28 Mobile health biometrics to prescribe immediate remote physical activity for enhancing uptake to cardiac rehabilitation (MOTIVATE-CR+): protocol for a randomised controlled feasibility trial
BackgroundCardiac Rehabilitation (CR) can reduce cardiovascular mortality and improve health related quality of life. In the United Kingdom patient uptake of CR remains low (52%), falling well short of the target in the 2019 NHS Long-term plan (85%). Mobile health (mHealth) technologies, offering bi...
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description | BackgroundCardiac Rehabilitation (CR) can reduce cardiovascular mortality and improve health related quality of life. In the United Kingdom patient uptake of CR remains low (52%), falling well short of the target in the 2019 NHS Long-term plan (85%). Mobile health (mHealth) technologies, offering biometric data to patients and healthcare professionals, may bridge the gap between patient discharge from hospital and in-person supervised exercise and physical activity (PA) advice. Early intervention could lead to improved CR uptake and enable patients to engage in regular long-term physically active lifestyles quicker.AimThis randomised controlled trial (RCT) will evaluate the feasibility of mHealth technology when incorporated into a structured home-based walking intervention, in people with recent myocardial infarction.MethodsThis is a feasibility, assessor blinded, parallel group RCT. Participants will be allocated to either CR standard care (control group) or CR standard care + mHealth supported exercise counselling (mHealth group) (figure 1). The trial was approved in the UK by the Northwest – Greater Manchester East Research Ethics Committee (22/NW/0301) and is registered on ClinicalTrials.gov: NCT05774587. Feasibility outcomes include; the number of patients approached, screened and eligible; the percentage of patients that decline CR (including reasons), agree to CR and consent to being part of the study; the percentage of patients that enroll in standard CR and reasons for drop out; and the percentage of participants that complete clinical, physical and psychosocial outcomes to identify a suitable primary outcome for a future definitive trial. Device derived data will be downloaded using manufacturers’ software and processed in R (R Core Team,Vienna, Austria) using the open-source GGIR software package (http://cran.r-project.org). Qualitative data will be thematically analyzed and coded using NVivo V.12TM software.Abstract 28 Figure 1Schematic of the experimental design. Abbreviations: CR; cardiac rehabilitation, n; number, CS; counselling session[Figure omitted. See PDF]Strengths and limitationsThe MOTIVATE-CR+ intervention may increase the uptake of CR by supporting patients to become physically active between discharge and the start of supervised CR and allowing patients that recently experienced a myocardial infarction to co-design a personalized and progressive walking programme with the support of a clinical exercise physiologist. The intervent |
doi_str_mv | 10.1136/heartjnl-2023-BACPR.24 |
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In the United Kingdom patient uptake of CR remains low (52%), falling well short of the target in the 2019 NHS Long-term plan (85%). Mobile health (mHealth) technologies, offering biometric data to patients and healthcare professionals, may bridge the gap between patient discharge from hospital and in-person supervised exercise and physical activity (PA) advice. Early intervention could lead to improved CR uptake and enable patients to engage in regular long-term physically active lifestyles quicker.AimThis randomised controlled trial (RCT) will evaluate the feasibility of mHealth technology when incorporated into a structured home-based walking intervention, in people with recent myocardial infarction.MethodsThis is a feasibility, assessor blinded, parallel group RCT. Participants will be allocated to either CR standard care (control group) or CR standard care + mHealth supported exercise counselling (mHealth group) (figure 1). The trial was approved in the UK by the Northwest – Greater Manchester East Research Ethics Committee (22/NW/0301) and is registered on ClinicalTrials.gov: NCT05774587. Feasibility outcomes include; the number of patients approached, screened and eligible; the percentage of patients that decline CR (including reasons), agree to CR and consent to being part of the study; the percentage of patients that enroll in standard CR and reasons for drop out; and the percentage of participants that complete clinical, physical and psychosocial outcomes to identify a suitable primary outcome for a future definitive trial. Device derived data will be downloaded using manufacturers’ software and processed in R (R Core Team,Vienna, Austria) using the open-source GGIR software package (http://cran.r-project.org). Qualitative data will be thematically analyzed and coded using NVivo V.12TM software.Abstract 28 Figure 1Schematic of the experimental design. Abbreviations: CR; cardiac rehabilitation, n; number, CS; counselling session[Figure omitted. See PDF]Strengths and limitationsThe MOTIVATE-CR+ intervention may increase the uptake of CR by supporting patients to become physically active between discharge and the start of supervised CR and allowing patients that recently experienced a myocardial infarction to co-design a personalized and progressive walking programme with the support of a clinical exercise physiologist. The intervention also enables participants to communicate regularly with a clinical exercise physiologist and gain feedback on the exercise sessions they complete. The intervention is not, however, embedded within the current cardiac rehabilitation landscape, as such, future work will be needed to address how the intervention could fit within service structures.