The Emotional, Physical and Cognitive Benefits of Purposeful Green Space Activities on Seniors

October 9, 2024 updated by: Jennifer Roe, University of Virginia
This project explores if various nature based activities can lead to acute improvements in emotional, physical and cognitive health outcomes and encouraging senior center (JABA) service users to return to a safe environment. The activities the investigators will use include walking in nature, engaging in physical planting and cerebral, citizen science based activities.

Study Overview

Detailed Description

This study builds on the previous experimental work and expands it to focus on older adults in the Charlottesville area. The study objective is to understand the impact of different types of activities in green settings on physical and mental health outcomes in older adults at JABA centers using a repeated measures, crossover design in 20 participants.

There are three activity sessions in this project; walking (contemplative), planting (physical) and citizen science (cerebral). The walking condition will be a short green walk (10-15 minutes). The planting session will be run by JABA staff and a Master Gardener and will allow participants an opportunity to be outdoors and plant and tend to plants. The citizen science session will be run by JABA staff and a consultant and will rely less on physical exertion but rather focus on understanding green space at a more academic level. All sessions will be outdoors and will follow COVID-19 guidelines in place at the time of testing.

Outcome Measures The investigators will use various measures to assess the impact of green activity on emotional, physical and cognitive health outcomes, including;

  • Loneliness; measured by the UCLA Loneliness Scale, a 3-item scale that captures feelings of loneliness.
  • Belonging; measured by the General Belonging Scale (GBS), a 12-item scale capturing social acceptance/inclusion and social rejection/exclusion.
  • Acute Mood; pre and post measures of mood will be taken using the UWIST Mood Adjective Checklist (MACL), an acute measure of hedonic tone, stress and arousal.
  • Restoration; Psychological restorative qualities of the setting measured by the Perceived Restorativeness Scale, a three point scale determining the restorative quality of activity spaces.
  • Physical Activity_OMNIT; In addition to the arousal measure of the MACL, the investigators used the 11 point scale (from 0 to 10) of the OMNIT Perceived Exertion scale (tiredness), to understand how physically tired the activities made them.
  • Physical Activity_OMNIH; In addition to the arousal measure of the MACL, the investigators used the 11 point scale (from 0 to 10) of the OMNIH Perceived Exertion scale (exertion), to understand how much perceived physical effort participants put in.
  • Accelerometer; the investigators will use accelerometers to measure participant movement throughout the activities to correlate with physical activity measures.

All outcome measures will be scored and subsequently analysed using a one-way ANOVA to determine if experimental condition leads to any statistically significant difference between outcome scores. The investigators will look for correlations between outcome measures in order to establish relationships between variables.

The investigators will also send a short survey to a number of JABA service users (n=30) to understand mood, wellbeing and current barriers to returning to their local JABA center. This survey will include the UCLA Loneliness Scale, the GBS, mood and physical activity measures included above, as well as broader questions assessing their experience of the lockdown and their needs for safe return to the center.

Participants will be sent consent information in advance and have an opportunity to talk to the research time prior to attending their first session. For all conditions, participants would meet at a pre-determined location near their local JABA center and taken to the activity site directly. Participants will complete the short surveys, listed above, both pre and post their activity. All activities will last around 20 minutes. Participants will return for two consecutive weeks to undertake the alternative activities to which they originally completed.

Activities Participants will undertake three activities, on separate days, throughout this project.

  1. Walking; this contemplative activity will see users taken to a local green space area near their center and encouraged to walk around the space. It is anticipated that walks will last around 15-20 minutes.
  2. Planting; this physical activity will see users, lead by a local Master Gardener, engage with planting vegetables/fruit in raised beds. Not only will this allow users a chance to engage physically with nature, but it is anticipated that the grown produce will be used for center users.
  3. Citizen Science; this cerebral activity sees users engage with local green spaces, under the instruction of a citizen scientist, to learn about the intricacies of the space. This may include lichen counts (or similar) where the main outcome is learning based.

Study Type

Interventional

Enrollment (Actual)

24

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Virginia
      • Charlottesville, Virginia, United States, 22903
        • University of Virginia

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

65 years and older (Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Over 65 years
  • A JABA center user
  • Can walk unassisted for 20 minutes
  • Willing to comply with COVID-19 regulations

Exclusion Criteria:

  • Under 65 years
  • Never used a JABA center
  • unable to walk unassisted for 20 minutes.
  • Unwilling to comply with COVID-19 regulations

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Non-Randomized
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Walking
This contemplative activity will see users taken to a local green space area near their center and encouraged to walk around the space. It is anticipated walks will last around 15-20 minutes.
Green space in which activities take place
Experimental: Citizen Science
This cerebral activity sees users engage with local green spaces, under the instruction of a citizen scientist, to learn about the intricacies of the space. This may include lichen counts (or similar) where the main outcome is learning based.
Green space in which activities take place
Experimental: Planting
This physical activity will see users, lead by a local Master Gardener, engage with planting vegetables/fruit in raised beds. Not only will this allow users a chance to engage physically with nature, but it is anticipated that the grown produce will be used for center users.
Green space in which activities take place

