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Subjective Visual VerticalNCT03377166

Measuring Subjective Visual Vertical (SVV) Using a Smartphone Application

A study testing Bucket test and Smartphone-based evaluation of SVV in people with Subjective Visual Vertical, run by Tel-Aviv Sourasky Medical Center at 1 site in Israel.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

A comparison between two methods evaluating SVV: Bucket Test and A smartphone-based test. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Subjective Visual Vertical
What is being tested?
Bucket test and Smartphone-based evaluation of SVV
Could I receive a placebo?
No, everyone receives an active treatment
How many people
45 participants
Where
1 siteIsrael
Study dates
1 Jan 2018to 19 Dec 2018
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Vestibular Disorder

Who cannot join

  • Chronic ear disease, Neurological disorder, s/p Ear surgery

Trial locations and contacts

1 site in 1 country.

Israel1 site
  • The Tel Aviv Sourasky Medical Center

    Tel Aviv

Other trials in Israel

About this study

A comparison between two methods evaluating SVV: Bucket Test and A smartphone-based test.

Being tested
Bucket test and Smartphone-based evaluation of SVV

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Bucket test and Smartphone-based evaluation of SVVDiagnostic test

    Bucket test and Smartphone-based evaluation of SVV

Study groups in NCT03377166
Study groupRoleWhat they receive
VertigoActive comparatorParticipants with vestibular disorder
Receives: Diagnostic Test: Bucket test and Smartphone-based evaluation of SVV
ControlActive comparatorParticipants without vestibular disorder
Receives: Diagnostic Test: Bucket test and Smartphone-based evaluation of SVV

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Results of Bucket test Smartphone-based evaluation of SVV

    Measured: 5 minutes

  2. Results of Smartphone-based evaluation of SVV

    Measured: 5 minutes

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Dec 2017
  2. Study start1 Jan 2018
  3. Primary completion19 Dec 2018
  4. Study completion19 Dec 2018

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Diagnosis
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
45 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03377166
Sponsor's protocol ID
0113-17-TLV
Status last verified
Jan 2019
First submitted
7 Dec 2017
Last updated
11 Jan 2019
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Bucket test and Smartphone-based evaluation of SVV in people with Subjective Visual Vertical, run by Tel-Aviv Sourasky Medical Center at 1 site in Israel.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 11 Jan 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Israel. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Results of Bucket test Smartphone-based evaluation of SVV (time frame: 5 minutes). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Jan 2019; AzTrials last refreshed its copy on 4 Nov 2026.

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