Vestibular rehabilitation practice in neurorehabilitation: an Italian survey protocol

Abstract

Introduction Neurological disorders are a prevalent cause of disability and death, which has a considerable impact on the world's economic and healthcare systems, not least because of rehabilitation needs. Neurorehabilitation is effective and recommended for the best recovery of motor and cognitive functions and quality of life. This study evaluates clinicians' perceptions of vestibular rehabilitation's actual or potential role in neurorehabilitation. Methods This is the protocol for a cross-sectional study that will be conducted as an online survey approved by the University of Bologna Bioethics Committee. The survey lasts approximately 10 minutes and consists of 4 main sections (socio-demographic, professional, clinical, and future recommendation data), with a total of 27 closed questions and 2 open questions. 5 experts constructed the questionnaire, and then 6 respondents piloted it; these latter were representative of the subjects to whom it will be administered. We will report the Survey following the Checklist for Reporting Of Survey Studies (CROSS). Expected results This questionnaire will map the knowledge and use of vestibular rehabilitation in neurorehabilitation by healthcare professionals in Italy. It will also be interesting to assess possible gaps, challenges, and research perspectives on this prevalent topic.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This research received no specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

The Bioethics Committee of the University of Bologna gave ethical approval for this work.

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

All data produced in the present study are available upon reasonable request to the authors.

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