- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT07519122
Fangshan Active Nutrition Initiative (FAN)
Badania nad zarządzaniem masą ciała dzieci w wieku szkolnym w Dzielnicy Fangshan z wykorzystaniem cyfrowej platformy inteligentnej
The goal of this study is to evaluate the effectiveness of a school-based weight management intervention delivered through a digital platform (WeChat) in preventing excessive weight gain and improving health behaviors in school-aged children in Fangshan District, Beijing. The main questions it aims to answer are:
Does the intervention group show a significantly lower mean increase in BMI, body fat percentage, and waist circumference compared to the control group? Does the intervention group show a significantly lower obesity rate and new obesity incidence compared to the control group? Does the intervention group show significant improvements in healthy eating, sedentary behavior, sleep, physical activity, and physical fitness test scores compared to the control group? Researchers will compare children in intervention schools (who receive the multi-level intervention targeting students, families, and schools, supported by a digital platform for behavior monitoring and feedback) to children in control schools (who do not receive the intervention during the study period).
Participants in the intervention group will: (1) attend 10 student health education sessions; (2) have their physical activity at school increased to 60 minutes/day of moderate-to-vigorous activity; (3) have parents attend health education lectures and use a WeChat platform to receive health information, log child health data, and receive automated feedback; (4) have their height, weight, waist circumference, and body composition measured monthly by school health staff; and (5) be followed with assessments at 6, 12, and 24 months.
Przegląd badań
Status
Warunki
Interwencja / Leczenie
Szczegółowy opis
Study Design This is a two-arm, cluster-randomized controlled trial (cRCT) designed to evaluate the implementation and effectiveness of a multi-level, digital platform-based weight management intervention for school-aged children in Fangshan District, Beijing. The study consists of a 12-month active intervention period followed by an additional 12 months of follow-up, totaling 24 months of observation post-baseline.
Setting and Participants The study will be conducted in 10 primary schools in Fangshan District, Beijing, recruited through the Fangshan District School Health Care Center. Schools will be randomized (1:1 ratio) to either the intervention or control arm. Participants will be third-grade students (aged 8-9 years) at baseline.
Inclusion Criteria: Eligible students must provide signed informed consent from a parent or guardian and their own assent.
Exclusion Criteria: Students with pre-existing medical conditions that contraindicate physical activity or secondary obesity of known endocrine origin will be excluded from the analytic sample but may participate in the general program activities to avoid exclusion-based stigma.
InterventionThe intervention targets three levels-students, families, and schools-over one academic year. A digital platform embedded within WeChat serves as the central hub for knowledge dissemination, behavior monitoring, and automated feedback.
-
Student-level Interventions Health Education: Ten 40-minute classroom sessions delivered every 2-3 weeks, focusing on healthy weight maintenance, reducing sugar-sweetened beverages (SSBs), limiting sedentary behavior, and increasing physical activity. Sessions include interactive "hand-in-hand" homework assignments to be completed with parents.
Physical Activity Promotion: Targeted daily routines to achieve at least 60 minutes of moderate-to-vigorous physical activity (MVPA) at school, emphasizing outdoor activities and muscle/bone-strengthening exercises.
Monitoring: Monthly anthropometric measurements (height, weight, waist circumference, and body composition) conducted by trained school health staff, supplemented by weekly student self-weighing using classroom scales.
-
Family-level Interventions Parental Education: Two health education seminars per academic year (30-40 minutes each) and optional parent discussion forums to address implementation challenges.
Digital Engagement: Parents use the WeChat platform to: (a) receive regular push notifications of health education materials, (b) complete monthly behavioral questionnaires (diet, activity, sleep), and (c) view individualized monthly feedback reports comparing their child's BMI and behavioral progress against health standards.
Home Environment: Encouragement of home-based active play and parental modeling of healthy habits.
-
School-level Interventions Coordination: Designation of a school-level project coordinator to oversee logistics.
