- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06409962
A New Technological Intervention to Address Childhood Obesity: (NURSPEDIAOBE)
A New Technological Intervention to Address Childhood Obesity: Approach to Multidimensional Intervention
Childhood obesity is a global public health issue, with rising prevalence rates. In Spain, the problem is significant, particularly in the southern regions. Factors contributing to childhood obesity include dietary habits, lack of physical activity, and socioeconomic influences.
Efforts to address childhood obesity in Spain include various programs focusing on dietary modification, increased physical activity, and family involvement. Despite these initiatives, there is a need for continued intervention, as changing dietary and lifestyle patterns have led to reduced fruit and vegetable consumption and increased sedentary behavior among children.
Childhood obesity has concerning health implications, including heart-related issues. Echocardiography plays a vital role in early detection.
Given the limited research on the impact of childhood obesity on musculoskeletal development and mobility, a comprehensive study is needed to analyze its prevalence and associated factors. The study aims to assess the effectiveness of nutritional interventions administered by school nurses.
In summary, childhood obesity in Spain is a growing concern, with multifaceted causes and health implications. Ongoing efforts are required to combat this issue and promote healthier lifestyles among children.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
An elevated Body Mass Index (BMI) in the child population represents a significant global public health concern. According to the World Health Organization (WHO), overweight occurs in children aged 6-19 when the BMI exceeds one or more standard deviations from the median established in WHO child growth patterns.
Epidemiological data reflects that since the late 20th century, childhood obesity has increased from 4.9% (31.5 million) to 6% (40.6 million) worldwide. According to data from the Childhood Obesity Surveillance Initiative (COSI) within the European Union (EU), children in Spain aged 6-9 have a 42% overweight rate and a 19% obesity rate. In comparison, girls have a 41% overweight rate and a 17% obesity rate, positioning Spain as the fourth EU country with the highest prevalence of overweight and obesity in children.
Within the national territory, 4 out of 10 schoolchildren have excess weight, with the highest prevalence in the southern regions. The autonomous community with the lowest incidence of childhood overweight is Navarra, with 15%, and the highest is the Region of Murcia, with 40%. Andalusians present a high prevalence rate of 33.4%. In general, the country's northern regions have lower figures, while the southern region has the highest rates of childhood overweight. It has also been observed that there is a higher likelihood of being overweight in rural areas than in urban areas.
This could be due to regional differences in habits during the three critical periods for the development of childhood obesity: the preconception period involving maternal factors, the first 1000 days of life (9 months of pregnancy + 2 years of life), and the adiposity rebound between 5-7 years. Childhood overweight is also highly influenced by factors such as maternal overweight, early introduction of complementary feeding before 6 months of age, smoking during pregnancy, low parental educational levels, and the excessive use of screens such as mobile phones or tablets at an early age.
The most relevant factors in overweight are diet, physical inactivity, physical activity, and lifestyle habits. However, when it comes to minors, all these factors are strongly influenced by the cultural, social, and institutional environment, as well as the family's socioeconomic level.
In Spain, Andalusia is one of the autonomous communities with a lower income index (0.67) and a lower average expenditure on public health at 0.33%. However, the community puts in the most effort to implement policies against obesity, with a score of 5.19.
Numerous campaigns have been launched to prevent childhood obesity, developed by the Spanish Agency for Consumer Affairs, Food Safety, and Nutrition (AECOSAN) as part of the nutrition, physical activity, and obesity prevention (NAOS) strategy. Additionally, the Andalusian Ministry of Health and Families has implemented plans such as "Growing in Health," "Evaluation of Food Offer in Andalusian Schools 2019-2020," and the "Health throughout Life" campaign.
All these programs coincide on three fundamental aspects when addressing childhood obesity: interventions to modify dietary habits promoting balanced and healthy eating, increasing fruit and vegetable consumption while minimizing sugar intake; interventions to promote physical activity, encouraging at least one hour of exercise daily; and, lastly, family involvement interventions to achieve proper adherence to these changes.
These interventions are necessary today because, over the past decades, there have been changes in eating patterns and diets, resulting in a decrease in the consumption of fruits, vegetables, legumes, and fresh products, as well as an increase in the consumption of processed foods with higher sugar, fat, salt content, and poorer nutritional quality. According to COSI initiative data, Spain is where children consume the least fruits and vegetables daily. There have also been changes in physical activity, with studies showing that 25% of Spanish children are sedentary.
One of the direct consequences of childhood overweight is morphological heart alterations, reflected in left ventricular hypertrophy and cardiac diastolic alterations. Numerous scientific studies have established a close relationship between obesity in children and adolescents and an increase in epicardial fat, which can lead to cardiac and vascular abnormalities. In fact, having a high BMI at a young age has become a significant risk factor for the premature development of cardiovascular diseases that were previously considered exclusive to adults. These changes are visible through echocardiography, especially in epicardial fat.
