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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02760173
Other study ID # vert_perc_posttilt
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date June 1, 2016
Est. completion date June 28, 2018

Study information

Verified date June 2018
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The long-term goal of this research is to advance our knowledge of how the brain combines the information of multiple sensory systems coding for spatial orientation and how adaptation to vestibular imbalance influences spatial orientation. In healthy human subjects verticality perception is accurate while upright. After prolonged roll-tilt, humans show a systematic bias in perceived direction towards the previous roll-tilted position (so-called "post-tilt bias"). Here we evaluate different potential explanations for this bias using both vision-dependent and vision-independent paradigms of verticality perception.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date June 28, 2018
Est. primary completion date July 1, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

1. ages 18-65 years

2. informed consent

3. absence of exclusion criteria

Exclusion Criteria:

1. peripheral-vestibular deficit

2. disturbed consciousness

3. history of sensory deficits

4. visual field deficits

5. other neurological or systemic disorder which can cause dementia or cognitive dysfunction

6. intake of antidepressants, sedatives, or neuroleptics

7. pregnancy, unless excluded by a negative pregnancy test

8. known neck pain or status post neck trauma

Study Design


Related Conditions & MeSH terms


Intervention

Other:
perception of vertical after static roll-tilt over 5min
subjects will indicate perceived direction of vertical after 5min of static whole-body roll-tilt.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Outcome

Type Measure Description Time frame Safety issue
Primary Adjustment errors and trial-to-trial variability as assessed by line adjustments (subjective visual vertical (SVV)), adjustments of a rod (subjective haptic vertical (SHV)) or self-adjustments (subjective postural vertical (SPV)) after prolonged roll In all three paradigms (SVV, SHV and SPV) the percept of direction of gravity will be assessed. Parameters will be adjustment errors ("accuracy") and trial-to-trial variability ("precision") based on repetitive adjustments of a luminous line (SVV) or a rod (SHV) after returning to upright position after a period of 5min in static roll-tilt at 90° left-ear down or right-ear down. During the roll-tilt period subjects remain either in the dark or observe a rotating optokinetic (random dot) pattern. Individual mean values and standard deviation (SD) will be calculated for all conditions. Adjustments with the joystick (SPV) will start from 90° ear-down positions after 5min of static roll. measurements will be obtained over periods of 5min in a single session and day
Secondary Impact of a rotating optokinetic stimulus (velocity 60°/s) on adjustment errors as assessed by the SVV, the SHV or the SPV after 5min of static roll-tilt at +/- 90° roll. During the 5min period with static roll at +/- 90deg ear-down positions subjects will be presented a rotating optokinetic stimulus (random dot pattern, clockwise or counter-clockwise rotation) in some conditions. Adjustment errors and trial-to-trial variability of conditions with the optokinetic stimulus will be compared to those without the optokinetic stimulus. measurements will be obtained over periods of 5min in a single session and day
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