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.

December 9, 2025 updated by: Colorado State University

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

Study Type

Interventional

Enrollment (Actual)

25

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

    • Colorado
      • Fort Collins, Colorado, United States, 80521
        • Colorado State University Cardio Room (Moby Arena 134)

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

  • Adult

Accepts Healthy Volunteers

Yes

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

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: 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

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

Investigators

  • Principal Investigator: Kaigang Li, Colorado State University

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)

April 4, 2025

Primary Completion (Actual)

October 16, 2025

Study Completion (Actual)

November 1, 2025

Study Registration Dates

First Submitted

April 1, 2025

First Submitted That Met QC Criteria

April 7, 2025

First Posted (Actual)

April 15, 2025

Study Record Updates

Last Update Posted (Actual)

December 17, 2025

Last Update Submitted That Met QC Criteria

December 9, 2025

Last Verified

December 1, 2025

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)?

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.

Clinical Trials on Biophilic Environmental Design

Clinical Trials on Exercise Environment

Subscribe