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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02980419
Other study ID # post_tilt_study
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 2016
Est. completion date May 31, 2020

Study information

Verified date December 2019
Source University of Zurich
Contact Dominik Straumann, MD
Phone +41442551111
Email dominik.straumann@usz.ch
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The long-term goal of this research is to advance the investigators knowledge of how the brain combines the information of multiple sensory systems coding for spatial oriention 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"). This effect could either be related to adaptation to the roll-tilted position (shifting the "null" position) or it could be related to changes in torsional eye position due to prolonged static roll-tilt (ocular counter-roll). While in the first case a post-tilt bias is predicted independently of the experimental paradigm used, the second hypothesis predicts a post-tilt bias only if retinal cues are integrated. In order to evaluate these hypotheses, the investigators will assess perceived vertical using both vision-dependent and vision-independent paradigms.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date May 31, 2020
Est. primary completion date May 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- ages 18-65 years

- informed consent

- absence of exclusion criteria

Exclusion Criteria:

- peripheral-vestibular deficit

- disturbed consciousness

- history of sensory deficits

- visual field deficits

- other neurological or systemic disorder which can cause dementia or cognitive dysfunction

- intake of antidepressants, sedatives, or neuroleptics

- pregnancy, unless excluded by a negative pregnancy test

- known neck pain or status post neck trauma

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
presentation of visual and vestibular stimuli
In each participant the investigators will assess verticality perception in whole-body upright position by use of the SVV, the SPV and the SHV after static roll-tilt at ±90deg over 5min. Measurements will be obtained on a motor-driven turntable and two different roll-tilt positions will be applied (±90°). A visual line (SVV), a rod (SHV) or the turntable itself will be adjusted to indicate perceived direction of vertical. A total of three measuring sessions, each lasting about 60 minutes are scheduled.

Locations

Country Name City State
Switzerland University Hospital Zurich, Dept. of Neurology Zurich ZH

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary adjustment errors of the subjective visual/haptic/postural vertical in upright position after prolonged whole-body roll-tilt positions. the accuracy and precision of visual vertical adjustments after prolonged roll tilt are quantified. 10 minutes (i.e. short-term adaptation)
Secondary changes in adjustment errors of the subjective visual vertical when providing an additional optokinetic stimulus This is the same as in outcome 1, but an additional visual (optokinetic) stimulus is added 10 minutes (i.e. short-term adaptation)
Secondary changes in adjustment errors of the subjective haptic vertical when providing an additional optokinetic stimulus This is the same as in outcome 1, but an additional visual (optokinetic) stimulus is added 10 minutes (i.e. short-term adaptation)
Secondary changes in adjustment errors of the subjective postural vertical when providing an additional optokinetic stimulus This is the same as in outcome 1, but an additional visual (optokinetic) stimulus is added 10 minutes (i.e. short-term adaptation)
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