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Assessment of fixation suppression of the vestibulo-ocular reflex with videooculography and smartphone

Assessment of fixation suppression of the vestibulo-ocular reflex with videooculography and smartphone - VOR-S-martphone

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00013968
Enrollment
40
Registered
2018-02-22
Start date
2015-11-20
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

G23.3 G23.2 R27.0

Interventions

Group 1: Assessment of fixation suppression of the vestibulo-ocular reflex (FS-VOR) using videooculography and a smartphone

Sponsors

Kliniken Beelitz GmbH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: patients undergoing videooculography for assessment fo fixation suppression of vestibule-ocular reflex; patients willing to give written informed consent to participate in this trial

Exclusion criteria

Exclusion criteria: patients not capable to understand the content of this trial, pregnancy

Design outcomes

Primary

MeasureTime frame
The fixation suppression of the vestibulo-ocular reflex can be assessed as easily and accurate as done by video-oculography. Therefore, aach participant will once undergo testing of the fixation suppression of the vestibulo-ocular reflex with both videooculography and the smartphone method. Videooculography, as the gold standard, will be used to assess whether fixation suppression is pathological, and the result will be compared with the smartphone method. The hypothesis is that when comparing test results, both methods are equally exact in differentiating normal from pathological fixation suppression.

Secondary

MeasureTime frame
Inter-Rater reliability

Countries

Germany

Contacts

Public ContactFlorin Gandor

Neurologisches Fachkrankenhaus für Bewegungsstörungen/Parkinson

gandor@kliniken-beelitz.de+49-33204-22781

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026