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Recruiting NCT07147634

Outdoor Science Education and Child Well-being in Primary Schools: Protocol for a Cluster Randomized Controlled Trial on Learning, Connection to Nature, Eco-anxiety, and Stress

No phase Interventional Healthy Children

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Outdoor science education, Indoor classroom-based science education.
Who it may be relevant to
Registry conditions: Healthy Children. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Canada
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The goal of this randomized controlled trial is to learn if an outdoor science education intervention can improve primary school students' learning and well-being when compared to an indoor classroom-based science education intervention. The main questions it aims to answer are: * Will students who engage in outdoor science learning produce higher-quality observations of living organisms than students who receive instruction exclusively in an indoor, classroom-based context, when both groups are invited to make observations in an unfamiliar natural environment? * Does an outdoor education intervention embedded within the science curriculum contribute to children's connection to nature, eco-anxiety and stress? Participants will: * Receive a science education intervention 2h/week for a total of 5 weeks, either indoors or outdoors * Answer questionnaires before and after the intervention * Participate in a field day-trip after the intervention where they will be asked to observe living organisms.

Interventions

  • Behavioral Outdoor science education
    Following Québec's mandatory curriculum, primary school teachers will provide life science lessons 2h/week for a total of 5 weeks in an outdoor setting
  • Behavioral Indoor classroom-based science education
    Following Québec's mandatory curriculum, primary school teachers will provide life science lessons 2h/week for a total of 5 weeks inside the classroom

Primary outcome measures

  • Score on the Scientific Observation Skills Rubric (0-15) in a Novel Environmental Context [Time frame: After the 5-week intervention has ended, students will spend one day in a new environmental context (at the end of October) in order to make observations]
Secondary outcome measures (4)
  • Connection to nature - Score on the Inclusion of Nature in Self Scale (0-7) [Time frame: At baseline and immediately after the 5-week intervention has ended]
  • Score on the Perceived Stress Scale for Children (PSS-C; range 0-39) [Time frame: At baseline and immediately after the 5-week intervention has ended]
  • Score on the 11-item Hogg Eco-Anxiety Scale (HEAS-13; range 0-33) [Time frame: At baseline and immediately after the 5-week intervention has ended]
  • Score on the Basic Psychological Needs Satisfaction Scale - School Version (range 0-36) [Time frame: Baseline and immediately after the 5-week intervention]

Eligibility criteria

Inclusion criteria

  • Primary schools need to have a deprivation index equal to or superior to 1 (with 10 being the maximum) and be located in Montreal, Longueuil or Laval (QC).
  • Teachers have to show some interest in outdoor education but are not obliged to have already done some before in order to be included.
  • Only 5th and 6th grade teachers are included.
  • Primary schools with two teachers interested in participating in the project.

Exclusion criteria

  • Alternative schools or those welcoming recently arrived non-Francophone students are not included.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Other

Study locations

Canada · 1 center
  • Greater Montreal area (Laval, Longueuil, Montreal) — Montreal

Identifiers

NCT: NCT07147634 · 2023-3453 · 435-2022-0651

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