Environmental Changes: Integration of health sessions into the formal timetable and implementation of policies to limit the availability and consumption of SSBs and unhealthy snacks on campus.
Atmosphere: Classroom-based health promotion materials (e.g., posters, food environment labeling) and professional development for involved teachers.
Control Group Control schools will maintain their usual curriculum during the 12-month intervention period. Following the 24-month follow-up assessment, control schools will be provided with the intervention curriculum and relevant health education resources as an ethical cross-over.
Follow-Up and Data Collection Assessments will be conducted at baseline, 6 months, 12 months, and 24 months. Anthropometric & Clinical: Height, weight, waist/hip circumference, blood pressure, and body fat percentage (via bioelectrical impedance analysis).
Physical Fitness: 1-minute rope skipping, 1-minute sit-ups, standing long jump, and endurance shuttle runs.
Questionnaires: Validated tools for students and parents assessing dietary habits, physical activity, sedentary time, and sleep quality.
Statistical Analysis and Sample Size Sample Size: Assuming a mean BMI reduction of 0.50 kg/m2 (SD: 1.40kg/m2), an intra-cluster correlation coefficient (ICC) of 0.03, and a two-sided significance level of 0.05. Accounting for a 10% attrition rate, a total of 135 students per school is required. With 10 schools (4 classes per school, approximately 35 students per class), the study targets a total sample of approximately 1,400 students, achieving 80% power.
Evaluation: Mixed-effects models will be used to analyze primary and secondary outcomes, accounting for school-level clustering and repeated measures.
Ethical Considerations The protocol and all materials have been approved by the Institutional Review Board of Peking University Health Science Center. Participation is strictly voluntary. Personal data will be anonymized, and protocols include specific measures to avoid weight-based stigma and ensure privacy during physical assessments.
Study Timeline Recruitment & Baseline: March 2026 Active Intervention: March 2026 - March 2027 Follow-up Assessments: September 2026 (6m), March 2027 (12m), and March 2028 (24m) Analysis & Publication: March 2027 - June 2028
Typ studiów
Zapisy (Szacowany)
Faza
- Nie dotyczy
Kontakty i lokalizacje
Kontakt w sprawie studiów
- Nazwa: Chunjie Yin, PhD
- Numer telefonu: +86 15652217112
- E-mail: yinchunjie@bjmu.edu.cn
Lokalizacje studiów
-
-
-
Beijing, Chiny
- Peking University Health Science Center
-
-
Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion Criteria:
- Schools will be selected based on the consent of primary leadership, demonstrated cooperation, and availability of necessary personnel (e.g., school health professionals).
- Classes will be limited to grades 2 and 3, with teachers showing strong willingness to collaborate.
- Both parental informed consent and child assent are required for participation.
Exclusion Criteria:
- Schools will be excluded if they cater to special populations (e.g., schools for children with disabilities), are involved in other obesity-related interventions within the specified timeframe, or plan to close or relocate within two years.
- Children will be excluded if they have histories of major organ diseases (e.g., cardiac, pulmonary, hepatic, or renal conditions), special diets (e.g., vegetarian), pathological eating disorders, physical limitations affecting activity, or obesity due to endocrine disorders or medication side effects.
