Effects of Augmented Reality on Humans

NCT03312790 | Completed

• 1 other identifier: CEP1701
• Study Type: interventional
• Target: 12
• Locations: 1 country
• Sites: 1

Brief 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.

Conditions

Physical Activity; Mental Status Change

Keywords

augmented reality; fatigue; muscle; heart rate; mental function

Outcome Measures

Primary Outcomes (1)

• 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 Outcomes (7)

• Heart rate

  Measured just before and immediately after every 30 minutes series (repeated three times)

• Balance

  Measured just before and immediately after every 30 minutes series (repeated three times)

• Memory

  Measured just before and immediately after every 30 minutes series (repeated three times)

• attention

  Measured just before and immediately after every 30 minutes series (repeated three times)

• subjective perceived exertion

  Measured just before and immediately after every 30 minutes series (repeated three times)

Study Arms (2)

augmented reality device

EXPERIMENTAL

Tasks realized using augmented reality device

Device: Tasks

Real condition

OTHER

Same tasks than augmented reality realized in normal/real condition

Device: Tasks

Interventions

Tasks DEVICE

Augmented reality device Real condition

Also known as: Workers tasks

Real condition; augmented reality device

Eligibility Criteria

• Age: 18 Years - 40 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• healthy
• BMI \< 27
• physically active
• informed consent written form

You may not qualify if:

• in-habitual fatigue
• taking drugs and alcohol more than twice a day
• potential psychomotor disease
• injury in the preceding 3 months
• no healthcare

Sponsors & Collaborators

• University of Burgundy: lead

Study Sites (1)

Centre d'Expertise de la Performance - Université de Bourgogne

Dijon, 27877, France

Location

Related Publications (1)

• Babault N, Paizis C, Deley G, Guerin-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.

  PMID: 25628520 BACKGROUND

Related Links

• centre d'expertise de la performance

MeSH Terms

Conditions

Motor Activity; Fatigue

Condition Hierarchy (Ancestors)

Behavior; Signs and Symptoms; Pathological Conditions, Signs and Symptoms

Study Officials

• Nicolas Babault, PhD

  University of Burgundy

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: OUTCOMES ASSESSOR
• Purpose: BASIC SCIENCE
• Intervention Model: CROSSOVER
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: principal investigator

Study Record Dates

• First Submitted: June 13, 2017
• First Posted: October 18, 2017
• Study Start: February 1, 2017
• Primary Completion: February 15, 2017
• Study Completion: March 1, 2017
• Last Updated: October 18, 2017

Record last verified: 2017-10

Data Sharing

• IPD Sharing: Will not share

Locations

FR (1)