Stroke Clinical Trial
Official title:
Feasibility and Safety of a Telemedically Performed Three-Component Oculomotor Testing Battery (HINTS) in Healthy Adults
The study investigates the feasibility and safety of the telemedical implementation of three
diagnostic oculomotor tests using a video-oculography device and an extended
teleconferencing system. The testing battery comprises Halmagyi's head impulse test, test
for nystagmus and test of skew (vertical misalignment) known as the HINTS protocol.
Previously published data have shown high sensitivity and specificity of the protocol for
the discrimination of central and peripheral causes of acute vestibular syndrome. In this
study the three tests will be executed on 30 healthy subjects using video goggles
(EyeSeeCam, Interacoustics GmbH, Germany) connected to a mobile wireless-workstation for
bidirectional audiovisual communication in a clinical environment (MEYTEC GmbH, Germany). A
newly developed remote control and video conferencing solution allows the execution and
evaluation of the HINTS protocol in a telemedical setup.
The examination is guided by a remote physician using the help of a trained assistant
attending to the subject. Corresponding clinical bedside tests will be executed for
comparison. Primary endpoint is feasibility of the three diagnostic tests in a telemedical
setting. Safety as well as accuracy of the telemedical versus bedside examination will be
analyzed as secondary outcome measures. Aim of the study is to improve diagnostic accuracy
for patients with acute vestibular syndrome in remote areas where specialists are rare.
Status | Completed |
Enrollment | 30 |
Est. completion date | December 2016 |
Est. primary completion date | December 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Consenting adults Exclusion Criteria: - Acute vertigo or dizziness, acute neck pain, history of stroke, history of acute vestibular syndrome, strong unilateral or bilateral visual impairment, complete movement restriction of cervical spine |
Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic
Country | Name | City | State |
---|---|---|---|
Germany | Klinikum München-Harlaching | Munich | Bavaria |
Lead Sponsor | Collaborator |
---|---|
Munich Municipal Hospital |
Germany,
Bartl K, Lehnen N, Kohlbecher S, Schneider E. Head impulse testing using video-oculography. Ann N Y Acad Sci. 2009 May;1164:331-3. doi: 10.1111/j.1749-6632.2009.03850.x. — View Citation
Kattah JC, Talkad AV, Wang DZ, Hsieh YH, Newman-Toker DE. HINTS to diagnose stroke in the acute vestibular syndrome: three-step bedside oculomotor examination more sensitive than early MRI diffusion-weighted imaging. Stroke. 2009 Nov;40(11):3504-10. doi: 10.1161/STROKEAHA.109.551234. — View Citation
MacDougall HG, Weber KP, McGarvie LA, Halmagyi GM, Curthoys IS. The video head impulse test: diagnostic accuracy in peripheral vestibulopathy. Neurology. 2009 Oct 6;73(14):1134-41. doi: 10.1212/WNL.0b013e3181bacf85. — View Citation
Newman-Toker DE, Kerber KA, Hsieh YH, Pula JH, Omron R, Saber Tehrani AS, Mantokoudis G, Hanley DF, Zee DS, Kattah JC. HINTS outperforms ABCD2 to screen for stroke in acute continuous vertigo and dizziness. Acad Emerg Med. 2013 Oct;20(10):986-96. doi: 10.1111/acem.12223. — View Citation
Newman-Toker DE, Saber Tehrani AS, Mantokoudis G, Pula JH, Guede CI, Kerber KA, Blitz A, Ying SH, Hsieh YH, Rothman RE, Hanley DF, Zee DS, Kattah JC. Quantitative video-oculography to help diagnose stroke in acute vertigo and dizziness: toward an ECG for the eyes. Stroke. 2013 Apr;44(4):1158-61. doi: 10.1161/STROKEAHA.111.000033. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of evaluable telemedical oculomotor examinations | through completion of diagnostic test, an average of 10 minutes | No | |
Secondary | Accuracy of telemedical oculomotor examination (correlation to bedside test) | through completion of diagnostic test, an average of 10 minutes | No | |
Secondary | Number of participants with adverse or serious adverse events that are related to telemedical oculomotor examination | through completion of diagnostic test, an average of 10 minutes | Yes | |
Secondary | Time delay of telemedical tests | through completion of diagnostic test, an average of 10 minutes | No |
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