Determining the optimal dose of reactive balance training after stroke: study protocol for a pilot randomised controlled trial.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
26 08 2020
Historique:
entrez: 28 8 2020
pubmed: 28 8 2020
medline: 15 5 2021
Statut: epublish

Résumé

Falls risk poststroke is highest soon after discharge from rehabilitation. Reactive balance training (RBT) aims to improve control of reactions to prevent falling after a loss of balance. In healthy older adults, a single RBT session can lead to lasting improvements in reactive balance control and prevent falls in daily life. While increasing the dose of RBT does not appear to lead to additional benefit for healthy older adults, stroke survivors, who have more severely impaired balance control, may benefit from a higher RBT dose. Our long-term goal is to determine the optimal dose of RBT in people with subacute stroke. This assessor-blinded pilot randomised controlled trial aims to inform the design of a larger trial to address this long-term goal. Participants (n=36) will be attending out-patient stroke rehabilitation, and will be randomly allocated to one of three groups: one, three or six RBT sessions. RBT will replace a portion of participants' regular physiotherapy so that the total physical rehabilitation time will be the same for the three groups. Balance and balance confidence will be assessed at: (1) study enrolment; (2) out-patient rehabilitation discharge; and (3) 6 months postdischarge. Participants will report falls and physical activity for 6 months postdischarge. Pilot data will be used to plan the larger trial (ie, sample size estimate using fall rates, and which groups should be included based on between-group trends in pre-to-post training effect sizes for reactive balance control measures). Pilot data will also be used to assess the feasibility of the larger trial (ie, based on the accrual rate, outcome completion rate and feasibility of prescribing specific training doses). Institutional research ethics approval has been received. Study participants will receive a lay summary of results. We will also publish our findings in a peer-reviewed journal. NCT04219696; Pre results.

Identifiants

pubmed: 32847916
pii: bmjopen-2020-038073
doi: 10.1136/bmjopen-2020-038073
pmc: PMC7451480
doi:

Banques de données

ClinicalTrials.gov
['NCT04219696']

Types de publication

Clinical Trial Protocol Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e038073

Subventions

Organisme : CIHR
ID : MSH-141983
Pays : Canada

Informations de copyright

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Avril Mansfield (A)

Toronto Rehabilitation Institute - University Health Network, Toronto, Ontario, Canada avril.mansfield@uhn.ca.
Department of Physical Therapy, University of Toronto, Toronto, Ontario, Canada.
Evaluative Clinical Sciences, Hurvitz Brain Sciences Research Program, Sunnybrook Research Institute, Toronto, Ontario, Canada.

Elizabeth L Inness (EL)

Toronto Rehabilitation Institute - University Health Network, Toronto, Ontario, Canada.
Department of Physical Therapy, University of Toronto, Toronto, Ontario, Canada.

Cynthia J Danells (CJ)

Toronto Rehabilitation Institute - University Health Network, Toronto, Ontario, Canada.
Department of Physical Therapy, University of Toronto, Toronto, Ontario, Canada.

David Jagroop (D)

Toronto Rehabilitation Institute - University Health Network, Toronto, Ontario, Canada.

Tanvi Bhatt (T)

Department of Physical Therapy, University of Illinois, Chicago, Illinois, USA.

Andrew H Huntley (AH)

Toronto Rehabilitation Institute - University Health Network, Toronto, Ontario, Canada.

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