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Clinical Trials/NCT05889078
NCT05889078
Active, not recruiting
Not Applicable

The Effects of Walking in Nature (vs. an Urban Setting) on the Wellbeing of Postsecondary Students.

McGill University1 site in 1 country80 target enrollmentNovember 9, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Affect
Sponsor
McGill University
Enrollment
80
Locations
1
Primary Endpoint
Change in baseline negative affect at 4 weeks
Status
Active, not recruiting
Last Updated
2 years ago

Overview

Brief Summary

The goal of this randomized controlled trial is to examine the effects of a walking intervention (3 walks per week for a period of 4 weeks) in a nature vs. urban setting on the wellbeing of young adult postsecondary students. We will examine changes in positive and negative affect for participants assigned to the nature condition vs those assigned to the urban condition (primary outcome). We will also examine changes in reported depression and anxiety symptoms, perceived stress levels, sleep quality, mindfulness and wellbeing (secondary outcome).

Registry
clinicaltrials.gov
Start Date
November 9, 2022
End Date
May 30, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Marie-Claude Geoffroy

Dr Marie-Claude Geoffroy, assistant professor

McGill University

Eligibility Criteria

Inclusion Criteria

  • aged 18-25 years
  • speaks English
  • had working smartphone that can track walk routes using a smartphone application

Exclusion Criteria

  • inability to walk for 45 minutes due to serious medical reasons (eg surgery)
  • heart condition

Outcomes

Primary Outcomes

Change in baseline negative affect at 4 weeks

Time Frame: 4 weeks (1x per week for 4 weeks)

Measured by the Positive and Negative Affect Schedule. Total scores range from 10-50 for negative affect, with higher scores indicating higher levels of negative affect (a worse outcome).

Change in baseline positive affect at 4 weeks

Time Frame: 4 weeks (1x per week for 4 weeks)

Measured by the Positive and Negative Affect Schedule. Total scores range from 10-50 for positive affect, with higher scores indicating higher levels of positive affect (a better outcome).

Secondary Outcomes

  • Change in baseline mindfulness at 5 weeks(5 weeks (1 week following completion of study intervention))
  • Change in baseline anxiety symptoms at 5 weeks(5 weeks (1 week following completion of study intervention))
  • Change in baseline perceived stress levels at 5 weeks(5 weeks (1 week following completion of study intervention))
  • Change in baseline levels of wellbeing at 5 weeks(5 weeks (1 week following completion of study intervention))
  • Change in baseline depression symptoms at 5 weeks(5 weeks (1 week following completion of study intervention))
  • Change in baseline sleep quality at 5 weeks(5 weeks (1 week following completion of study intervention))
  • Change in baseline non-suicidal self-injury at 5 weeks(5 weeks (1 week following completion of study intervention))

Study Sites (1)

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