- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05973461
Effects of Exercise and Virtual Reality on Depression
May 26, 2026 updated by: Xiangli Gu, PhD, The University of Texas at Arlington
Effects of Exercise With Virtual Reality on Females and Males With or Without Depression
This study is evaluating the effects of riding on a cycle ergometer while experiencing virtual reality to determine its effect on mood.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Adults (males and females) above the age of 18 yrs will be recruited to determine if they have symptoms of depression based on a questionnaire (Center for Epidemiologic Studies - Depression Scale (CES-D).
They will then complete a Beck Inventory before and after the exercise.
Participants will be divided into groups either having symptoms of depression or not.
They will be randomized to ride on a cycle ergometer with or without using Virtual Reality (VR) that will allow them to view neighborhoods or parks during the exercise.
The ergometer will be set at resistance raising the heart rate to 65% of their age-predicted heart rate maximum.
They will ride for 20 min and then complete the Beck Inventory to determine any changes in their depressive symptoms.
Study Type
Interventional
Enrollment (Estimated)
200
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 Contact
- Name: Judy R Wilson, Ph.D.
- Phone Number: 817-272-3128
- Email: jrwilson@exchange.uta.edu
Study Contact Backup
- Name: Xiangli Gu, Ph.D.
- Email: xiangli.gu@uta.edu
Study Locations
-
-
Texas
-
Arlington, Texas, United States, 76019
- Recruiting
- UTArlington
-
Contact:
- Judy R Wilson, Ph.D.
- Phone Number: 817-272-3128
- Email: jrwilson@exchange.uta.edu
-
Contact:
- Xiangli Gu, Ph.D.
- Email: xiangli.gu@uta.edu
-
-
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
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Males and females over the age of 18 years
- With or without symptoms of depression
- Physically inactive or sedentary (less than 30 minutes per day)
- Normal vision and no color blindness
- No physical disorders such as walking with assistance
Exclusion Criteria:
- Below the age of 18 years or over 65 years,
- Women who are pregnant
- Individuals who have been diagnosed with mental disorders
- Individuals with leg injuries
- Individuals with cardiac problems
- Individuals with a history of asthma
- Individuals with a body mass index over 30.
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: Screening
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Cycle Ergometer and Virtual Reality
30 min ride on cycle ergometer while viewing neighborhood scenes using virtual reality
|
Riding a cycle ergometer while experiencing virtual reality
|
|
Experimental: Cycle Ergometer
30 min ride on cycle ergometer
|
Riding on a cycle ergometer without experiencing virtual reality
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Beck Depression Inventory Scale of Measurement
Time Frame: 5 minutes
|
Assessment of symptoms of depression pre and post-intervention cycle exercise.
The Beck Depression Inventory is a 21-item, multiple-choice, self-report survey that measures characteristic attitudes and symptoms of depression.
The score range is 0-63.
The higher the score the more severe the depression.
Scores above 41 are considered "extreme depression."
|
5 minutes
|
|
Spatial Working Memory (SWM)
Time Frame: 8 minutes
|
A measure of the key aspects of working memory and storage of information over short periods of time.
|
8 minutes
|
|
Neuropsychological Outcomes: Motor Screen Tasks (MOT)
Time Frame: 3 minutes
|
MOT provides a general indication that psychomotor function is intact enough to proceed with more sophisticated cognitive testing:
|
3 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Neuropsychological Outcomes: MOT Mean Latency, MOT Total Correct, and MOT Total Errors
Time Frame: 10 minutes
|
This test is a general assessment of whether there are sensorimotor deficits or lack of comprehension.
Outcome is measured by reaction time in milliseconds of the participant reaching out and touching the "X" correctly (in the middle of the X) on the tablet in response to the stimulus.
The maximum score is 6000 milliseconds.
The number of total correct touches and total errors in not touching correctly out of 10 are recorded.
Ex: MOT mean latency = 927.9
ml +/- 131.43 ms; MOT Total Correct = 10; MOT Total Errors = 0.
|
10 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Judy R Wilson, Ph.D., UTArlington
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)
May 17, 2022
Primary Completion (Estimated)
August 31, 2027
Study Completion (Estimated)
August 31, 2027
Study Registration Dates
First Submitted
May 11, 2023
First Submitted That Met QC Criteria
July 31, 2023
First Posted (Actual)
August 2, 2023
Study Record Updates
Last Update Posted (Actual)
May 29, 2026
Last Update Submitted That Met QC Criteria
May 26, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020-0376
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
Yes
product manufactured in and exported from the U.S.
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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