Verticality Perception - Effects of Prolonged Roll-tilt in Healthy Human Subjects

NCT ID: NCT02760173

Last Updated: 2018-07-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Clinical Phase

NA

Study Classification

INTERVENTIONAL

Study Start Date

2016-06-01

Study Completion Date

2018-06-28

Brief Summary

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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.

Detailed Description

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Conditions

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Vestibular Perception

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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Single intervention arm

This is the only arm in this study, measuring verticality perception after prolonged roll-tilt over 5min.

Group Type EXPERIMENTAL

perception of vertical after static roll-tilt over 5min

Intervention Type OTHER

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

Interventions

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perception of vertical after static roll-tilt over 5min

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

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

1. ages 18-65 years
2. informed consent

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
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Zurich

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Dominik Straumann, MD

Role: PRINCIPAL_INVESTIGATOR

University of Zurich, Switzerland

Other Identifiers

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vert_perc_posttilt

Identifier Type: -

Identifier Source: org_study_id

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