Internet-based vestibular rehabilitation versus standard care after acute onset vertigo: a study protocol for a randomized controlled trial.

AVS Acute onset vertigo Gait function Internet-based rehabilitation Multicenter Online tool Portable motion sensors RCT Randomized controlled trial Vestibular rehabilitation

Journal

Trials
ISSN: 1745-6215
Titre abrégé: Trials
Pays: England
ID NLM: 101263253

Informations de publication

Date de publication:
16 Jun 2022
Historique:
received: 25 12 2021
accepted: 09 06 2022
entrez: 16 6 2022
pubmed: 17 6 2022
medline: 22 6 2022
Statut: epublish

Résumé

Dizziness and vertigo affect around 15% of adults annually and represent common reasons for contacting health services, accounting for around 3% of all emergency department visits worldwide. Vertigo is also associated with excessive use of diagnostic imaging and emergency care and decreased productivity, primarily because of work absenteeism. Vestibular rehabilitation is an evidence-based treatment for chronic dizziness and supervised group exercise therapy has recently been shown to be effective after vestibular neuritis, a common cause of acute onset vertigo. However, such interventions are not readily available and there is a need for more easily accessible tools. The purpose of this study is to investigate the effects on vestibular symptoms of a 6-week online vestibular rehabilitation tool after acute onset vertigo, with the aim of aiding vestibular rehabilitation by presenting a more accessible tool that can help to reduce recovery time. Three hundred twenty individuals diagnosed with acute vestibular syndrome (AVS) will be recruited from multiple hospitals in Sweden and the effects of an online vestibular rehabilitation tool, YrselTräning, on vestibular symptoms after acute onset vertigo will be compared to standard care (written instructions leaflet) in a two-armed, evaluator-blinded, multicenter randomized controlled trial. The primary outcome will be the Vertigo Symptom Scale Short Form (VSS-SF) score at 6 weeks after symptom onset. Secondary outcomes include effects of the intervention on activities of daily living, mood and anxiety, vestibular function recovery, mobility measures, health economic effects, and the reliability of the Swedish VSS-SF translation. Participants using the online vestibular rehabilitation tool are expected to recover earlier and to a greater extent from their symptoms as compared to standard care. Since up to 50% of people with AVS without treatment develop persistent symptoms, effective treatment of AVS will likely lead to a higher quality of life and help reduce the societal costs associated with dizziness and vertigo. Clinicaltrials.gov NCT05056324 . Registered on September 24, 2021.

Sections du résumé

BACKGROUND BACKGROUND
Dizziness and vertigo affect around 15% of adults annually and represent common reasons for contacting health services, accounting for around 3% of all emergency department visits worldwide. Vertigo is also associated with excessive use of diagnostic imaging and emergency care and decreased productivity, primarily because of work absenteeism. Vestibular rehabilitation is an evidence-based treatment for chronic dizziness and supervised group exercise therapy has recently been shown to be effective after vestibular neuritis, a common cause of acute onset vertigo. However, such interventions are not readily available and there is a need for more easily accessible tools. The purpose of this study is to investigate the effects on vestibular symptoms of a 6-week online vestibular rehabilitation tool after acute onset vertigo, with the aim of aiding vestibular rehabilitation by presenting a more accessible tool that can help to reduce recovery time.
METHODS METHODS
Three hundred twenty individuals diagnosed with acute vestibular syndrome (AVS) will be recruited from multiple hospitals in Sweden and the effects of an online vestibular rehabilitation tool, YrselTräning, on vestibular symptoms after acute onset vertigo will be compared to standard care (written instructions leaflet) in a two-armed, evaluator-blinded, multicenter randomized controlled trial. The primary outcome will be the Vertigo Symptom Scale Short Form (VSS-SF) score at 6 weeks after symptom onset. Secondary outcomes include effects of the intervention on activities of daily living, mood and anxiety, vestibular function recovery, mobility measures, health economic effects, and the reliability of the Swedish VSS-SF translation.
DISCUSSION CONCLUSIONS
Participants using the online vestibular rehabilitation tool are expected to recover earlier and to a greater extent from their symptoms as compared to standard care. Since up to 50% of people with AVS without treatment develop persistent symptoms, effective treatment of AVS will likely lead to a higher quality of life and help reduce the societal costs associated with dizziness and vertigo.
TRIAL REGISTRATION BACKGROUND
Clinicaltrials.gov NCT05056324 . Registered on September 24, 2021.

Identifiants

pubmed: 35710448
doi: 10.1186/s13063-022-06460-0
pii: 10.1186/s13063-022-06460-0
pmc: PMC9205069
doi:

Banques de données

ClinicalTrials.gov
['NCT05056324']

Types de publication

Clinical Trial Protocol Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

496

Subventions

Organisme : Vetenskapsrådet
ID : 2020-00301

Informations de copyright

© 2022. The Author(s).

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Auteurs

Solmaz Surano (S)

Department of Clinical Sciences, Neurosciences, Umeå University, Umeå, Sweden.

Helena Grip (H)

Department of Radiation Sciences, Umeå University, Umeå, Sweden.
Department of Biomedical Engineering, Umeå University, Umeå, Sweden.

Fredrik Öhberg (F)

Department of Radiation Sciences, Umeå University, Umeå, Sweden.
Department of Biomedical Engineering, Umeå University, Umeå, Sweden.

Marcus Karlsson (M)

Department of Clinical Sciences, Neurosciences, Umeå University, Umeå, Sweden.
Department of Biomedical Engineering, Umeå University, Umeå, Sweden.

Erik Faergemann (E)

Department of Clinical Sciences, Neurosciences, Umeå University, Umeå, Sweden.
Sundsvall Regional Hospital, Sundsvall, Sweden.

Maria Bjurman (M)

Sollefteå Hospital, Region Västernorrland, Sollefteå, Sweden.

Hugo Davidsson (H)

Department of Otorhinolaryngology, Head and Neck Surgery, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Department of Otorhinolaryngology, Head and Neck Surgery, Region Västra Götaland, Sahlgrenska University Hospital, Gothenburg, Sweden.

Torbjörn Ledin (T)

Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.

Ellen Lindell (E)

Department of Otorhinolaryngology, Head and Neck Surgery, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Department of Otorhinolaryngology, Region Västra Götaland, Södra Älvsborg Hospital, Borås, Sweden.

Jan Mathé (J)

Department of Clinical Neuroscience, Karolinska Institutet and Capio S:t Görans Hospital, Stockholm, Sweden.

Fredrik Tjernström (F)

Department of Clinical Sciences, Othorhinolaryngology, Lund University, Lund, Sweden.

Tatjana Tomanovic (T)

Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.

Gabriel Granåsen (G)

Department of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden.

Jonatan Salzer (J)

Department of Clinical Sciences, Neurosciences, Umeå University, Umeå, Sweden. jonatan.salzer@umu.se.

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Classifications MeSH