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HealthyNCT07129876

Motion Fidelity Effects With Mixed-Reality

A study testing Simulator Motion in people with Healthy, run by National Aeronautics and Space Administration (NASA) at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this research is to investigate how different levels of simulator motion fidelity affect pilot performance in two different flight tasks while using a head mounted display (or mixed-reality headset) for out-the-window (OTW) visuals. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Healthy
What is being tested?
Simulator Motion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
13 participants
Where
1 siteUnited States
Study dates
19 May 2025to 30 May 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Normal or corrected to normal vision.

Who cannot join

  • Claustrophobia.
  • Susceptible to motion sickness.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • NASA Ames Research Center, Vertical Motion Simulator

    Mountain View, California, 94035

Other trials in United States

About this study

Official title: Effects of Simulator Motion Fidelity on Pilot Performance While Using a Mixed-Reality Headset

The purpose of this research is to investigate how different levels of simulator motion fidelity affect pilot performance in two different flight tasks while using a head mounted display (or mixed-reality headset) for out-the-window (OTW) visuals. Three levels of motion fidelity will be studied: 1) no motion, 2) small hexapod motion, and 3) one-to-one vehicle motion.

Read the detailed description

The aim of this study is to determine the effects of simulator motion fidelity on pilot performance in two demanding piloting tasks while wearing a mixed-reality headset for OTW visuals. Pilots will be exposed to mixed-reality visuals meaning that the virtual OTW visual scene will be overlayed on an image of the real simulator cockpit and head down displays (HDD). Pilots will fly two tasks in this experiment: 1) a roll-lateral sidestep maneuver, and 2) a precision landing.

In task 1, the roll-lateral sidestep maneuver will be from one landing pad to a second landing pad of a vertiport on the Fifth \& Mission Parking Garage in San Francisco. The vertiport is in a San Francisco visual database surrounded by buildings with high-resolution textures. Pilots are instructed to stay at a constant altitude. A positioning sight will be placed in the visual scene at each landing pad to allow pilots to determine their positioning error precisely. Pilots will be provided with lateral position and time criteria for desired and adequate performance. Pilots will be instructed to press an event marker on their control inceptor when they acquire the station-keeping point at the landing pad. Turbulence will be used to make the task more difficult. This task will be similar to the roll-lateral experiment described by Schroeder that was also performed in the VMS.

In task 2, pilots will perform a landing at the same vertiport in San Francisco that is used in task 1. The task will start from level flight from a position that allows for a standard approach and landing. Landing position and time criteria for desired and adequate performance will be communicated to the pilots. Pilots will press an event marker on the control inceptor when they acquire the desired reference point on the landing pad. Turbulence will be introduced to make the task more difficult.

Pilots will receive the informed consent form and a Motion Sickness Susceptibility Questionnaire (MSSQ via email first. They will be asked to fill out the MSSQ at home and return it to the PI before being scheduled and coming to the VMS. On the day of the experiment, participants will first receive a briefing and walkaround of the facility before providing their informed consent (60 minutes). Next, they will take a seat in the simulator cab where seat and headset adjustments will be made first to make sure the experiment can be performed comfortably. This is followed by the first data-collection session in which one of the tasks is flown (45 minutes). Both tasks will be flown under three motion fidelity conditions described in Section 8.3 below. Three repetitions of each motion condition will be flown for both tasks, after completing three training runs, for a total of 12 runs per task. A 30-minute break is scheduled after the first data-collection session. The second session in which the other tasks is flown will commence after the break (45 minutes). Finally, pilots will be debriefed and can ask any remaining questions (30 minutes).

Pilot performance in each task will be determined by several outcome-based variables, including the error between desired and actual aircraft position and attitude at specified locations, the intensity of control inputs, and task completion time. Pilots will also complete a motion fidelity rating and a Simulator Sickness Questionnaire (SSQ) at the end of each run.

Hypothesis: Pilot performance and subjective motion ratings will be significantly different between the different simulator motion fidelity conditions.

Before data analysis, all data will be averaged over the three repetitions of each condition. A one-way repeated-measures Multivariate Analysis of Variance (MANOVA) will be used on the data from each task to determine statistically significant effects. If test assumptions are not met (e.g., homogeneity of covariance matrices), corrections or appropriate alternate tests will be used. Any reporting of the statistical results will include the F statistic (or equivalent for alternate tests), degrees of freedom, probability values, and effect sizes.

Based on previous studies investigating the effects of motion fidelity on pilot performance, it is expected that pilot performance will be lower without simulator motion or with small-hexapod motion compared to one-to-one vehicle motion. Control intensity will show the opposite trend; that is, will be higher without simulator motion and will decrease with higher motion fidelity.

Conditions
Healthy
Being tested
Simulator Motion

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Simulator MotionOther

    Motion fidelity of the simulator.

Study groups in NCT07129876
Study groupRoleWhat they receive
Simulator Motion VariationsExperimental2 flight tasks; 4 motion conditions; 3 repetitions per condition (n = 12 per task)
Receives: Other: Simulator Motion

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Time to Complete Flight Task Maneuver (Averaged over Repetitions)

    Time needed to complete (a portion of) the flight task measured against desired and adequate performance criteria:

    Heliport Approach Task - Battery time remaining (desired >=20:00 min, adequate >=19:40 min)

    Lateral Reposition and Hold Task

    • Reposition completion time (desired <=25 s, adequate <=35 s)

    Measured: Day 1

  2. Accuracy of the Flight Task Maneuver (Averaged over Repetitions)

    Accuracy of the maneuver during (a portion of) the flight task measured against desired and adequate performance criteria:

    Heliport Approach Task

    • Glideslope deviation (desired +-0.7 deg, adequate +-2.1 deg)
    • Localizer deviation (desired +-0.7 deg, adequate +-2.1 deg)
    • Helipad boundary crossing height (desired +-10 ft, adequate +-20 ft)
    • Helipad boundary crossing speed (desired +-5 kts, adequate +-10 kts)
    • Helipad center deviation (desired +-20 ft, adequate +-60 ft)

    Lateral Reposition and Hold Task

    • Ground track deviation (desired +-5 ft, adequate +-10 ft)
    • Target ground speed deviation (desired +-5 kts, adequate +-8 kts)
    • Altitude deviation (desired +-5 ft, adequate +-10 ft)
    • Heading deviation (desired +-10 deg, adequate +-15 deg)
    • Hover point lateral and longitudinal deviation (desired +-5 ft, adequate +-10 ft)

    Measured: Day 1

  3. Motion Fidelity Rating

    Possible answers are: Low Fidelity, Medium Fidelity, High Fidelity

    Measured: Day 1

Secondary outcomes (1)
  1. Simulator Sickness Questionnaire (SSQ)

    This questionnaire requires rating 16 symptoms with a scale from none, slight, moderate, to severe. The symptoms are: general discomfort, fatigue, headache, eye strain, difficulty focusing, increased salivation, sweating, nausea, difficulty concentrating, fullness of head, blurred vision, dizzy (eyes open), dizzy (eyes closed), vertigo, stomach awareness, burping.

    Measured: Day 1

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Aug 2025
  2. Study start19 May 2025
  3. Primary completion30 May 2025
  4. Study completion30 May 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
13 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07129876
Sponsor's protocol ID
STUDY00000883
Status last verified
Apr 2026
First submitted
5 Jun 2025
Last updated
13 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Simulator Motion in people with Healthy, run by National Aeronautics and Space Administration (NASA) at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 13 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Time to Complete Flight Task Maneuver (Averaged over Repetitions) (time frame: Day 1). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Apr 2026.

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