Denne side blev automatisk oversat, og nøjagtigheden af ​​oversættelsen er ikke garanteret. Der henvises til engelsk version for en kildetekst.

Study on the Tailored Intervention Strategy of Childhood Obesity Based on Monitoring Physical Activities and Dietary Behaviors

27. august 2014 opdateret af: Wang Jingjing
The project aims at developing the tailored intervention strategy of childhood obesity based on monitoring physical activities with accelerometer and dietary behaviors using diary. It probably raise the passion of obese children to control weight, form healthy life style, be effective in sustaining weight loss and early prevent adulthood diseases.

Studieoversigt

Detaljeret beskrivelse

The overweight and obese primary school students from 1-5 grades will be recruited according to "Body Mass Index Reference for Screening Overweight and Obesity in Chinese School-age Children". The participants with will be allocated with schools as the unit to four groups: tailored intervention based on monitoring physical activity and dietary behaviors, exercise intervention group based on the Happy 10 program, nutrition education intervention group. The three intervention groups received the designed interventions for the duration of 1 year. Before and after the intervention, we will carry out a questionnaire survey, a physical measurement, a fitness test, and a metabolic markers detection

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

450

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

      • Beijing, Kina, 100191
        • Insitute of Child and Adolescent Health, Peking University

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

7 år til 12 år (Barn)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Overweight and obese children from grade 1-5 primary schools

Exclusion Criteria:

  • Students with any contraindication or physical diseases (heart, Lung, liver, kidney, other vital organs, endocrine diseases and drug side effects et al.) and psychological illnesses that may prevent them from participating in physical activity and eating a normal diet were excluded

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Forebyggelse
  • Tildeling: Ikke-randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Dobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Tailored intervention group

For the monitoring session, physical activity was assessed by accelerometer and dietary was assessed by diary. Based on the monitoring information, the individual tailored prescription, including the normative feedback and process feedback, were formed and delivered to children and parents. Children were encouraged to modify the behaviors according to the prescription.

Then, next monitoring circle was followed. In total, 7 monitoring round were completed.

Andre navne:
  • ZhiJi accelerometer UX-02 as physical activity monitor
Eksperimentel: Happy 10 exercise group
All the schools participating in this group were encouraged to take two Happy 10 sessions on each school day.
Andre navne:
  • happy 10 program developed by Center for Disease Control and Prevention, China
Eksperimentel: Nutrition education group
The nutrition intervention was mainly conducted based on the nutrition knowledge through health education lectures given by researchers. The lectures were given for eight times to students and twice to parents. Each lecture session lasted no less than 40 min.
Ingen indgriben: Control group
Receive no intervention

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
Change in body mass index
Tidsramme: Baseline, 1-year post-intervention
Baseline, 1-year post-intervention

Sekundære resultatmål

Resultatmål
Tidsramme
Change in obesity-related anthropometric measurements
Tidsramme: Baseline, 1-year post-intervention
Baseline, 1-year post-intervention
Change of blood pressure
Tidsramme: Baseline, 1-year post-intervention
Baseline, 1-year post-intervention
Change of biomarkers for disease risk
Tidsramme: Baseline, 1-year post-intervention
Baseline, 1-year post-intervention
Change of attitude, knowledge, and behaviors on dietary and physical activity
Tidsramme: Baseline, 1-year post-intervention
Baseline, 1-year post-intervention

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. maj 2009

Primær færdiggørelse (Faktiske)

1. december 2011

Datoer for studieregistrering

Først indsendt

27. august 2014

Først indsendt, der opfyldte QC-kriterier

27. august 2014

Først opslået (Skøn)

29. august 2014

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

29. august 2014

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

27. august 2014

Sidst verificeret

1. august 2014

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • IRB00001052-10081

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Abonner