As a non-invasive diagnostic tool, Echocardiography has gained a fundamental role in early detection of these alterations in the pediatric population affected by an increase in epicardial fat. Its early implementation allows for precise cardiac and vascular function assessment, improving these young patients' quality of life and prognosis. These measurements and modifications have been analyzed recently, although more data on younger populations and post-pandemic needs to be collected. Furthermore, to address this growing challenge, it is crucial to raise awareness about the importance of maintaining a healthy weight early and promote research and the application of preventive and intervention strategies to reduce epicardial fat in the pediatric population.
Due to all the aforementioned reasons, coupled with the limited number of current publications that deeply analyze the consequences of childhood obesity on the development of the musculoskeletal system and children's mobility, it is essential to conduct a study of the population and subsequently intervene to promote healthy growth and development in children.
Therefore, the objective is to establish the impact of a nutritional intervention by a school nurse on a group of schoolchildren.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Manuel J Guzmán Roldán, Msc
- Phone Number: 0034 957482125
- Email: jefaturadeprimaria@colegiovirgendelcarmen.com
Study Locations
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Córdoba, Spain, 14011
- Recruiting
- Colegio Virgen del Carmen
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Contact:
- Manuel Gumaz Roldan
- Email: jefaturaprimaria@virgendelcarmen.es
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Students from the school
- Pediatric from age 6 to 16
- Students from the school that confirmed approval
- Signed informed consent by the minor
- Signed informed consent by the minor's parents or guardians.
Exclusion Criteria:
- Presence of HbA1c levels below 5.7%
- Presence of HbA1c levels above 6.4%
- Presence of pathological metabolic diseases, such as diabetes or metabolic syndrome
- Presence of other diseases related to intestinal integrity or skin issues.
- Lack of the signed informed consent by the minor and legal guardian
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Technological intervention
The experimental arm integrates technology-based interventions-podcasts, gamification, and virtual reality-to promote nutritional education and healthy behaviors.
Tailored podcasts cover topics like healthy eating habits and balanced nutrition, while gamification enhances motivation.
Virtual reality offers immersive environments for exploring healthy choices.
Both experimental and control groups enable a comprehensive evaluation, collecting data through measurements, biometrics, and activity records.
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The intervention comprises workshops, individualized counseling, cooking classes, and physical activity promotion.
It emphasizes nutritional education, hands-on cooking, and behavioral modification techniques.
Participants receive personalized guidance and resources to make sustainable dietary and lifestyle changes.
Social support networks foster motivation and accountability.
By combining these components, the intervention aims to empower participants with the knowledge, skills, and support needed for long-term health improvements.
Other Names:
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No Intervention: No-technological intervention: traditional brochure
The control arm will focus on a non-technological intervention, specifically utilizing traditional brochures.
Participants in this arm will receive printed materials containing information on basic nutritional guidelines, healthy eating habits, and the importance of balanced nutrition.
The brochure-based intervention aims to provide essential information in a straightforward format, emphasizing key messages related to healthy eating practices.
Participants will have access to pamphlets outlining dietary recommendations, portion control, and tips for making nutritious food choices.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Weight (kg)
Time Frame: From 12 weeks (1st measurement) up 15th months (6th measurement)
|
Weight, as a pivotal anthropometric measure, will be quantified using a validated weight machine, alongside a body composition monitor such as the BF511.
The validated weight machine adheres to established calibration standards, ensuring precision and consistency in measurements.
It employs advanced technology to accurately assess an individual's weight in kilograms (kg), providing reliable data for scientific analyses.
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From 12 weeks (1st measurement) up 15th months (6th measurement)
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Height (m2)
Time Frame: From 12 weeks (1st measurement) up 15th months (6th measurement)
|
Height will be registered in meters squared (m^2) for its precise evaluation.
Employing a validated tachymeter, a specialized instrument designed for accurate measurements, ensures meticulous assessment of height.
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From 12 weeks (1st measurement) up 15th months (6th measurement)
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Percentage Lean Mass (LM) (%)
Time Frame: From 12 weeks (1st measurement) up 15th months (6th measurement)
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The lean fat, calculated in percentage, will be obtained using a validated weight machine, alongside a body composition monitor such as the BF511.
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From 12 weeks (1st measurement) up 15th months (6th measurement)
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Percentage Fat Mass (FM) (%)
Time Frame: 1st month, 3 month, 6 month, 9 month, 12th and 15th month
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The lean fat, calculated in percentage, will be obtained using a validated weight machine, alongside a body composition monitor such as the BF511.
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1st month, 3 month, 6 month, 9 month, 12th and 15th month
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Body Mass Index (kg/m2)
Time Frame: From 12 weeks (1st measurement) up 15th months (6th measurement)
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The Body Mass Index will be calculated using the percentiles according to age group and sex.
