- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT03665857
Childhood Obesity Intervention Study
A School-based Multicomponent Intervention Study for Preventing Excessive Weight Gain Among Primary School Students
Globally, childhood overweight and obesity is a public health problem. Although the rising trend in children's body mass index (BMI) has plateaued in some high-income countries, it has accelerated in low- and middle-income countries. It is especially true amongst Chinese children with the annual increase rate of obesity during 2010-2014 greater than any other periods from 1985 to 2010.
With the dramatic economic development in China, children are now growing up in an increasingly 'obesogenic' environment. For example, the availability and ubiquity of computers and smart phones promote sedentary time, and access to energy dense food and sugar sweetened beverages is now widespread. Effective childhood obesity intervention is urgently needed in China. Although over 20 intervention studies for overweight/obesity among children and adolescents have been conducted in China since the 1990s, most of them had moderate or serious methodological weaknesses. For example, they did not report the number of students, schools or districts initially approached to participate, raising the possibility of selection and recruitment bias. Additionally, although they stated the allocation of intervention and control were randomized, no description of the method of randomization was reported.
Given the relative lack of high-quality interventions for childhood overweight/obesity, the investigators designed a cluster randomized controlled trial to assess the effectiveness of a multicomponent one-academic-year intervention among 24 primary schools (approximately 1200 students) in the eastern (Beijing), middle (Shanxi) and western (Xinjiang) part of China.
The study aims to identify: 1) whether the school-based intervention will be effective for preventing excessive weight gain among children; 2) whether the intervention will be beneficial for improving healthy eating, physical activity and reducing sedentary behaviors among children.
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Studietype
Registrering (Faktiske)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiesteder
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Beijing, Kina
- Department of Maternal and Child Health, School of Public Health, Peking University
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
1. Eligibility criteria for schools The trial recruited a total of 24 schools. A convenience sample of 8 schools were selected from Beijing, Shanxi (Changzhi City) and Xinjiang (Urumqi City) respectively.
Inclusion Criteria for schools:
- school leader agreeing to implement this intervention; requiring school teachers who can implement this intervention (e.g. school doctors, physical education teachers, physical education teachers, etc.); having at least 50 children from Grade 4 (at the start of the intervention) per school;having a even number of schools within each district.
Exclusion Criteria for schools:
boarding schools;schools solely for children with special skills; schools of minor ethnic groups; similar programme (focus on weight gain prevention) would be conducted in schools during the study period; schools having a cancelling or relocation plan during the study period.
2. Eligibility criteria for classes One class per school will be selected if the estimated number of students enrolled in the programme is no less than 40 within the selected class; two classes per school will be selected if the estimated number of students enrolled in the programme is less than 40 within the selected class.
3. Eligibility criteria for students Eligible children will be those whose primary caregivers will provide written consent to participate the study. After collecting students' medical history from their parents, we will exclude individuals suffering from or having a history of any cardiovascular and metabolic diseases, asthma and disabilities that limit their ability to perform physical activity.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Forebygging
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Enkelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
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Eksperimentell: multicomponent intervention
Schools in the intervention arm will receive a multicomponent intervention at the school-, parent- and student-level, with a mobile application to promote the collaboration between investigators, school teachers, parents and students. The school-level intervention elements will include school policies and health education for teachers. The parent-level intervention elements will include health education for parents and promoting students' physical activity at home. The student-level intervention elements will include health education for students, promoting students' physical activity in school and monthly monitoring of weight and height. |
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Ingen inngripen: usual-care control
Schools assigned to the control group will have usual education provision throughout their participation in the trial, and after finishing the study they will be offered the health education package, policy suggestion and materials as the schools in the multicomponent intervention group.
