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Publications (10 of 37) Show all publications
Leijon, A., Nilsson, T., Sillén, U., Hellström, A.-L., Vixner, L. & Hedin Skogman, B. (2024). Content validity and feasibility of the BABITT questionnaire: assisted infant toilet training and bowel and bladder function in children. In: : . Paper presented at OMEP European Conference and Assembly 2024, Sustainability from the Start, hosted by Kristianstad University and OMEP Sweden, Kristianstad April 24-26 2024.
Open this publication in new window or tab >>Content validity and feasibility of the BABITT questionnaire: assisted infant toilet training and bowel and bladder function in children
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2024 (English)Conference paper, Oral presentation with published abstract (Other academic)
Abstract [en]

Background: Functional bowel and bladder disorders are prevalent among children. The impact of assisted infant toilet training on the prevalence of childhood bowel and bladder disorders has not previously been investigated. As self-reported bowel and bladder symptoms can be unreliable, robust tools are essential to evaluate interventions. The ROME Foundation offers diagnostic criteria for functional gastrointestinal disorders, while the International Children's Continence Society (ICCS) provides definitions for functional bladder disorders. Our research group has launched the BABITT study, a two-armed intervention study to investigate whether assisted infant toilet training reduces the prevalence of functional bowel and bladder disorders.

Aim: To construct a questionnaire, assessing bowel and bladder function in children introduced to infant toilet training and to evaluate content validity as well as feasibility.

Methods: In three consecutive steps, a web-based questionnaire was developed. In Step 1, the questionnaire was outlined based on literature review and consensus panel discussions. In Step 2, the questionnaire was validated regarding relevance and simplicity by the content validity index (CVI) method. In Step 3, a pilot phase allowed for assessment of feasibility in the clinical study setting.

Results: In Step 1, the Rome criteria and ICCS frameworks were selected for primary outcomes. After the final assessment round in Step 2, the i-CVI ranged from 0.88-1.00 in most items, in all domains, for both relevance and simplicity. Generally lower scores on simplicity emphasized revisions of this aspect of the items. In the pilot phase Step 3, respondent burden was analysed and feasibility assessed. The response rate at the 2-months questionnaire was 95% and acceptability of the intervention was satisfactory.

Conclusion: A web- based questionnaire for assessment of parent-reported bladder and bowel function in children who are introduced to infant toilet training was developed. The questionnaire emerged as valid and feasible in its context.

National Category
Pediatrics
Identifiers
urn:nbn:se:du-48654 (URN)
Conference
OMEP European Conference and Assembly 2024, Sustainability from the Start, hosted by Kristianstad University and OMEP Sweden, Kristianstad April 24-26 2024
Available from: 2024-06-04 Created: 2024-06-04 Last updated: 2024-06-04
Sjöberg, V., Monnier, A., Tseli, E., Lo Martire, R., Hagströmer, M., Björk, M., . . . Vixner, L. (2024). Feasibility and acceptability of design and conduct of a registry-based randomised clinical trial evaluating eVIS as a digital support for physical activity in interdisciplinary pain rehabilitation programs: A randomised pilot study. Digital Health, 10
Open this publication in new window or tab >>Feasibility and acceptability of design and conduct of a registry-based randomised clinical trial evaluating eVIS as a digital support for physical activity in interdisciplinary pain rehabilitation programs: A randomised pilot study
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2024 (English)In: Digital Health, ISSN 2055-2076, Vol. 10Article in journal (Refereed) Published
Abstract [en]

Background

Patients with chronic pain often struggle to engage in physical activity despite its health benefits. The eVISualisation of physical activity and pain intervention (eVIS) was developed to support adherence to physical activity plans in Interdisciplinary Pain Rehabilitation Programs (IPRPs) by visualising activity, pain levels, pain interference, and pharmacological use. This pilot study assesses the feasibility and acceptability of trial design and trial conduct of a registry-based randomised clinical trial (R-RCT).

Method

This randomised clinical pilot study included the first 10% (n = 39, mean age 43.5, 74.4% females) of the R-RCT sample (n≈400). Participants with non-cancer chronic pain from six IPRP units were randomly assigned to either the intervention group (IPRP + eVIS, n = 19) or the control group (IPRP, n = 20). Feasibility and acceptability were evaluated using pre-defined criteria on recruitment- and data collection procedures (e.g., inclusion rates, representativeness, adverse events), physiotherapists’ ratings of trial design and conduct (e.g., acceptability, feasibility), and outcome data characteristics and completeness (e.g., adherence, data accessibility).

