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An Evaluation of "Growing Healthy Places: Mississauga"

B

Brock University

Status

Active, not recruiting

Conditions

Obesity &Amp; Overweight
Physical Activity
Quality of Life (QOL)
Body Esteem
Diet Quality
Community

Treatments

Behavioral: Community Co-designed Physical Activity and Diet Intervention Package

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT07191925
REB24-273

Details and patient eligibility

About

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)

Enrollment

4,900 estimated patients

Sex

All

Ages

6 to 13 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

4,900 participants in 2 patient groups

Intervention Group
Experimental group
Description:
Receive a community co-designed package of multi-level, multi-component interventions targeting physical activity and diet
Treatment:
Behavioral: Community Co-designed Physical Activity and Diet Intervention Package
Control Group
No Intervention group
Description:
Usual school and community practices with no interventions from the study

Trial contacts and locations

1

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Central trial contact

Karen Patte, PhD; Katelyn Battista, PhD

Data sourced from clinicaltrials.gov

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