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
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Students' BMI change immediately after the intervention completion
Tidsramme: at end of the 8-month intervention
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the difference between arms in the change of students' BMI immediately after the intervention completion
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at end of the 8-month intervention
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Students' BMI change one year after the intervention completion
Tidsramme: at 15 months following the end of the intervention
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the difference between arms in the change of students' BMI one year after the intervention completion
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at 15 months following the end of the intervention
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Students' BMI-Z change
Tidsramme: 1. at end of the 8-month intervention; 2. at 15 months following the end of the intervention
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use BMI to calculate BMI-Z score based on WHO growth chart
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1. at end of the 8-month intervention; 2. at 15 months following the end of the intervention
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The change of prevalence of childhood overweight/obesity
Tidsramme: 1. at end of the 8-month intervention; 2. at 15 months following the end of the intervention
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define childhood overweight or obesity based on international BMI percentile criteria (IOTF)
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1. at end of the 8-month intervention; 2. at 15 months following the end of the intervention
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The change of incidence of childhood overweight/obesity
Tidsramme: 1. at end of the 8-month intervention; 2. at 15 months following the end of the intervention
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define childhood overweight or obesity based on international BMI percentile criteria (IOTF)
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1. at end of the 8-month intervention; 2. at 15 months following the end of the intervention
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The change of students' waist circumference
Tidsramme: 1. at end of the 8-month intervention; 2. at 15 months following the end of the intervention
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measure waist circumference
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1. at end of the 8-month intervention; 2. at 15 months following the end of the intervention
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The change of students' waist-to-hip circumference ratio
Tidsramme: 1. at end of the 8-month intervention; 2. at 15 months following the end of the intervention
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measure waist circumference and hip circumference to calculate waist-to-hip circumference ratio
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1. at end of the 8-month intervention; 2. at 15 months following the end of the intervention
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The change of both systolic and diastolic blood pressures among students
Tidsramme: 1. at end of the 8-month intervention; 2. at 15 months following the end of the intervention
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measure systolic and diastolic blood pressure by using electronic sphygmomanometer
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1. at end of the 8-month intervention; 2. at 15 months following the end of the intervention
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The change of body fat percentage among students
Tidsramme: at end of the 8-month intervention
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measure body fat percentage by bioelectrical impedance analysis
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at end of the 8-month intervention
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The change of one-minute rope skipping test outcomes among students
Tidsramme: at end of the 8-month intervention
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count the number of one-minute rope skipping
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at end of the 8-month intervention
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The change of one-minute sit-up test outcomes among students
Tidsramme: at end of the 8-month intervention
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count the number of one-minute sit-up test
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at end of the 8-month intervention
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The change of endurance run (50 metre*8) test outcomes among students
Tidsramme: at end of the 8-month intervention
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record the time of endurance run (50 metre*8)
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at end of the 8-month intervention
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The change of standing long jump test outcomes among students
Tidsramme: at end of the 8-month intervention
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measure the distance of standing long jump
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at end of the 8-month intervention
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The change of students' knowledge related to energy balance
Tidsramme: at end of the 8-month intervention
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We will use a self-designed questionnaire including 8 items to assess the change of students' knowledge related to energy balance.
For example, we will ask students, "Is it right that drinking sugar-sweetened beverage cannot substitute drinking water."
Three choices will be provided (Right; Wrong; Not clear).
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at end of the 8-month intervention
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The change of students'duration of moderate-to-vigorous physical activity
Tidsramme: at end of the 8-month intervention
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Questions were designed based on a validated 7-day physical activity questionnaire.
Kappa values for a two-week test-retest ranged from 0.46 to 0.79.
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at end of the 8-month intervention
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The change of students' eating behavior
Tidsramme: at end of the 8-month intervention
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We will use a parent-rated "Children Eating Behavior Questionnaire" (CEBQ) to assess students' eating behaviors, including responsiveness to food, enjoyment of food etc.
This 35-item instrument has been shown relatively good reliability.
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at end of the 8-month intervention
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The change of students' sedentary behavior
Tidsramme: at end of the 8-month intervention
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We will use a self-designed questionnaire to ask the average duration of doing homework, watching television and playing electronic devices per day during the last week, respectively.
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at end of the 8-month intervention
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The change of school-level policies for childhood overweight/obesity
Tidsramme: at end of the 8-month intervention
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We will use a self-designed questionnaire to measure school obesity-related policies involving school administration, health education, management of overweight or obesity, communication with the families of students and school lunch.
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at end of the 8-month intervention
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Andre resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
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The stage of change related to weight reduction behavior
Tidsramme: at end of the 8-month intervention
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We will use two items to assess it.
First, we will ask "Have you taken action to reduce your weight during the last three months?"
Yes/no choices will be provided.
And then, we will ask "Do you intend to reduce your weight currently?"
This item will be provided 5 choices from "completely not intend" to "intend very much".
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at end of the 8-month intervention
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Samarbeidspartnere og etterforskere
Sponsor
Etterforskere
- Hovedetterforsker: Hai-Jun Wang, PhD, Peking University
Publikasjoner og nyttige lenker
Generelle publikasjoner
- Liu Z, Gao P, Gao AY, Lin Y, Feng XX, Zhang F, Xu LQ, Niu WY, Fang H, Zhou S, Li WH, Yuan JH, Xu CX, Wu N, Li HJ, Wen LM, Patton GC, Wang HJ, Wu YF. Effectiveness of a Multifaceted Intervention for Prevention of Obesity in Primary School Children in China: A Cluster Randomized Clinical Trial. JAMA Pediatr. 2022 Jan 1;176(1):e214375. doi: 10.1001/jamapediatrics.2021.4375. Epub 2022 Jan 4.
- Liu Z, Wu Y, Niu WY, Feng X, Lin Y, Gao A, Zhang F, Fang H, Gao P, Li HJ, Wang H; study team for the DECIDE-children study. A school-based, multi-faceted health promotion programme to prevent obesity among children: protocol of a cluster-randomised controlled trial (the DECIDE-Children study). BMJ Open. 2019 Nov 2;9(11):e027902. doi: 10.1136/bmjopen-2018-027902.
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 2016YFC1300204
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
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