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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-60
SponsorInstitute for Healthier Living Abu Dhabi

About this trial

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

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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

Disqualifiers

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

Trial design

Design model

Single group

Treatments tested in this trial

  • Culinary Medicine Healthy Cooking and Home Meal Implementation Program

    Behavioral

    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.

Treatment groups

250 Participants
are divided into 1 treatment group
Group A: Culinary Medicine Intervention GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Weight Status (Body Weight)

Assessment of participant weight to determine changes associated with the culinary medicine intervention. Weight will be measured using the InBody Dial H30 portable device.

Time frame
Baseline (immediately after home cook certification and before intervention), Mid-intervention (6 weeks), and Post-intervention (3 months after intervention start).

Secondary outcomes

1

Waist Circumference

Measurement of abdominal adiposity using a smart tape according to WHO protocol.

Time frame
Baseline, 6 weeks, and 3 months.
2

Body Fat Percentage

Measurement of body fat percentage using the InBody Dial H30 portable device.

Time frame
Baseline, 6 weeks, and 3 months.
3

Blood Pressure

Systolic and diastolic blood pressure measured using a Welch Allyn ProBP 2000 device after a standardized resting period.

Time frame
Baseline, 6 weeks, and 3 months.
4

Heart Rate

Resting heart rate measured using the Welch Allyn ProBP 2000 device.

Time frame
Baseline, 6 weeks, and 3 months.

Other outcomes

1

Handgrip Strength

Measurement of muscle strength using a calibrated Jamar digital hand dynamometer. Highest value from repeated trials will be recorded.

Time frame
Baseline, 6 weeks, and 3 months.
2

Body Mass Index (BMI)

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.

Time frame
Baseline, 6 weeks, and 3 months.
3

Medication Use

Documentation of medication type and dose, including diabetes, hypertension, and weight-loss medications, to account for potential confounding effects.

Time frame
Baseline and Post-intervention (3 months).
4

Diet Quality Score

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.

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

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Institute for Healthier Living Abu Dhabi

Lead sponsor

Abu Dhabi Public Health Centre

Collaborator