- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03312790
Effects of Augmented Reality on Humans
October 12, 2017 updated by: Nicolas Babault, University of Burgundy
Effects of Augmented Reality Glasses on Muscle Activity, Balance, Physical and Mental Fatigue
Nowadays, augmented reality (AR) has gained attention but little is known concerning its repercussion in individuals when considering some mental and physiological aspects.
Therefore, the aim of this study was to investigate the effects of AR glasses on some cognitive and physiological functions in an attempt to determine its safety for workers.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Twelve volunteers were tested during two separate randomized sessions: one with AR glasses (ARGlass) and one in normal condition (Normal).
Participants had two perform different tasks of a 90 minutes total duration.
Before, during and after these tasks, two feet balance, one foot balance, precision balance, stroop and memory tests were performed.
Also, heart rate and electromyographic activity of some muscles were recorded.
Finally a survey was filled to determine, for example fatigue, pain or comfort.
Study Type
Interventional
Enrollment (Actual)
12
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
-
-
-
Dijon, France, 27877
- Centre d'Expertise de la Performance - Université de Bourgogne
-
-
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
18 years to 40 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- healthy
- BMI < 27
- physically active
- informed consent written form
Exclusion Criteria:
- in-habitual fatigue
- taking drugs and alcohol more than twice a day
- potential psychomotor disease
- injury in the preceding 3 months
- no healthcare
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: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: augmented reality device
Tasks realized using augmented reality device
|
Augmented reality device Real condition
Other Names:
|
Other: Real condition
Same tasks than augmented reality realized in normal/real condition
|
Augmented reality device Real condition
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Voluntary activation using electromyography of upper and lower limb muscles
Time Frame: Measured just before and immediately after every 30 minutes series (repeated three times)
|
The mean electromyographic activity of trapezius, deltoideus, biceps brachii, latissimus dorsi, soleus and tibialis anterior muscles will be measured using surface electrodes
|
Measured just before and immediately after every 30 minutes series (repeated three times)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Heart rate
Time Frame: Measured just before and immediately after every 30 minutes series (repeated three times)
|
Heart rate during the different tasks and test session
|
Measured just before and immediately after every 30 minutes series (repeated three times)
|
Balance
Time Frame: Measured just before and immediately after every 30 minutes series (repeated three times)
|
Two feet, one foot and precision tasks balance (center of pressure displacement)
|
Measured just before and immediately after every 30 minutes series (repeated three times)
|
Memory
Time Frame: Measured just before and immediately after every 30 minutes series (repeated three times)
|
5 words memory test
|
Measured just before and immediately after every 30 minutes series (repeated three times)
|
attention
Time Frame: Measured just before and immediately after every 30 minutes series (repeated three times)
|
Stroop test
|
Measured just before and immediately after every 30 minutes series (repeated three times)
|
subjective perceived exertion
Time Frame: Measured just before and immediately after every 30 minutes series (repeated three times)
|
difficulty of the tasks using a visual analogic scale
|
Measured just before and immediately after every 30 minutes series (repeated three times)
|
subjective pain perception
Time Frame: Measured just before and immediately after every 30 minutes series (repeated three times)
|
pain perceived (visual analogic scale) and the location if some pain sensation
|
Measured just before and immediately after every 30 minutes series (repeated three times)
|
subjective fatigue perception
Time Frame: Measured just before and immediately after every 30 minutes series (repeated three times)
|
perceived fatigue (visual analogic scale) and the location in case of fatigue feeling
|
Measured just before and immediately after every 30 minutes series (repeated three times)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
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)
February 1, 2017
Primary Completion (Actual)
February 15, 2017
Study Completion (Actual)
March 1, 2017
Study Registration Dates
First Submitted
June 13, 2017
First Submitted That Met QC Criteria
October 12, 2017
First Posted (Actual)
October 18, 2017
Study Record Updates
Last Update Posted (Actual)
October 18, 2017
Last Update Submitted That Met QC Criteria
October 12, 2017
Last Verified
October 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- CEP1701
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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