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Physical Activity Together for Multiple Sclerosis (PAT-MS): A randomized controlled feasibility trial of a dyadic behaviour change intervention

BACKGROUND: Many people with advanced multiple sclerosis (MS) and their care-partners do not engage in sufficient physical activity (PA) for health benefits. We developed “Physical Activity Together for MS (PAT-MS)”, a 12-week dyadic behavioural intervention, to promote PA among these dyads. Herein,...

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Autores principales: Fakolade, Afolasade, Awadia, Zain, Cardwell, Katherine, McKenna, Odessa, Venasse, Myriam, Hume, Taylor, Ludgate, Julia, Freedman, Mark S., Finlayson, Marcia, Latimer-Cheung, Amy E., Pilutti, Lara A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10622616/
https://www.ncbi.nlm.nih.gov/pubmed/37928934
http://dx.doi.org/10.1016/j.conctc.2023.101222
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author Fakolade, Afolasade
Awadia, Zain
Cardwell, Katherine
McKenna, Odessa
Venasse, Myriam
Hume, Taylor
Ludgate, Julia
Freedman, Mark S.
Finlayson, Marcia
Latimer-Cheung, Amy E.
Pilutti, Lara A.
author_facet Fakolade, Afolasade
Awadia, Zain
Cardwell, Katherine
McKenna, Odessa
Venasse, Myriam
Hume, Taylor
Ludgate, Julia
Freedman, Mark S.
Finlayson, Marcia
Latimer-Cheung, Amy E.
Pilutti, Lara A.
author_sort Fakolade, Afolasade
collection PubMed
description BACKGROUND: Many people with advanced multiple sclerosis (MS) and their care-partners do not engage in sufficient physical activity (PA) for health benefits. We developed “Physical Activity Together for MS (PAT-MS)”, a 12-week dyadic behavioural intervention, to promote PA among these dyads. Herein, we evaluated the feasibility of PAT-MS before a definitive trial. METHODS: A randomized controlled feasibility trial, with 1:1 allocation into the intervention or wait-list control condition. Predefined progression criteria included rates of recruitment, retention, safety, participant satisfaction and adherence. Changes in self-reported and accelerometer-measured PA were assessed at baseline and post-intervention using mixed-factor ANOVAs. Effects sizes were calculated as Cohen's d. RESULTS: The recruitment rate (i.e., 20 participants in 10 months) was not acceptable. However, retention (80%) was acceptable. No serious adverse events were reported. There were high levels of participant satisfaction with the intervention (content (median = 6 out of 7), facilitator (median = 7 out of 7), and delivery (median = 5 out of 7)) and adherence (92% of the group sessions, 83% of the individual support calls, and 80% of the practice activities were completed). There were statistically significant time-by-condition interactions on self-reported PA, steps/day, and %wear time and minutes in sedentary behaviour, and moderate-to-vigorous PA from baseline to post-intervention in people with MS and their family care-partners. CONCLUSION: PAT-MS appears feasible, safe, and efficacious for PA promotion in MS dyads. We established effect size estimates to power a future definitive trial and identified necessary methodological changes to increase the efficiency of study procedures and improve the quality of the intervention. TRIAL REGISTRATION: ClinicalTrials.gov NCT04267185; Registered February 12, 2020, https://clinicaltrials.gov/ct2/show/NCT04267185.
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spelling pubmed-106226162023-11-04 Physical Activity Together for Multiple Sclerosis (PAT-MS): A randomized controlled feasibility trial of a dyadic behaviour change intervention Fakolade, Afolasade Awadia, Zain Cardwell, Katherine McKenna, Odessa Venasse, Myriam Hume, Taylor Ludgate, Julia Freedman, Mark S. Finlayson, Marcia Latimer-Cheung, Amy E. Pilutti, Lara A. Contemp Clin Trials Commun Article BACKGROUND: Many people with advanced multiple sclerosis (MS) and their care-partners do not engage in sufficient physical activity (PA) for health benefits. We developed “Physical Activity Together for MS (PAT-MS)”, a 12-week dyadic behavioural intervention, to promote PA among these dyads. Herein, we evaluated the feasibility of PAT-MS before a definitive trial. METHODS: A randomized controlled feasibility trial, with 1:1 allocation into the intervention or wait-list control condition. Predefined progression criteria included rates of recruitment, retention, safety, participant satisfaction and adherence. Changes in self-reported and accelerometer-measured PA were assessed at baseline and post-intervention using mixed-factor ANOVAs. Effects sizes were calculated as Cohen's d. RESULTS: The recruitment rate (i.e., 20 participants in 10 months) was not acceptable. However, retention (80%) was acceptable. No serious adverse events were reported. There were high levels of participant satisfaction with the intervention (content (median = 6 out of 7), facilitator (median = 7 out of 7), and delivery (median = 5 out of 7)) and adherence (92% of the group sessions, 83% of the individual support calls, and 80% of the practice activities were completed). There were statistically significant time-by-condition interactions on self-reported PA, steps/day, and %wear time and minutes in sedentary behaviour, and moderate-to-vigorous PA from baseline to post-intervention in people with MS and their family care-partners. CONCLUSION: PAT-MS appears feasible, safe, and efficacious for PA promotion in MS dyads. We established effect size estimates to power a future definitive trial and identified necessary methodological changes to increase the efficiency of study procedures and improve the quality of the intervention. TRIAL REGISTRATION: ClinicalTrials.gov NCT04267185; Registered February 12, 2020, https://clinicaltrials.gov/ct2/show/NCT04267185. Elsevier 2023-10-16 /pmc/articles/PMC10622616/ /pubmed/37928934 http://dx.doi.org/10.1016/j.conctc.2023.101222 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Fakolade, Afolasade
Awadia, Zain
Cardwell, Katherine
McKenna, Odessa
Venasse, Myriam
Hume, Taylor
Ludgate, Julia
Freedman, Mark S.
Finlayson, Marcia
Latimer-Cheung, Amy E.
Pilutti, Lara A.
Physical Activity Together for Multiple Sclerosis (PAT-MS): A randomized controlled feasibility trial of a dyadic behaviour change intervention
title Physical Activity Together for Multiple Sclerosis (PAT-MS): A randomized controlled feasibility trial of a dyadic behaviour change intervention
title_full Physical Activity Together for Multiple Sclerosis (PAT-MS): A randomized controlled feasibility trial of a dyadic behaviour change intervention
title_fullStr Physical Activity Together for Multiple Sclerosis (PAT-MS): A randomized controlled feasibility trial of a dyadic behaviour change intervention
title_full_unstemmed Physical Activity Together for Multiple Sclerosis (PAT-MS): A randomized controlled feasibility trial of a dyadic behaviour change intervention
title_short Physical Activity Together for Multiple Sclerosis (PAT-MS): A randomized controlled feasibility trial of a dyadic behaviour change intervention
title_sort physical activity together for multiple sclerosis (pat-ms): a randomized controlled feasibility trial of a dyadic behaviour change intervention
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10622616/
https://www.ncbi.nlm.nih.gov/pubmed/37928934
http://dx.doi.org/10.1016/j.conctc.2023.101222
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