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Clinical Trials in Canada / NCT07191925
Active, not recruiting Not applicable

An Evaluation of "Growing Healthy Places: Mississauga"

NCT07191925 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2025-10-16
Last updated
2025-11-21

Condition(s) studied

Quality of Life (QOL)Physical ActivityDiet QualityObesity &Amp; OverweightBody EsteemCommunity

Investigational drug(s) / intervention(s)

Community Co-designed Physical Activity and Diet Intervention Package

Community Co-designed Physical Activity and Diet Intervention Package: A package of 4-6 diet and physical activity interventions selected from a long-list of potential interventions and adapted to the unique school and neighborhood context via consultation with community stakeholders. Intervention packages are multi-level (i.e. targeting at least two of individual, external and structural environments), target elements of both diet and physical activity, and are health equity oriented in terms of both access and improvement. Long-list potential interventions include items related to school intramural programming, active transport, health education, community recreational programming, and structural/public space design improvements.

Study summary

The goal of this intervention study is to learn if community co-designed activities to improve diet and physical activity can impact the health of children ages 6-13 in Mississauga, Canada. The main questions it aims to answer are:

1. Do the community co-designed interventions improve health-related quality of life of children after one year and two years?
2. Do the community co-designed interventions improve the physical activity and eating behaviors of children after one year and two years?

Ten intervention and 12 control schools will take part in this study. The schools were recruited from the Mississauga area using an application process. Selection and group assignment involved a multi-stage process with initial randomization followed by manual adjustment (to balance groups on key observable characteristics and respond to stakeholder concerns about spillovers and implementation feasibility).

Researchers will compare students in schools that receive the interventions to students in schools that receive no interventions to see if the interventions improve health-related quality of life, increase physical activity and improve eating behaviors.

Participants will:

* attend participating elementary or middle schools (in either intervention neighborhoods or control neighborhoods)
* complete an anonymous questionnaire about their wellbeing, physical activity, and eating behaviors at baseline, after one year, and after two years
* potentially participate in school and community programs (if in an intervention school neighborhood)

Eligibility

Sex
ALL
Min age
6 Years
Max age
13 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Informed consent obtained by the child's parent or legal guardian before any study-related activities * Aged 6-13 years (both 6 and 13 allowed) at the time of signing consent * Enrolled in Grades 3-8 in one of the participating schools at the time of data collection Exclusion Criteria: * Parent(s) or legal guardians do not provide fully informed consent * Parent(s) or legal guardians withdraw their consent for their child participating in the research * Child does not agree to participate on the data collection day

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
School Board Mississauga Ontario

More Brock University trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07191925 on ClinicalTrials.gov ↗ ← All trials in Canada