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CompletedNCT05830656HybridNatureUpdated Jul 6, 2023

Hybrid- Nature: Recovering From Work Through Nature Experiences

An interventional study of Exposure to nearby nature and Exposure to virtual nature in Physiological Recovery, Psychological Recovery and Restorative Experiences, sponsored by JAMK University Of Applied Sciences. Completed at 1 site in Finland. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-07-06.

Sponsored by JAMK University Of Applied Sciences · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
57
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The research examines employees' recovery from work stress during visits in nearby nature and when viewing virtual nature with Virtual Reality (VR) goggles. The research provides information on the physiological and psychological recovery of employees who do remote or hybrid work. Recovery is analysed with qualitative and quantitative methods including Firstbeat Life measurements, surveys and interviews. The results can be used in workplaces to develop operating models to promote well-being in remote and hybrid work. The research generates new understanding on how employees' recovery can be supported by means of virtual nature tourism services.

Read the detailed description

An intervention study with a cross-over research design will be conducted among a sample of 60 employees who do remote or hybrid work. The intervention phase lasts in total of four weeks. During the first week (control phase), the participants continue their daily routine as normal. During the second week of the intervention, a half of the participants are randomised to visit a nearby natural area after finishing work (exposure to nearby nature). The other half of the participants are randomised to view virtual nature videos with VR goggles after finishing work (exposure to virtual nature). On the third week of the intervention, the participants complete nature exposure the other way around. That is, those participants who took part first in exposure to nearby nature will view virtual nature, and vice versa. On the fourth week of the intervention, the participants take part in a semi-structured focus group interview.

Recovering from work in nearby nature and virtual nature is examined through multidisciplinary perspectives of health, well-being, and tourism. The aim of the research is to find new ways of promoting work stress recovery, psychological detachment and restoration among employees when they are making the transition between work time and personal time. These research findings are particularly relevant for fields in which there has been a growing trend for remote or hybrid work. This research is funded by the Finnish Work Environment Fund (Project Number: 220076).

02

Conditions studied

  • Physiological Recovery
  • Psychological Recovery
  • Restorative Experiences

Keywords

  • Recovery
  • Nature
  • Employees
  • Work stress
  • Occupational well-being
  • Virtual Reality
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Employees who do remote or hybrid work
  • Able to communicate adequately in Finnish in order to participate

Exclusion criteria

Exclusion Criteria:

  • No exclusion criteria for study participation.
  • Firstbeat Life analyses are only available for participants who identify themselves on the basis of biological sex of female or male.
  • Firstbeat Life analyses might be unreliable for participants with some health-related issues (e.g., pacemaker, heart transplantation, complex cardiac disease, persistent atrial fibrillation or flutter, or uncontrolled thyroid disease) and therefore measurements will not be performed for them as a part of this research.
04

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
57 participants (actual)

Study arms

  • Experimental
    Control, Then exposure to nearby nature, Then exposure to virtual nature

    During the first week, the participants continue their normal routine at work and in leisure time. On the second week, the participants visit a nearby natural area after finishing their workday on three days (Tuesday, Wednesday, and Thursday). On the third week, the participants watch virtual nature videos with Virtual Reality (VR) goggles after finishing their workday on three days (Tuesday, Wednesday, and Thursday).

    Behavioral: Exposure to nearby nature · Behavioral: Exposure to virtual nature

  • Experimental
    Control, Then exposure to virtual nature, Then exposure to nearby nature

    During the first week, the participants continue their normal routine at work and in leisure time. On the second week, the participants watch virtual nature videos with Virtual Reality (VR) goggles after finishing their workday on three days (Tuesday, Wednesday, and Thursday). On the third week, the participants visit a nearby natural area after finishing their workday on three days (Tuesday, Wednesday, and Thursday).

    Behavioral: Exposure to nearby nature · Behavioral: Exposure to virtual nature

Interventions

  • BehavioralExposure to nearby nature

    Participants spend a minimum of 20 minutes in their favourite place in nearby nature.

  • BehavioralExposure to virtual nature

    Participants spend a minimum of 20 minutes watching virtual nature videos.

05

What researchers measure

Primary outcomes

  1. Psychological recovery

    Recovery Experience Questionnaire (REQ), the scores range from 1 to 5, a higher score refers to better psychological recovery.

    Time frame: Three weeks

Secondary outcomes

  1. Restorative experiences

    Restorative Outcome Scale (ROS), the scores range from 1 to 7, a higher score refers to better restoration.

    Time frame: Three weeks

  2. Work engagement

    Utrecht Work Engagement Scale (UWES), the scores range from 1 to 7, a higher score refers to higher work engagement.

    Time frame: Three weeks

  3. Burnout

    Burnout Assessment Tool (BAT), the scores range from 1 to 5, a higher score refers to higher burnout.

    Time frame: Three weeks

  4. Stress recovery

    A physiological measure of stress recovery balance, the scores range from 0 to 100, a higher score refers to better physiological stress recovery.

    Time frame: Three weeks

  5. Sleep quality

    A physiological measure of the restorative effect of sleep, the scores range from 0 to 100, a higher score refers to better recovery during sleep.

    Time frame: Three weeks

  6. Relax-Stress Intensity

    A physiological measure of the Relax-Stress Intensity (RSI), the scores range from -100 to 100, a higher score (+/- 100) refers to a stronger reaction.

    Time frame: Three weeks

  7. Body resources

    A physiological measure of body resources, the scores range from 0 to 100, a higher score refers to higher body resources.

    Time frame: Three weeks

06

Study locations

1 site
  • JAMK University of Applied Sciences
    Jyväskylä, 40100, Finland
07

References and documents

Individual participant data

Plan to share: Yes — Data from surveys and physiological measurements will be anonymised after the research and will be archived to the research data storage service (IDA). Anonymised data will open for reuse after the research finishes in 2024. The reuse of interview data will be restricted to suitable parts.

Supporting information: Study protocol

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT05830656
Lead sponsor
JAMK University Of Applied Sciences
Responsible party
Sponsor
First posted
Apr 26, 2023
Start date
Jan 17, 2023
Primary completion
Jun 8, 2023
Completion
Jun 16, 2023
Last update
Jul 6, 2023

Study contacts

Katriina Hyvönen, PhD
principal investigator · JAMK University Of Applied Sciences

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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