An interventional study of Tasks in Physical Activity and Mental Status Change, sponsored by University of Burgundy. Completed at 1 site in France. Open to participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-10-18.
Sponsored by University of Burgundy · Not applicable, Interventional, and Basic science
Among 104 studies in Fatigue with a site in France — 33 open to participants now, 36 under way, 3 of them phase 3. Fatigue · France.
Among the 104 studies in Fatigue with a site in France, this one is the 68th largest by enrollment of the 72 interventional ones that give a count, is one of 6 that started in 2017, is one of 61 with no phase, and was the 27th registered.
2,229 studies on the registry are indexed under Fatigue; 426 are open to participants now.
Browse Fatigue studies →33 of the 104 studies in Fatigue with a site in France are open now. Recruiting first, the newest first:
Centre Antoine Lacassagne · Sites in France
Novartis Pharmaceuticals · Sites in France, United States, Australia and 17 more countries
Centre Medical ISM (Integrative Systemic Medicine) · Sites in France
Alkermes, Inc. · Sites in France, United States, Australia and 7 more countries
Centre Hospitalier Universitaire de Saint Etienne · Sites in France
A study can be open while its sites in France have not opened yet or have stopped. Only those recruiting at a site in France →
Of the 240 Fatigue studies recruiting now, 112 (47%) set no upper age limit and 98 (41%) stop at 75 or younger; 24 take children under 18; 74 take healthy volunteers.
This study: 18 Years to 40 Years · all sexes · healthy volunteers too.
The full table on the hub →This tab as a report to print or save as PDF → With an account.
104 studies; the count open now beside each. This study's row is marked.
A study in two phases is counted once above. Listed by phase, each with its combined phases: Phase 2 6 · Phase 3 5 · Phase 4 2
First in 2005; this study’s year is marked. 6 started in 2017.
This study's enrollment of 12 is below the median of 54 across 1,757 interventional studies indexed under Fatigue.
Median enrollment 70 across the 72 interventional studies, 60 across the 32 observational. Of the 57 that completed or were terminated, 4 (7%) have results posted.
This tab as a report to print or save as PDF → With an account.
10 of 104 have an industry lead sponsor. The 10 most frequent:
University of Burgundy is the lead sponsor of 12 studies on the registry; 2 are open to participants now.
University of Burgundy has 2 studies filed under Fatigue — fewer than ten, so there is no comparison to draw.
9 of the studies in Fatigue with a site in France that are under way reach primary completion within a year, 1 of them phase 3. Phase 3 first, then by date:
| Study | Primary completion |
|---|---|
| NCT07455383Phase 3Alkermes, Inc.A Study to Evaluate the Efficacy and Safety of ALKS 2680 in Adults With Narcolepsy Type 1 | 2027-05 |
| NCT07054112University Hospital, ToursEfficacy of Live Online Course Mindfulness Program on Perceived Fatigue in Hemodialysis Patients | 2026-11-30 |
| NCT07310342University Hospital, BordeauxPhysical Fitness of Children, Adolescents and Young Adults With Immune Thrombocytopenic Purpura | 2026-12-15 |
| NCT07278973AUB SantéHemodiafiltration Versus Hemodialysis in Older People | 2026-12-19 |
| NCT07637084Centre Medical ISM (Integrative Systemic Medicine)Photobiomodulation for Chronic Pain and Fatigue in Hypermobile Ehlers-Danlos Syndrome (PBM-SEDh-01) | 2027-03-31 |
Among the 104 studies in Fatigue with a site in France, from their registry updates:
This tab as a report to print or save as PDF → With an account.
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.
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.
2,229 studies on the registry are indexed under Fatigue; 426 are open to participants now.
This study's enrollment of 12 is below the median of 54 across 1,757 interventional studies indexed under Fatigue.
Browse Fatigue studies →University of Burgundy is the lead sponsor of 12 studies on the registry; 2 are open to participants now.
Compared within Fatigue, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Motor Activity. The counts are of registry records indexed under each term, refreshed daily. How we classify →
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.
What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
BMI (body mass index)
Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.
What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Tasks realized using augmented reality device
Device: Tasks
Same tasks than augmented reality realized in normal/real condition
Device: Tasks
Augmented reality device Real condition
Also known as: Workers tasks
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
Time frame: Measured just before and immediately after every 30 minutes series (repeated three times)
Heart rate
Heart rate during the different tasks and test session
Time frame: Measured just before and immediately after every 30 minutes series (repeated three times)
Balance
Two feet, one foot and precision tasks balance (center of pressure displacement)
Time frame: Measured just before and immediately after every 30 minutes series (repeated three times)
Memory
5 words memory test
Time frame: Measured just before and immediately after every 30 minutes series (repeated three times)
attention
Stroop test
Time frame: Measured just before and immediately after every 30 minutes series (repeated three times)
subjective perceived exertion
difficulty of the tasks using a visual analogic scale
Time frame: Measured just before and immediately after every 30 minutes series (repeated three times)
subjective pain perception
pain perceived (visual analogic scale) and the location if some pain sensation
Time frame: Measured just before and immediately after every 30 minutes series (repeated three times)
subjective fatigue perception
perceived fatigue (visual analogic scale) and the location in case of fatigue feeling
Time frame: Measured just before and immediately after every 30 minutes series (repeated three times)
Plan to share: No
Ran from Feb 2017 to primary completion in Feb 2017, 0 months.
Of 936 non-industry interventional studies with no phase under Fatigue, half reached primary completion within 12 months of starting (the median), counting those still running; a quarter within 5 and three quarters within 27. This study's 0 months is below that.
Counting every sponsor, half of 989 studies reached it within 11 months; a quarter within 5 and three quarters within 27.
How these figures are worked out, and which studies are left out of them.
This study is completed, as verified in Oct 2017. You cannot join it, but the record below documents what was studied.
Get an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.
University of Burgundy