</description><identifier>ISSN: 1355-6037</identifier><identifier>EISSN: 1468-201X</identifier><identifier>DOI: 10.1136/heartjnl-2023-BACPR.24</identifier><language>eng</language><publisher>London: BMJ Publishing Group LTD</publisher><subject>Cardiovascular disease ; Exercise ; Heart attacks ; Patients ; Physical fitness ; Rehabilitation ; Software ; Telemedicine</subject><ispartof>Heart (British Cardiac Society), 2023-10, Vol.109 (Suppl 5), p.A14-A15</ispartof><rights>2023 Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Crozier, Anthony</creatorcontrib><creatorcontrib>Cocks, Matthew</creatorcontrib><creatorcontrib>Hesketh, Katie</creatorcontrib><creatorcontrib>Miller, Gemma</creatorcontrib><creatorcontrib>McGregor, Gordon</creatorcontrib><creatorcontrib>Thomas, Laura</creatorcontrib><creatorcontrib>Jones, Helen</creatorcontrib><title>28 Mobile health biometrics to prescribe immediate remote physical activity for enhancing uptake to cardiac rehabilitation (MOTIVATE-CR+): protocol for a randomised controlled feasibility trial</title><title>Heart (British Cardiac Society)</title><description>BackgroundCardiac Rehabilitation (CR) can reduce cardiovascular mortality and improve health related quality of life. In the United Kingdom patient uptake of CR remains low (52%), falling well short of the target in the 2019 NHS Long-term plan (85%). Mobile health (mHealth) technologies, offering biometric data to patients and healthcare professionals, may bridge the gap between patient discharge from hospital and in-person supervised exercise and physical activity (PA) advice. Early intervention could lead to improved CR uptake and enable patients to engage in regular long-term physically active lifestyles quicker.AimThis randomised controlled trial (RCT) will evaluate the feasibility of mHealth technology when incorporated into a structured home-based walking intervention, in people with recent myocardial infarction.MethodsThis is a feasibility, assessor blinded, parallel group RCT. Participants will be allocated to either CR standard care (control group) or CR standard care + mHealth supported exercise counselling (mHealth group) (figure 1). The trial was approved in the UK by the Northwest – Greater Manchester East Research Ethics Committee (22/NW/0301) and is registered on ClinicalTrials.gov: NCT05774587. Feasibility outcomes include; the number of patients approached, screened and eligible; the percentage of patients that decline CR (including reasons), agree to CR and consent to being part of the study; the percentage of patients that enroll in standard CR and reasons for drop out; and the percentage of participants that complete clinical, physical and psychosocial outcomes to identify a suitable primary outcome for a future definitive trial. Device derived data will be downloaded using manufacturers’ software and processed in R (R Core Team,Vienna, Austria) using the open-source GGIR software package (http://cran.r-project.org). Qualitative data will be thematically analyzed and coded using NVivo V.12TM software.Abstract 28 Figure 1Schematic of the experimental design. Abbreviations: CR; cardiac rehabilitation, n; number, CS; counselling session[Figure omitted. See PDF]Strengths and limitationsThe MOTIVATE-CR+ intervention may increase the uptake of CR by supporting patients to become physically active between discharge and the start of supervised CR and allowing patients that recently experienced a myocardial infarction to co-design a personalized and progressive walking programme with the support of a clinical exercise physiologist. The intervention also enables participants to communicate regularly with a clinical exercise physiologist and gain feedback on the exercise sessions they complete. The intervention is not, however, embedded within the current cardiac rehabilitation landscape, as such, future work will be needed to address how the intervention could fit within service structures.</description><subject>Cardiovascular disease</subject><subject>Exercise</subject><subject>Heart attacks</subject><subject>Patients</subject><subject>Physical fitness</subject><subject>Rehabilitation</subject><subject>Software</subject><subject>Telemedicine</subject><issn>1355-6037</issn><issn>1468-201X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNotkM1KxDAUhYsoqKOvIAE3ilTTJE077sbiH4woMog7uU1vbca0GZOMMDs3Pplv4pMYf1bncOF853CTZC-jx1nG5UmH4MJ8MCmjjKdnk-ru_piJtWQrE7KMx-xxPXqe56mkvNhMtr2fU0rFuJRbyScrv94_bmytDZJIMqEjtbY9BqeVJ8GShUOvnK6R6L7HRkNA4rC3URbdymsFhoAK-k2HFWmtIzh0MCg9PJPlIsAL_kAUuJhUMdhBrNIBgrYDObi5nV0_TGbnaXV_dHgau2ywyppfDhAHQ2N77bEhyg7BWWOibRG8_oWsSFwJZifZaMF43P3XUTK7OJ9VV-n09vK6mkzTRSFF2oAqkQkuKW2oVFhmosaiyBtWtpRjwYDlpchrmY95HT-JUCOgyFkhgNG25qNk_w8bV74u0YenuV26ITY-sbLgjMssL_g3Ofl_Ig</recordid><startdate>20231001</startdate><enddate>20231001</enddate><creator>Crozier, Anthony</creator><creator>Cocks, Matthew</creator><creator>Hesketh, Katie</creator><creator>Miller, Gemma</creator><creator>McGregor, Gordon</creator><creator>Thomas, Laura</creator><creator>Jones, Helen</creator><general>BMJ Publishing Group LTD</general><scope>K9.