Cargando…
Mobile health to promote physical activity in people post stroke or transient ischemic attack – study protocol for a feasibility randomised controlled trial
BACKGROUND: Physical activity is essential to improve health and reduce the risk of recurrence of stroke or transient ischemic attack (TIA). Still, people post stroke or TIA are often physically inactive and the availability of physical activity promotion services are often limited. This study build...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043533/ https://www.ncbi.nlm.nih.gov/pubmed/36978045 http://dx.doi.org/10.1186/s12883-023-03163-0 |
_version_ | 1784913176113971200 |
---|---|
author | Thurston, Charlotte Bezuidenhout, Lucian Humphries, Sophia Johansson, Sverker von Koch, Lena Häger, Charlotte K. Holmlund, Lisa Sundberg, Carl Johan Garcia-Ptacek, Sara Kwak, Lydia Nilsson, Michael English, Coralie Conradsson, David Moulaee |
author_facet | Thurston, Charlotte Bezuidenhout, Lucian Humphries, Sophia Johansson, Sverker von Koch, Lena Häger, Charlotte K. Holmlund, Lisa Sundberg, Carl Johan Garcia-Ptacek, Sara Kwak, Lydia Nilsson, Michael English, Coralie Conradsson, David Moulaee |
author_sort | Thurston, Charlotte |
collection | PubMed |
description | BACKGROUND: Physical activity is essential to improve health and reduce the risk of recurrence of stroke or transient ischemic attack (TIA). Still, people post stroke or TIA are often physically inactive and the availability of physical activity promotion services are often limited. This study builds on an existing Australian telehealth-delivered programme (i-REBOUND– Let’s get moving) which provides support for home-based physical activity for people post stroke or TIA. The aim of this study is to test the feasibility, acceptability, and preliminary effects of a mobile Health (mHealth) version of the i-REBOUND programme for the promotion of physical activity in people post stroke or TIA living in Sweden. METHODS: One hundred and twenty participants with stroke or TIA will be recruited via advertisement. A parallel-group feasibility randomised controlled trial design with a 1:1 allocation ratio to 1) i-REBOUND programme receiving physical exercise and support for sustained engagement in physical activity through behavioural change techniques, or 2) behavioural change techniques for physical activity. Both interventions will proceed for six months and be delivered digitally through a mobile app. The feasibility outcomes (i.e., reach, adherence, safety and fidelity) will be monitored throughout the study. Acceptability will be assessed using the Telehealth Usability Questionnaire and further explored through qualitative interviews with a subset of both study participants and the physiotherapists delivering the intervention. Clinical outcomes on preliminary effects of the intervention will include blood pressure, engagement in physical activity, self-perceived exercise self-efficacy, fatigue, depression, anxiety, stress and health-related quality of life and will be measured at baseline and at 3, 6 and 12 months after the baseline assessments. DISCUSSION: We hypothesise that the mHealth delivery of the i-REBOUND programme will be feasible and acceptable in people post stroke/TIA living in rural and urban regions of Sweden. The results of this feasibility trial will inform the development of full-scale and appropriately powered trial to test the effects and costs of mHealth delivered physical activity for people after stroke or TIA. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT05111951. Registered November 8, 2021. |
format | Online Article Text |
id | pubmed-10043533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100435332023-03-28 Mobile health to promote physical activity in people post stroke or transient ischemic attack – study protocol for a feasibility randomised controlled trial Thurston, Charlotte Bezuidenhout, Lucian Humphries, Sophia Johansson, Sverker von Koch, Lena Häger, Charlotte K. Holmlund, Lisa Sundberg, Carl Johan Garcia-Ptacek, Sara Kwak, Lydia Nilsson, Michael English, Coralie Conradsson, David Moulaee BMC Neurol Study Protocol BACKGROUND: Physical activity is essential to improve health and reduce the risk of recurrence of stroke or transient ischemic attack (TIA). Still, people post stroke or TIA are often physically inactive and the availability of physical activity promotion services are often limited. This study builds on an existing Australian telehealth-delivered programme (i-REBOUND– Let’s get moving) which provides support for home-based physical activity for people post stroke or TIA. The aim of this study is to test the feasibility, acceptability, and preliminary effects of a mobile Health (mHealth) version of the i-REBOUND programme for the promotion of physical activity in people post stroke or TIA living in Sweden. METHODS: One hundred and twenty participants with stroke or TIA will be recruited via advertisement. A parallel-group feasibility randomised controlled trial design with a 1:1 allocation ratio to 1) i-REBOUND programme receiving physical exercise and support for sustained