are better.

NCD-Risk: (0-9) Measures consumption of foods associated with increased NCD risk (e.g., processed meat, sugary foods and beverages, ultra-processed salty foods). Higher scores indicate greater dietary risk.

Pre-intervention (during recruitment/consent) and Post-intervention (end of 3-month intervention).

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

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

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 (Actual)

8 de octubre de 2025

Finalización primaria (Estimado)

30 de septiembre de 2026

Finalización del estudio (Estimado)

31 de octubre de 2026

Fechas de registro del estudio

Enviado por primera vez

11 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

29 de junio de 2026

Publicado por primera vez (Actual)

30 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

20 de julio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

17 de julio de 2026

Última verificación

1 de julio de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

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. .

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