</scope></search><sort><creationdate>20231001</creationdate><title>28 Mobile health biometrics to prescribe immediate remote physical activity for enhancing uptake to cardiac rehabilitation (MOTIVATE-CR+): protocol for a randomised controlled feasibility trial</title><author>Crozier, Anthony ; Cocks, Matthew ; Hesketh, Katie ; Miller, Gemma ; McGregor, Gordon ; Thomas, Laura ; Jones, Helen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p764-dac8e243600d06ce814be775d28f03e72a25845b6593b023eabeae45274a20fb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Cardiovascular disease</topic><topic>Exercise</topic><topic>Heart attacks</topic><topic>Patients</topic><topic>Physical fitness</topic><topic>Rehabilitation</topic><topic>Software</topic><topic>Telemedicine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Crozier, Anthony</creatorcontrib><creatorcontrib>Cocks, Matthew</creatorcontrib><creatorcontrib>Hesketh, Katie</creatorcontrib><creatorcontrib>Miller, Gemma</creatorcontrib><creatorcontrib>McGregor, Gordon</creatorcontrib><creatorcontrib>Thomas, Laura</creatorcontrib><creatorcontrib>Jones, Helen</creatorcontrib><collection>ProQuest Health & Medical Complete (Alumni)</collection><jtitle>Heart (British Cardiac Society)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Crozier, Anthony</au><au>Cocks, Matthew</au><au>Hesketh, Katie</au><au>Miller, Gemma</au><au>McGregor, Gordon</au><au>Thomas, Laura</au><au>Jones, Helen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>28 Mobile health biometrics to prescribe immediate remote physical activity for enhancing uptake to cardiac rehabilitation (MOTIVATE-CR+): protocol for a randomised controlled feasibility trial</atitle><jtitle>Heart (British Cardiac Society)</jtitle><date>2023-10-01</date><risdate>2023</risdate><volume>109</volume><issue>Suppl 5</issue><spage>A14</spage><epage>A15</epage><pages>A14-A15</pages><issn>1355-6037</issn><eissn>1468-201X</eissn><abstract>BackgroundCardiac Rehabilitation (CR) can reduce cardiovascular mortality and improve health related quality of life. In the United Kingdom patient uptake of CR remains low (52%), falling well short of the target in the 2019 NHS Long-term plan (85%). Mobile health (mHealth) technologies, offering biometric data to patients and healthcare professionals, may bridge the gap between patient discharge from hospital and in-person supervised exercise and physical activity (PA) advice. Early intervention could lead to improved CR uptake and enable patients to engage in regular long-term physically active lifestyles quicker.AimThis randomised controlled trial (RCT) will evaluate the feasibility of mHealth technology when incorporated into a structured home-based walking intervention, in people with recent myocardial infarction.MethodsThis is a feasibility, assessor blinded, parallel group RCT. Participants will be allocated to either CR standard care (control group) or CR standard care + mHealth supported exercise counselling (mHealth group) (figure 1). The trial was approved in the UK by the Northwest – Greater Manchester East Research Ethics Committee (22/NW/0301) and is registered on ClinicalTrials.gov: NCT05774587. Feasibility outcomes include; the number of patients approached, screened and eligible; the percentage of patients that decline CR (including reasons), agree to CR and consent to being part of the study; the percentage of patients that enroll in standard CR and reasons for drop out; and the percentage of participants that complete clinical, physical and psychosocial outcomes to identify a suitable primary outcome for a future definitive trial. Device derived data will be downloaded using manufacturers’ software and processed in R (R Core Team,Vienna, Austria) using the open-source GGIR software package (http://cran.r-project.org). Qualitative data will be thematically analyzed and coded using NVivo V.12TM software.Abstract 28 Figure 1Schematic of the experimental design. Abbreviations: CR; cardiac rehabilitation, n; number, CS; counselling session[Figure omitted. See PDF]Strengths and limitationsThe MOTIVATE-CR+ intervention may increase the uptake of CR by supporting patients to become physically active between discharge and the start of supervised CR and allowing patients that recently experienced a myocardial infarction to co-design a personalized and progressive walking programme with the support of a clinical exercise physiologist. The intervention also enables participants to communicate regularly with a clinical exercise physiologist and gain feedback on the exercise sessions they complete. The intervention is not, however, embedded within the current cardiac rehabilitation landscape, as such, future work will be needed to address how the intervention could fit within service structures.</abstract><cop>London</cop><pub>BMJ Publishing Group LTD</pub><doi>10.1136/heartjnl-2023-BACPR.24</doi><oa>free_for_read</oa></addata></record> |
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title | 28 Mobile health biometrics to prescribe immediate remote physical activity for enhancing uptake to cardiac rehabilitation (MOTIVATE-CR+): protocol for a randomised controlled feasibility trial |
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