engagement in physical activity through behavioural change techniques, or 2) behavioural change techniques for physical activity. Both interventions will proceed for six months and be delivered digitally through a mobile app. The feasibility outcomes (i.e., reach, adherence, safety and fidelity) will be monitored throughout the study. Acceptability will be assessed using the Telehealth Usability Questionnaire and further explored through qualitative interviews with a subset of both study participants and the physiotherapists delivering the intervention. Clinical outcomes on preliminary effects of the intervention will include blood pressure, engagement in physical activity, self-perceived exercise self-efficacy, fatigue, depression, anxiety, stress and health-related quality of life and will be measured at baseline and at 3, 6 and 12 months after the baseline assessments. DISCUSSION: We hypothesise that the mHealth delivery of the i-REBOUND programme will be feasible and acceptable in people post stroke/TIA living in rural and urban regions of Sweden. The results of this feasibility trial will inform the development of full-scale and appropriately powered trial to test the effects and costs of mHealth delivered physical activity for people after stroke or TIA. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT05111951. Registered November 8, 2021. BioMed Central 2023-03-28 /pmc/articles/PMC10043533/ /pubmed/36978045 http://dx.doi.org/10.1186/s12883-023-03163-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Study Protocol Thurston, Charlotte Bezuidenhout, Lucian Humphries, Sophia Johansson, Sverker von Koch, Lena Häger, Charlotte K. Holmlund, Lisa Sundberg, Carl Johan Garcia-Ptacek, Sara Kwak, Lydia Nilsson, Michael English, Coralie Conradsson, David Moulaee Mobile health to promote physical activity in people post stroke or transient ischemic attack – study protocol for a feasibility randomised controlled trial |
title | Mobile health to promote physical activity in people post stroke or transient ischemic attack – study protocol for a feasibility randomised controlled trial |
title_full | Mobile health to promote physical activity in people post stroke or transient ischemic attack – study protocol for a feasibility randomised controlled trial |
title_fullStr | Mobile health to promote physical activity in people post stroke or transient ischemic attack – study protocol for a feasibility randomised controlled trial |
title_full_unstemmed | Mobile health to promote physical activity in people post stroke or transient ischemic attack – study protocol for a feasibility randomised controlled trial |
title_short | Mobile health to promote physical activity in people post stroke or transient ischemic attack – study protocol for a feasibility randomised controlled trial |
title_sort | mobile health to promote physical activity in people post stroke or transient ischemic attack – study protocol for a feasibility randomised controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043533/ https://www.ncbi.nlm.nih.gov/pubmed/36978045 http://dx.doi.org/10.1186/s12883-023-03163-0 |
work_keys_str_mv | AT thurstoncharlotte mobilehealthtopromotephysicalactivityinpeoplepoststrokeortransientischemicattackstudyprotocolforafeasibilityrandomisedcontrolledtrial AT bezuidenhoutlucian mobilehealthtopromotephysicalactivityinpeoplepoststrokeortransientischemicattackstudyprotocolforafeasibilityrandomisedcontrolledtrial AT humphriessophia mobilehealthtopromotephysicalactivityinpeoplepoststrokeortransientischemicattackstudyprotocolforafeasibilityrandomisedcontrolledtrial AT johanssonsverker mobilehealthtopromotephysicalactivityinpeoplepoststrokeortransientischemicattackstudyprotocolforafeasibilityrandomisedcontrolledtrial AT vonkochlena mobilehealthtopromotephysicalactivityinpeoplepoststrokeortransientischemicattackstudyprotocolforafeasibilityrandomisedcontrolledtrial AT hagercharlottek mobilehealthtopromotephysicalactivityinpeoplepoststrokeortransientischemicattackstudyprotocolforafeasibilityrandomisedcontrolledtrial AT holmlundlisa mobilehealthtopromotephysicalactivityinpeoplepoststrokeortransientischemicattackstudyprotocolforafeasibilityrandomisedcontrolledtrial AT sundbergcarljohan mobilehealthtopromotephysicalactivityinpeoplepoststrokeortransientischemicattackstudyprotocolforafeasibilityrandomisedcontrolledtrial AT garciaptaceksara mobilehealthtopromotephysicalactivityinpeoplepoststrokeortransientischemicattackstudyprotocolforafeasibilityrandomisedcontrolledtrial AT kwaklydia mobilehealthtopromotephysicalactivityinpeoplepoststrokeortransientischemicattackstudyprotocolforafeasibilityrandomisedcontrolledtrial AT nilssonmichael mobilehealthtopromotephysicalactivityinpeoplepoststrokeortransientischemicattackstudyprotocolforafeasibilityrandomisedcontrolledtrial AT englishcoralie mobilehealthtopromotephysicalactivityinpeoplepoststrokeortransientischemicattackstudyprotocolforafeasibilityrandomisedcontrolledtrial AT conradssondavidmoulaee mobilehealthtopromotephysicalactivityinpeoplepoststrokeortransientischemicattackstudyprotocolforafeasibilityrandomisedcontrolledtrial |