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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03312790
Other study ID # CEP1701
Secondary ID
Status Completed
Phase N/A
First received June 13, 2017
Last updated October 12, 2017
Start date February 1, 2017
Est. completion date March 1, 2017

Study information

Verified date October 2017
Source University of Burgundy
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date March 1, 2017
Est. primary completion date February 15, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Device:
Tasks
Augmented reality device Real condition

Locations

Country Name City State
France Centre d'Expertise de la Performance - Université de Bourgogne Dijon

Sponsors (1)

Lead Sponsor Collaborator
University of Burgundy

Country where clinical trial is conducted

France, 

References & Publications (1)

Babault N, Païzis C, Deley G, Guérin-Deremaux L, Saniez MH, Lefranc-Millot C, Allaert FA. Pea proteins oral supplementation promotes muscle thickness gains during resistance training: a double-blind, randomized, Placebo-controlled clinical trial vs. Whey protein. J Int Soc Sports Nutr. 2015 Jan 21;12(1):3. doi: 10.1186/s12970-014-0064-5. eCollection 2015. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Voluntary activation using electromyography of upper and lower limb muscles 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 Heart rate Heart rate during the different tasks and test session Measured just before and immediately after every 30 minutes series (repeated three times)
Secondary Balance 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)
Secondary Memory 5 words memory test Measured just before and immediately after every 30 minutes series (repeated three times)
Secondary attention Stroop test Measured just before and immediately after every 30 minutes series (repeated three times)
Secondary subjective perceived exertion difficulty of the tasks using a visual analogic scale Measured just before and immediately after every 30 minutes series (repeated three times)
Secondary subjective pain perception 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)
Secondary subjective fatigue perception 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)
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