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Loneliness (Time 1)
Time Frame: Pre activity
Loneliness was measured by the University of California, Los Angeles (UCLA) Loneliness Scale, a 3-item scale that captures feelings of loneliness. Scores range from 3 to 9 with higher scores indicating higher levels of perceived loneliness
Pre activity
Loneliness (Time 2)
Time Frame: Post activity (20 minutes after pre-activity measure)
Loneliness was measured by the University of California, Los Angeles (UCLA) Loneliness Scale, a 3-item scale that captures feelings of loneliness. Scores range from 3 to 9 with higher scores indicating higher levels of perceived loneliness
Post activity (20 minutes after pre-activity measure)
Social Isolation (Time 1)
Time Frame: Pre activity
Social Isolation was measured by the General Belonging Scale (GBS), a 12-item scale capturing social acceptance/inclusion and social rejection/exclusion. Scores will range from 12 to 84, with higher scores indicating higher levels of perceived belonging.
Pre activity
Social Isolation (Time 2)
Time Frame: Post activity (20 minutes after pre-activity measure)
Social Isolation was measured by the General Belonging Scale (GBS), a 12-item scale capturing social acceptance/inclusion and social rejection/exclusion. Scores will range from 12 to 84, with higher scores indicating higher levels of perceived belonging.
Post activity (20 minutes after pre-activity measure)
Mood_hedonic Tone (Time 1)
Time Frame: Pre activity
Pre measures of mood (hedonic tone) was taken using the University of Wales Institute of Science and Technology (UWIST) Mood Adjective Checklist (MACL), an average measure of hedonic tone. The subscale will range from 4 to 16, with higher scores indicating higher valence.
Pre activity
Mood_hedonic Tone (Time 2)
Time Frame: Post activity (20 minutes after pre-activity measure)
Post measures of (hedonic tone) was taken using the University of Wales Institute of Science and Technology (UWIST) Mood Adjective Checklist (MACL), an average measure of hedonic tone. The subscale will range from 4 to 16, with higher scores indicating higher valence.
Post activity (20 minutes after pre-activity measure)
Well Aging_ Using Perceived Restorativeness Scale
Time Frame: Post activity (20 minutes after pre-activity measure). This measure is a post-condition measure only that measures restoration as a result of the condition. This cannot be done before exposure to the condition.
Psychological restorative qualities of the setting was measured by the Perceived Restorativeness Scale, a three point scale determining the restorative quality of activity spaces. Scores range from 4 to 28, with higher scores indicating higher levels of perceived restoration.
Post activity (20 minutes after pre-activity measure). This measure is a post-condition measure only that measures restoration as a result of the condition. This cannot be done before exposure to the condition.
Physical Activity_OMNIT
Time Frame: Post activity (20 minutes after pre-activity measure). OMNIT is administered post-activity ONLY.
In addition to the arousal measure of the MACL, the investigators used the 11 point scale (from 0 to 10) of the OMNIT Perceived Exertion scale (tiredness), to understand how physically tired the activities made them. Lower scores indicate the tasks are easy; higher scores indicate the tasks are hard.
Post activity (20 minutes after pre-activity measure). OMNIT is administered post-activity ONLY.
Physical Activity_OMNIH
Time Frame: Post activity (20 minutes after pre-activity measure). OMNIH is administered post-activity ONLY.
In addition to the arousal measure of the MACL, the investigators used the 11 point scale (from 0 to 10) of the OMNIH Perceived Exertion scale (exertion), to understand how much perceived physical effort participants put in. Lower scores indicate the tasks are easy; higher scores indicate the tasks are hard.
Post activity (20 minutes after pre-activity measure). OMNIH is administered post-activity ONLY.
Mood_Stress (Time 1)
Time Frame: Pre activity
Pre measures of mood (stress) was taken using the University of Wales Institute of Science and Technology (UWIST) Mood Adjective Checklist (MACL), an average measure of stress. The subscale will range from 4 to 16, with higher scores indicating higher stress.
Pre activity
Mood_Stress (Time 2)
Time Frame: Post activity (20 minutes after pre-activity measure)
Post measures of mood (stress) was taken using the University of Wales Institute of Science and Technology (UWIST) Mood Adjective Checklist (MACL), an average measure of stress. The subscale will range from 4 to 16, with higher scores indicating higher stress.
Post activity (20 minutes after pre-activity measure)
Mood_arousal (Time 1)
Time Frame: Pre activity
Pre measures of mood (arousal) was taken using the University of Wales Institute of Science and Technology (UWIST) Mood Adjective Checklist (MACL), an average measure of arousal. The subscale will range from 4 to 16, with higher scores indicating higher arousal.
Pre activity
Mood_arousal (Time 2)
Time Frame: Post activity (20 minutes after pre-activity measure)
Post measures of mood (arousal) was taken using the University of Wales Institute of Science and Technology (UWIST) Mood Adjective Checklist (MACL), an average measure of arousal. The subscale will range from 4 to 16, with higher scores indicating higher arousal.
Post activity (20 minutes after pre-activity measure)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mobility Limitation
Time Frame: Throughout activity (measure taken for 20 minutes)
Mobility Limitation was determined using accelerometers to measure participant movement throughout the activities to correlate with physical activity measures.
Throughout activity (measure taken for 20 minutes)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Jenny Roe, University of Virginia

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 17, 2021

Primary Completion (Actual)

November 17, 2022

Study Completion (Actual)

November 17, 2022

Study Registration Dates

First Submitted

May 10, 2021

First Submitted That Met QC Criteria

May 31, 2021

First Posted (Actual)

June 4, 2021

Study Record Updates

Last Update Posted (Actual)

October 10, 2024

Last Update Submitted That Met QC Criteria

October 9, 2024

Last Verified

October 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • HSR210100
  • UL1TR003015 (U.S. NIH Grant/Contract)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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