Institute for Healthier Living Abu Dhabi
Abu Dhabi, United Arab Emirates
Location status: Recruiting
NCT Number: NCT07675148
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
Interested in participating?
Request Info18 year–60 year
All sexes
Interventional
Not applicable
Abu Dhabi, United Arab Emirates
Location status: Recruiting
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
Time frame: 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.
Time frame: Baseline, 6 weeks, and 3 months.
Measurement of abdominal adiposity using a smart tape according to WHO protocol.
Time frame: Baseline, 6 weeks, and 3 months.
Measurement of body fat percentage using the InBody Dial H30 portable device.
Time frame: Baseline, 6 weeks, and 3 months.
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.
Resting heart rate measured using the Welch Allyn ProBP 2000 device.
Time frame: Every week for 3 months
Survey-based assessment of participant adherence to consuming meals prepared by the trained home cook
Time frame: every week for 3 months
Number of home-cooked meals consumed per week, assessed by participant survey.
Time frame: End of intervention (3 months).
Survey evaluating participants' overall experience, satisfaction, acceptability, and perceived benefits of the culinary medicine program.
Time frame: 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.
Time frame: 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.
Time frame: 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.
Time frame: 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
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.
Contact information is provided by the study sponsor or research team.
Erik Koornneef, Ph.D
CONTACT
Yamna Azim
CONTACT
Institute for Healthier Living Abu Dhabi
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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