Nature IDEAS Study: An RCT to Increase Time Spent in Nature Among University Students
Nature Dose Equity for Students
1 other identifier
interventional
1,545
1 country
9
Brief Summary
This project will first examine nature opportunities, belonging and benefits with a multi-state nature-based intervention with a focus on students of color. In light of the syndemic, 'nature deficit disorder' and poor mental health, the investigators anticipate several far-reaching impacts that will (a) test a nationally useful standardized way to quantify exposure; (b) invest in nature resources and accessibility on campuses; and (c) promote the mental health and therapeutic benefits of nature among young adults. These will lead to understanding the nature exposure and mental health interplay and techniques for quantifying and encouraging nature exposure to treat the on-going youth mental health crisis. Including HBCUs and an hispanic-serving institution is expected to result in heightened visibility of underlying disparities, including structural racism and land-based violence and discrimination, that have contributed to current-day nature gaps and dismantled nature relationships for students of color.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Sep 2024
Shorter than P25 for not_applicable
9 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 9, 2024
CompletedFirst Submitted
Initial submission to the registry
October 7, 2024
CompletedFirst Posted
Study publicly available on registry
October 9, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2025
CompletedSeptember 12, 2025
September 1, 2025
6 months
October 7, 2024
September 5, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Kessler-6
Kessler-6 changed to be a two week recall period. Range: 0-24. Higher scores indicate higher distress.
From enrollment to end of participation phase, 4 weeks.
Worry
Single question "I worry all the time" on a likert-type scale. Source: https://pubmed.ncbi.nlm.nih.gov/29214862/. Values range from 1-5, whereby a higher score indicates more frequent worry.
from enrollment to the final survey (4 week period)
Positive and Negative Affect Scale
This scale is comprised of 20 items, with 10 items measuring positive affect (e.g., excited, inspired) and 10 items measuring negative affect (e.g., upset, afraid). Each item is rated on a five-point Likert Scale, ranging from 1 = Very Slightly or Not at all to 5 = Extremely, to measure the extent to which the affect has been experienced, over a two-week period. Positive affect range: 10-50, whereby higher values indicate higher positive affect. Negative affect range: 10-50, whereby higher values indicate higher negative affect.
from emrollment to the final survey (4 week period)
Secondary Outcomes (2)
NR-6
From enrollment to the final survey (4 week period)
Access to Nature scale
from enrollment to the final survey (4 week period)
Study Arms (2)
Control group receiving standard health information
NO INTERVENTIONThis group will receive information about health benefits in nature.
Intervention Group receiving standard health information + incentives to increase time outdoors
ACTIVE COMPARATORThis group will receive information on the health benefits of time outdoors, a request to increase their time outdoors, eligibility to receive a prize, and information on peer performance.
Interventions
This intervention includes requesting an increase in time spent outdoors, eligibility to receive a prize, and information on peer performance.
Eligibility Criteria
You may qualify if:
- Undergraduate student
- years of age
- Lives within 30 miles of university campus
You may not qualify if:
- Not an undergraduate student
- Under 18 or over 24 years of age
- Lives \> 30 miles from the university campus
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Michigan State Universitylead
- Cleveland State Universitycollaborator
- Clemson Universitycollaborator
- University of Virginiacollaborator
- University of Marylandcollaborator
- University of Maryland Eastern Shorecollaborator
- Morgan State Universitycollaborator
- University of New Mexicocollaborator
- North Carolina Agricultural and Technical Universitycollaborator
- REI Cooperative Action Fundcollaborator
- Medical College of Wisconsincollaborator
Study Sites (9)
Morgan State University
Baltimore, Maryland, 21251, United States
University of Maryland
College Park, Maryland, 20742, United States
University of Maryland Eastern Shore
Salisbury, Maryland, 21804, United States
Michigan State University
East Lansing, Michigan, 48824, United States
University of New Mexico
Albequerque, New Mexico, 87131, United States
North Carolina A&T University
Greensboro, North Carolina, 27411, United States
Cleveland State University
Cleveland, Ohio, 44115, United States
Clemson University
Clemson, South Carolina, 29631, United States
University of Virginia
Charlottesville, Virginia, 22902, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
October 7, 2024
First Posted
October 9, 2024
Study Start
September 9, 2024
Primary Completion
March 1, 2025
Study Completion
March 1, 2025
Last Updated
September 12, 2025
Record last verified: 2025-09
Data Sharing
- IPD Sharing
- Will not share