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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02980432
Other study ID # shv_okn_study
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 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 investigators previously shown that a rotating optokinetic stimulus results in shifts of the subjective visual vertical in healthy human subjects. However, the origin of these shifts is still poorly understood. Both torsional displacement of the eyes and a shift in the internal estimate of direction of gravity have been proposed as potential explanations. Here the investigators use a vision-independent setup to differentiate between these two hypotheses, predicting no impact of a rotating stimulus on the subjective haptic vertical if torsion triggers the shift.


Recruitment information / eligibility

Status Completed
Enrollment 19
Est. completion date June 28, 2018
Est. primary completion date June 1, 2018
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

Other:
changes in whole-body roll position and visual/haptic stimuli presented
In different whole-body roll positions subjects will be presented a luminous line or a rod in combination with a moving or stationary background. Participants will be asked to align the line or the rod along perceived direction of gravity.

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 aligning a rod along perceived direction of gravity while an optokinetic stimulus is presented. This outcome parameter focuses on the adjustment errors of the subjective haptic vertical while presenting a visual bias (i.e. an optokinetic rotatory stimulus). 60 minutes
Primary Trial-to-trial variability of aligning a rod along perceived direction of gravity while an optokinetic stimulus is presented. This outcome parameter focuses on the trial-to-trial variability of rod alignments along perceived direction of gravity when presenting a visual bias cue (i.e. an optokinetic rotatory stimulus). 60 minutes
Secondary Comparison of adjustment errors between the subjective haptic vertical and the subjective visual vertical 60 minutes
Secondary Comparison of adjustment errors of perceived vertical using the subjective haptic vertical with and without presenting an optokinetic stimulus 60 minutes
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