Experimental
Conditions
Keywords
Clinical depression, Stress, Group-walking, Walking condition (nature vs urban)
Brief summary
Over the past few years, a growing number of campaigns from around the world, including Canada, are highlighting the positive impact of spending time in nature on well-¬being. Indeed, mounting evidence suggests that spending time with nature is associated with a myriad of affective and cognitive benefits. Surprisingly few studies to date have tested the assumption that walking in nature versus in urban settings could alleviate stress and depressive symptoms in clinically depressed adults. The main purpose of this study is to investigate the effectiveness of walking in nature versus in urban settings to improve depression related symptoms and reduce stress. The trial initially included 2 primary outcomes: patients stress levels (salivary cortisol) and depression-related symptoms (eg, affect, rumination, executive functioning). However, due to hygienic concerns in light of the COVID-19 pandemic in 2020, the collection of saliva samples (and in turn, the measurement of stress levels via salivary cortisol) was removed from the study's procedure. The main outcome was changed to effects on positive and negative affect.
Interventions
BEHAVIORALWalking in Urban setting
Walking for 60 minutes as described above
BEHAVIORALWalking in nature setting
Walking for 60 minutes as described above
Sponsors
Social Sciences and Humanities Research Council of Canada
McGill University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)
Masking description
Participants were unaware as to whether they were assigned to an urban or nature walking condition
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
* Men and women aged between 18 and 65 years, inclusively; * Ability to speak French or English; * Diagnosis major depressive disorder (DSM-IV);
Exclusion criteria
* Acute psychotic symptoms; * Acute suicidal intent (within 48 hours); * Unable to walk for 60 min or serious medical reasons (e.g. major surgery) * Heart condition as per history or detected on electrocardiogram
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in affect from baseline up to 48 hours post-walk | Day 1 to Day 3 | Positive and Negative Affect Schedule (PANAS) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in Executive Functions | The Stroop test will be administered at 2 time points: 1) before the walk (between 9:45-10:30); 2) after the walk (between 11:30-11:50) | The stroop color word test is a widely used task to assess selective attention and inhibitory control. In the first block of this task (A), color words (red, blue, yellow, green) printed in black ink are presented in random order and participants are asked to read out loud the words. In the second block (B), solid color patches in one of the same four colors are shown and participants name the colors. Finally, in the third block (C), color words are printed in an incongruous ink color and participants must name the ink color (e.g. GREEN \[typed in red\]; response = red). Participants are asked to complete each block as quickly and accurately as possible and the time to complete each trial is calculated and averaged for each block. An interference score is calculated as followed: C - \[(A + B) /2\]. |
| Change in suicidal Ideations | Day 1 | Severity of Suicidal Ideations The severity of current suicidal ideation will be assessed with three items derived from a prior study of momentary assessment of suicidal risk: How intense is your desire to kill yourself right now?; How strong is your intention to kill yourself right now?; How strong is your ability to resist the urge to kill yourself right now? Each item is scored on a scale from 0 (not strong \[intense\] at all) to 4 (very strong \[intense\]). |
| Change in depressive symptoms | Day 1 to Day 2 | The Beck Depression Inventory (BDI-II) The BDI is a widely used 21-item depression inventory with good internal consistency (α = .93 in the current sample) and validity. Items are answered on a 4-point scale from 0 to 3. |
| Change in rumination | Day 1 | The Rumination-Reflection Questionnaire (RRQ) The RRQ is a 24-item self-reported questionnaire assessing both self-rumination and self-reflection, 57 with 12 items corresponding to each subscale. Participants rate the degree to which they engage in self- rumination (e.g. sometimes it is hard for me to shut off thoughts about myself) and self-reflective thoughts (e.g. I love to meditate on the nature and meaning of things) on a Likert scale ranging from one (strongly disagree) to five (strongly agree) |
| Change in irritability | Day 1 to Day 3 | The Brief Irritability Test (BITe): The BITe is a 5-item self-report measure of irritability that is suitable for use among men and women. Participants respond to statements using a 6-point Likert scale ranging from Never to Always. Items include the following five statements: I have been grumpy; I have been feeling like I might snap; Other people have been getting on my nerves. |
Countries
Canada
Outcome results
None listed