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From 12 weeks (1st measurement) up 15th months (6th measurement)
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Waist circumference (cm)
Time Frame: From 12 weeks (1st measurement) up 15th months (6th measurement)
|
The waist circumference (cm) of the children will be measured via an inextensible measuring tape at the initial visit (1st month or V0) and at the last visit (15th month or V6).The measurement follows the recommendations of the International Standards for Anthropometric Assessment
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From 12 weeks (1st measurement) up 15th months (6th measurement)
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Hip circumference(cm)
Time Frame: From 12 weeks (1st measurement) up 15th months (6th measurement)
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The Hip circumference(cm) of the children will be measured via an inextensible measuring tape at the initial visit (1st month or V0) and at the last visit (15th month or V6).The measurement follows the recommendations of the International Standards for Anthropometric Assessment
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From 12 weeks (1st measurement) up 15th months (6th measurement)
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Arm circumference (cm)
Time Frame: From 12 weeks (1st measurement) up 15th months (6th measurement)
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The arm circumference (cm) of the children will be measured via an inextensible measuring tape at the initial visit (1st month or V0) and at the last visit (15th month or V6).The measurement follows the recommendations of the International Standards for Anthropometric Assessment
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From 12 weeks (1st measurement) up 15th months (6th measurement)
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Calf circumference (cm)
Time Frame: From 12 weeks (1st measurement) up 15th months (6th measurement)
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The arm circumference (cm) of the children will be measured via an inextensible measuring tape at the initial visit (1st month or V0) and at the last visit (15th month or V6).The measurement follows the recommendations of the International Standards for Anthropometric Assessment
|
From 12 weeks (1st measurement) up 15th months (6th measurement)
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Validated nutritional assessment questionnaire: adherence to the Mediterranean diet (KIDMED)
Time Frame: From 12 weeks (1st measurement) up 15th months (6th measurement)
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he KIDMED will be used to determine adherence to the change in diet from the initial visit (V0) and the final visit (V6).
This questionnaire is formed by 16 questions related to adherence to the Mediterranean diet, in addition to 7 items complementary to the test.
All questions were answered positively or negatively.
Of the 16 main questions, questions number 6, 11, 14, and 16, in their affirmative answers had a negative meaning, so they were worth (-1), on the other hand, the remaining questions whose affirmative answers represented a positive value concerning the Mediterranean diet were scored with (+1).
Negative responses do not score (0).
According to the test, the results are grouped into different levels of adherence to the Mediterranean diet, low (score 0 to 3), medium (score 4-7), and high (8 to 12).
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From 12 weeks (1st measurement) up 15th months (6th measurement)
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Food Consumption Frequency
Time Frame: From 12 weeks (1st measurement) up 15th months (6th measurement)
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Food Frequency Questionnaire (FFQ) will be used to determine the consumption of food and the change in diet from the initial visit (V0) and the final visit (V6). Energy and nutrient intakes were calculated using Spanish food composition tables Food consumption frequency refers to the rate at which individuals consume different types of food within a specific time frame, typically measured over a day, week, or month. This variable captures the frequency with which individuals consume various food groups, such as fruits, vegetables, grains, proteins, and processed foods. It provides insight into dietary patterns and habits, indicating how often individuals incorporate different foods into their regular eating routines. |
From 12 weeks (1st measurement) up 15th months (6th measurement)
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Blood pressure
Time Frame: From 12 weeks (1st measurement) up 15th months (6th measurement)
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The systolic and diastolic blood pressure will be taken using an Omron-validated tensiometer with two measurements between 15 minutes each measurement from the 1st visit (v0) to the last (v6).
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From 12 weeks (1st measurement) up 15th months (6th measurement)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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3D avatar system for anthropometric measures
Time Frame: From 12 weeks (1st measurement) up 15th months (6th measurement)
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The validation of avatar systems based on artificial vision involves assessing the accuracy, reliability, and effectiveness of virtual representations controlled by artificial intelligence algorithms. These avatars, generated using artificial vision technology, mimic human-like behavior and interactions within virtual environments. Validation encompasses rigorous testing to ensure that avatars accurately interpret and respond to visual inputs, such as facial expressions or gestures, in a manner consistent with human perception. The validation of avatar systems based on artificial vision involves assessing the accuracy, reliability, and effectiveness of virtual representations controlled by artificial intelligence algorithms. The results of the model will provide, using the height and weight previously measured with the Body Composition validated weight scale, will be obtained the arm, waist, calf and arm circumferences. |
From 12 weeks (1st measurement) up 15th months (6th measurement)
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: Manuel Vaquero Abellan, MD, Msc, PhD, Universidad de Córdoba
- Principal Investigator: Manuel Vaquero Alvárez, MD, Msc, PhD, Maimónides Biomedical Research Institute of Córdoba
- Principal Investigator: Isabel Blancas Sanchez, MD, Msc, PhD, Primary Care, Jaen
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 5345
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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