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Content Validity and Feasibility of the eVISualisation of physical activity and pain (eVIS) intervention in Interdisciplinary Pain Rehabilitation Programs: Valuable steps in a systematical development and evaluation process
Dalarna University, School of Health and Welfare, Care Sciences. Dalarna University, School of Health and Welfare, Medical Science. (DU/Pain)ORCID iD: 0000-0002-3843-0407
Dalarna University, School of Health and Welfare, Medical Science. (DU/Pain)ORCID iD: 0000-0002-8307-259x
Department for Prevention, Rehabilitation, and Community Medicine, Linköping University. (DU/Pain)ORCID iD: 0000-0002-1607-187X
Dalarna University, School of Health and Welfare, Medical Science. Department of Neurobiology, Care Sciences and Society, Division of Physiotherapy, Karolinska Institutet; Department for Research and Higher Education, Center for Clinical Research Dalarna, Uppsala University, Region Dalarna. (DU/Pain)ORCID iD: 0000-0001-7767-4589
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2022 (English)Conference paper, Poster (with or without abstract) (Refereed)
Abstract [en]

Background and aims: *Low physical health is one consequence that chronic pain encompasses. To improveeffectiveness of Interdisciplinary pain rehabilitation programs (IPRP) theeVISualisation of physical activity and pain (eVIS) intervention was developed. Thepurpose of this study was to evaluate eVIS validity by the aspects of content validityand clinical feasibility in IPRP-context.Methods: *This observational study was performed in 3 phases. Twenty-two field experts (patients,caregivers, researchers) participated, and provided quantitative scores and qualitativecomments on eVIS and its included elements (data collection, visualization,communication). In phase 1, ratings on a four-point Likert scale of each element´scontent validity (relevance, simplicity, safety) were collected through digitalquestionnaires. Three iterative assessment loops were completed, each followed byconsensus panel protocol revisions. Item-level content validity index (I-CVI), averageand overall CVI were calculated, and free-text comments were analyzed. In phase 2,ratings of content validity and elements’ clinical feasibility categorized in 5 focus areas(acceptability, demand, implementation, limited efficacy, practicality), were collectedfrom patients and caregivers after 2-3 weeks test trial. Phase 3 involved follow-up focusgroup interview with caregivers on specific ratings, as well as interviews with expertsin clinical pain management pharmacology.Results: *CVI for relevance, simplicity and safety improved over time and were all rated abovecut-off (0.78). Revisions were mainly made in the visualization element. In phase 2,participants rated eVIS as relevant and feasible to use in clinical IPRP-context.Conclusions: *Patients, caregivers, and researchers found eVIS valid in IPRP-context. Methodicalvalidation was essential to ascertain eVIS’ substantiality before clinical trial.

Place, publisher, year, edition, pages
2022.
National Category
Physiotherapy
Identifiers
URN: urn:nbn:se:du-41424OAI: oai:DiVA.org:du-41424DiVA, id: diva2:1657613
Conference
12th Congress of the European Pain Federation EFIC, Dublin, Ireland, 27-30 April 2022
Available from: 2022-05-11 Created: 2022-05-11 Last updated: 2025-03-12Bibliographically approved

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Sjöberg, VeronicaTseli, ElenaÄng, BjörnVixner, Linda

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CiteExportLink to record
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Citation style
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