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WFRF:(Tseli Elena)
 

Sökning: WFRF:(Tseli Elena) > Effectiveness of th...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004150naa a2200361 4500
001oai:DiVA.org:du-41423
003SwePub
008220511s2022 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:du-414232 URI
040 a (SwePub)du
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a kon2 swepub-publicationtype
100a Sjöberg, Veronicau Högskolan Dalarna,Vårdvetenskap,Medicinsk vetenskap,DU/Pain4 aut0 (Swepub:du)vsj
2451 0a Effectiveness of the eVISualisation of physical activity and pain (eVIS) intervention in Interdisciplinary Pain Rehabilitation Programs :b Study Protocol for a Registry-based Randomised Controlled Clinical Trial
264 1c 2022
338 a print2 rdacarrier
520 a Background and aims: * Interdisciplinary Pain Rehabilitation Programs (IPRPs) are considered to be superior to single-treatment measures in chronic pain treatment. However, the effects of IPRPs are moderate and as many as 30% of patients deteriorate in some outcomes. Although physical activity and exercise are central components in IPRPs, many patients struggle to achieve and maintain the recommended levels. An intervention, entitled eVISualisation of physical activity and pain (eVIS), has now been systematically developed and designed to facilitate patients with chronic pain in achieving and maintaining recommended physical activity levels. The aim of the present study protocol is to transparently report on the methodology, outcomes, and processes for an initiated registry-based randomized controlled trial (R-RCT), which will evaluate the effectiveness of eVIS on the primary outcome physical health and defined secondary outcomes. Methods: * Participants (approximately 400) will be recruited from IPRP units and randomly allocated to either IPRP with an addition of eVIS or to treatment as usual by IPRP. eVIS entails objectively measured physical activity and patient-reported outcomes of pain intensity, effect on daily activities and pharmaceutical consumption. Data is collected and visualized in a web application, PATRON. Pilot analyses evaluating the feasibility of the R-RCT will be performed on data from initial 30 participants. Outcomes will be extracted from PATRON and from six national registries. Multivariate statistics and repeated measures analyses will be performed. Results: * Recruitment will be initiated in late 2021. ClinicalTrials.gov identifier: NCT05009459. Conclusions: * This study protocol describes a R-RCT that is designed to provide robust data on the feasibility and effectiveness of eVIS as an addition to IPRPs.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Hälsovetenskapx Sjukgymnastik0 (SwePub)303072 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Health Sciencesx Physiotherapy0 (SwePub)303072 hsv//eng
700a Tseli, Elenau Högskolan Dalarna,Medicinsk vetenskap,Du/Pain4 aut0 (Swepub:du)ezt
700a Monnier, Andreasu Högskolan Dalarna,Medicinsk vetenskap,Military Academy Karlberg, Swedish Armed Forces,Du/Pain4 aut0 (Swepub:du)anmo
700a Westergren, Jensu Högskolan Dalarna,Idrotts- och hälsovetenskap,Du/Pain4 aut0 (Swepub:du)jws
700a LoMartire, Riccardou Department of Research and Higher Education, Region Dalarna,DU/Pain4 aut
700a Äng, Björnu Högskolan Dalarna,Medicinsk vetenskap,Department of Research and Higher Education, Region Dalarna,DU/Pain4 aut0 (Swepub:du)bja
700a Hagströmer, Mariau Department of Neurobiology, Care Sciences and Society, Karolinska Institutet and Academic Primary Health Care Centre, Region Stockholm4 aut
700a Björk, Mathildau Department for Prevention, Rehabilitation and Community Medicine, Linköping University,DU/Pain4 aut
700a Vixner, Lindau Högskolan Dalarna,Medicinsk vetenskap,DU/Pain4 aut0 (Swepub:du)lvi
710a Högskolan Dalarnab Vårdvetenskap4 org
856u https://efic-congress.org/
856u https://du.diva-portal.org/smash/get/diva2:1657606/ATTACHMENT01.pdfy attachment:print
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:du-41423

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