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Zapobieganie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Pojedynczy
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
|
Eksperymentalny: A multi-level collaborative intervention
Participants in this arm will receive a 12-month multi-level weight management intervention delivered via a digital intelligence platform (embedded in WeChat). The intervention targets three levels: Student level: 10 bi-weekly health education sessions and daily promotion of 60-minute moderate-to-vigorous physical activity (MVPA). Family level: Two parental seminars and access to the digital platform for health education "push" notifications, behavioral monitoring (diet, sleep, activity), and automated monthly BMI feedback reports. School level: Environmental changes including healthy school policies (limiting sugar-sweetened beverages), health promotion materials (posters), and teacher training. Monthly anthropometric measurements and weekly self-weighing will be conducted to monitor progress. |
This multi-level behavioral intervention integrates digital technology with school-based health promotion to address childhood obesity. Key components include: Digital Hub: A WeChat-embedded platform for real-time behavior monitoring (diet, physical activity, sleep) and automated monthly feedback reports for parents. Structured Curriculum: Ten 40-minute health education sessions for students delivered every 2-3 weeks, complemented by interactive "hand-in-hand" homework assignments. Physical Activity: Daily school-based promotion to ensure ≥60 minutes of MVPA, emphasizing outdoor and resistance exercises. Environmental Policy: Implementation of school-wide restrictions on sugar-sweetened beverages (SSBs) and unhealthy snacks. Parental Engagement: Two dedicated health seminars and regular push notifications of evidence-based health tips via the digital platform. The intervention is distinguished by its multi-sectoral approach (connecting students, parents, and school staff) and it |
|
Brak interwencji: usual-care control
Participants in this arm will follow the standard school curriculum and health education as mandated by the local education authority. They will not have access to the digital weight management platform or the specific intervention modules during the 12-month active study period. To ensure ethical standards, control schools will receive the intervention materials and resources after the completion of the 24-month follow-up assessment (wait-list control design). Baseline and follow-up data collection (anthropometric measurements and questionnaires) will be conducted at the same intervals as the intervention group. |
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Children's BMl change
Ramy czasowe: at the end of the 12-month intervention
|
Calculated based on height and weight using WHO standards. The primary outcome is the difference between two arms in the change of children's BMI from baseline to the end of the follow-up |
at the end of the 12-month intervention
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Children's Eating Behaviors
Ramy czasowe: at the end of the 12-month intervention
|
Assessed using the Children's Eating Behavior Questionnaire (CEBO), measuring dimensions such as food responsiveness satiety responsiveness, and emotional eating |
at the end of the 12-month intervention
|
|
body fat percent (BFP)
Ramy czasowe: at the end of the 12-month intervention; at 24-month follow-up
|
BFP were measured via bioelectrical impedance analysis (Tanita MC 780 MA) |
at the end of the 12-month intervention; at 24-month follow-up
|
|
Prevalence of Obesity among School-aged Children
Ramy czasowe: at the end of the 12-month intervention; at 24-month follow-up
|
The percentage of students classified as obese based on Age- and Sex-specific Body Mass Index (BMI) criteria. |
at the end of the 12-month intervention; at 24-month follow-up
|
|
Body Mass Index Z-score(BMI-z)
Ramy czasowe: at the end of the 12-month intervention; at 24-month follow-up
|
The BMI-z score is calculated based on height and weight using WHO standards |
at the end of the 12-month intervention; at 24-month follow-up
|
|
Waist Circumference
Ramy czasowe: at the end of the 12-month intervention; at 24-month follow-up
|
Waist circumference is measured at the midpoint between the lower margin of the last palpable rib and the top of the iliac crest to evaluate central adiposity |
at the end of the 12-month intervention; at 24-month follow-up
|
|
Time Spent in Physical Activity
Ramy czasowe: at the end of the 12-month intervention
|
Evaluated using the Children's Leisure Activities Study Survey (CLAss), assessing the amount and type of physical activity and sedentary behavior, including screen time |
at the end of the 12-month intervention
|
|
Time Spent in Sedentary Behavior
Ramy czasowe: at the end of the 12-month interventionl
|
Evaluated using the chidren's Leisure Activities Study survey (CLAss), assessing the amount and type of physical activity and sedentary behavior,includingscreen time. |
at the end of the 12-month interventionl
|
Współpracownicy i badacze
Sponsor
Współpracownicy
Śledczy
- Krzesło do nauki: Hui Wang, Peking University Health Science Center
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Szacowany)
Zakończenie podstawowe (Szacowany)
Ukończenie studiów (Szacowany)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- IRB00001052-25212
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .