- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT01626807
Evaluation of a Walking School Bus Program
Evaluation of a Walking School Bus Program: A Cluster Randomized Controlled Trial
Just two generations ago, walking or bicycling to school was the norm for a substantial number of US children, e.g. 48% of children walked or biked to school in 1969 versus only 13% in 2009. This decline occurred in the same timeframe as the childhood obesity epidemic, which is at record high levels in the US and affects low-income and ethnic minority children the most. This project will test "the walking school bus" (WSB) program, in which children walk to and from school with adults, and its impact on low-income, ethnic minority children's walking to school, physical activity, and risk for obesity. Ultimately, this line of research has the potential to provide a low-cost, easy to disseminate program to reduce risk of obesity and cancer for at-risk children.
The investigators Specific Aims among 3rd-5th grade children include:
SA1) To recruit 770 child-parent dyads from 22 elementary schools over 4 years and conduct a cluster randomized controlled trial to assess the efficacy of a WSB program on children's walking to school, physical activity, and BMI z-score over a school-year SA2) To collect and analyze data on individual-, school-, and macro-level influences on changes to children's walking to school resulting from the WSB program
The Primary Hypotheses to be tested, in comparison to control children, include:
H1) The WSB program will increase children's walking to school over a school-year.
H1a) Parents' outcome expectations and self-efficacy will mediate the relationship between the WSB and changes to children's walking to school.
H1b) Walkability, safety, and acculturation will moderate changes to children's walking to school.
H2) The WSB program will increase children's physical activity and decrease BMI z-scores over a school-year.
H3) The WSB program will increase school-level pedestrian safety behaviors over a school-year.
Studieöversikt
Status
Betingelser
Intervention / Behandling
Studietyp
Inskrivning (Faktisk)
Fas
- Inte tillämpbar
Kontakter och platser
Studieorter
-
-
Washington
-
Seattle, Washington, Förenta staterna, 98145-5005
- Seattle Children's Research Institute
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
Inclusion Criteria:
- physically capable of walking to and from school
- live within 1-mile of school or parents agree to regularly drop off children within 1-mile of school
- attend a study school and enrolled in 3rd, 4th, or 5th grade
Exclusion Criteria:
- another child from the same household is enrolled in the study
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Förebyggande
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Enda
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Inget ingripande: Vanlig skötsel
|
|
|
Experimentell: Walking school bus
|
Children will have the option of walking to and/or from school with study staff who are trained in Safe Routes to School methods.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Tidsram |
|---|---|
|
Weekly rate of children's active commuting to school
Tidsram: 5-6 months
|
5-6 months
|
Sekundära resultatmått
Resultatmått |
Tidsram |
|---|---|
|
Moderate-to-vigorous physical activity
Tidsram: 5-6 months
|
5-6 months
|
|
Body mass index z-score
Tidsram: 5-6 months
|
5-6 months
|
Samarbetspartners och utredare
Sponsor
Utredare
- Huvudutredare: Jason A Mendoza, MD, MPH, Seattle Children's Research Institute
Publikationer och användbara länkar
Användbara länkar
Studieavstämningsdatum
Studera stora datum
Studiestart
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Uppskatta)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- 1R01CA163146-01A1 (U.S.S. NIH-anslag/kontrakt)
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