- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06928311
This Study Explores Whether Adding Natural Elements Like Plants and Sunlight to Indoor Gyms Makes Exercise Feel Easier, More Enjoyable, and Improves Performance. By Comparing Workouts in Nature-inspired and Plain Gym Settings, it Aims to Find Better Ways to Design Fitness Spaces in Cities.
Examining the Influence of Biophilic Design on College Students' Exercise Performance: A Crossover Study
The goal of this observational study is to examine whether exercising in a biophilic environment - a space designed to include natural elements like real plants, simulated sunlight, nature sounds, and outdoor views - can improve exercise performance and enjoyment compared to a standard indoor gym environment in male college students age 18-25 who have regularly exercised prior.
The main question it aims to answer is: "Can biophilic design enhance the physical and mental benefits of indoor exercise?"
Researchers will compare the two environments to see if there is any changes in exercise performance and enjoyment for each participant.
Participants will complete a treadmill fitness test in both settings to compare physical outcomes like maximal aerobic capacity, so the maximal amount of oxygen one can use during exercise, as well as perceived effort. After each treadmill test participants will be given surveys where they will be asked to evaluate their mood and enjoyment in that environment.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Colorado
-
Fort Collins, Colorado, United States, 80521
- Colorado State University Cardio Room (Moby Arena 134)
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Men between 18 and 25 years
Exclusion Criteria:
- Resting BP greater than 140/90
- Resting HR greater than 100 bpm
- BMI greater than 30 kg/m^2
- inability to exercise at moderate to vigorous intensities
- major illness/health complication in the past
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Biophilic Design
The exercise environment will be designed with nature elements, real and artificial plants, a landscape wall paper, simulated sunlight, and nature sounds.
|
This intervention focused around the environmental design of the exercise room.
|
|
Experimental: Traditional Exercise Environment
The exercise environment will be designed like a traditional indoor gym setting.
With a treadmill at the center and no other purposeful design elements.
|
This intervention focused around the environmental design of the exercise room.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Maximal Aerobic Capacity (VO2Max)
Time Frame: Testing Day 1
|
This will be taken using a K5 metabolic cart measuring breath by breath
|
Testing Day 1
|
|
Maximal Aerobic Capacity (VO2Max)
Time Frame: Testing Day 2
|
This will be taken using a K5 metabolic cart measuring breath by breath
|
Testing Day 2
|
|
Rate of Perceived Exertion
Time Frame: Every minute during testing day 1
|
Participants will rate their perceived exertion every minute during the test and recovery period on a 6-20 scale.
|
Every minute during testing day 1
|
|
Rate of Perceived Exertion
Time Frame: Every minute during testing day 2
|
Participants will rate their perceived exertion every minute during the test and recovery period on a 6-20 scale.
|
Every minute during testing day 2
|
|
Mood and Enjoyment Survey
Time Frame: Post Test Day 1
|
Participants will receive a paper survey on mood and enjoyment to complete.
|
Post Test Day 1
|
|
Mood and Enjoyment Survey
Time Frame: Post Test Day 2
|
Participants will receive a paper survey on mood and enjoyment to complete.
|
Post Test Day 2
|
|
VO2 Plateau Duration
Time Frame: Post Test Day 1
|
The time at which the participant is exercising at near maximal capacity.
|
Post Test Day 1
|
|
VO2 Plateau Duration
Time Frame: Post Test Day 2
|
The time at which the participant is exercising at near maximal capacity.
|
Post Test Day 2
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Heart Rate
Time Frame: During Testing Day 1 and 2
|
Taken using a Garmin HR chest strap.
|
During Testing Day 1 and 2
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Kaigang Li, Colorado State University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 6530
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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