Results

Recruitment was largely feasible, though attrition differences and the need for refined eligibility screening were noted. Physiotherapists cited time and implementation challenges. Both groups had satisfactory data completeness, but the control group showed lower adherence to daily reporting in the final third of the study. The intervention group had greater improvements in physical health, with 19.5% more participants achieving the minimum clinically important difference (≥3) on the physical component summary scale (PCS). No adverse events occurred.

Conclusion

With minor adjustments, the R-RCT design is mostly feasible, though some challenges to feasibility were identified and addressed.

Place, publisher, year, edition, pages
Sage Publications, 2024
Keywords
Chronic pain, physical activity, pilot study
National Category
Physiotherapy
Research subject
Health and Welfare, Fysisk aktivitet, rörelsekontroll och muskelaktivitet hos personer med långvarig smärta
Identifiers
urn:nbn:se:du-49732 (URN)10.1177/20552076241299648 (DOI)001363690600001 ()39600393 (PubMedID)
Available from: 2024-11-25 Created: 2024-11-25 Last updated: 2025-02-11Bibliographically approved
Grönkvist, R., Vixner, L., Äng, B. & Grimby-Ekman, A. (2024). Measurement error, minimal detectable change, and minimal clinically important difference of the Short Form-36 Health Survey, Hospital Anxiety and Depression Scale, and Pain Numeric Rating Scale in patients with chronic pain. Journal of Pain, 25(9), Article ID 104559.
Open this publication in new window or tab >>Measurement error, minimal detectable change, and minimal clinically important difference of the Short Form-36 Health Survey, Hospital Anxiety and Depression Scale, and Pain Numeric Rating Scale in patients with chronic pain
2024 (English)In: Journal of Pain, ISSN 1526-5900, E-ISSN 1528-8447, Vol. 25, no 9, article id 104559Article in journal (Refereed) Published
Abstract [en]

In both pain research and clinical practice, patient-reported outcome measures are used to assess dimensions of health. Interpreting these instruments requires understanding their measurement error and what magnitude of change has subjective importance for patients. This study estimated the standard error of measurement (SEM), one-year minimal detectable change, and one-year minimal clinically important difference (MCID) for the Short Form-36 Health Survey physical component summary (SF-36 PCS) and mental (SF36 MCS), the Hospital Anxiety and Depression Scale anxiety symptoms (HADS-A) and depression symptoms (HADS-D) subscales, and the Numeric Rating Scale (NRS) for past-week average pain intensity. MCIDs for these instruments have not previously been estimated in a large sample of chronic pain patients participating in interdisciplinary pain rehabilitation. Data were drawn from the Swedish Quality Registry for Pain Rehabilitation (n=8854 patients). MCID was estimated as average change and change difference, based on three different anchors. MCID estimates were 2.62-4.69 for SF-36 PCS, 4.46-6.79 for SF-36 MCS, 0.895-1.48 for NRS, 1.17-2.13 for HADS-A, and 1.48-2.54 for HADS-D. The common assumption of an identical SEM for pre- and post-treatment measurements was not always applicable. When estimating MCID, researchers should select an estimation method and anchor aligned with the study's context and objectives.

PERSPECTIVE: This article presents estimates of minimal clinically important difference and minimal detectable change for several commonly used patient-reported outcome measures among patients with chronic pain. These estimates can help clinicians and researchers to determine when a measured health improvement is subjectively important to the patient and greater than measurement error.

DATA AVAILABILITY: Data Availability Statement: The data utilized in this study are not available due to ethical considerations and the need for appropriate ethical approval.

Keywords
chronic pain, minimal clinically important difference, minimal detectable change, patient-reported outcome measures
National Category
Clinical Medicine
Identifiers
urn:nbn:se:du-48504 (URN)10.1016/j.jpain.2024.104559 (DOI)001301172800001 ()38734041 (PubMedID)2-s2.0-85194933074 (Scopus ID)
Available from: 2024-05-14 Created: 2024-05-14 Last updated: 2024-09-13Bibliographically approved
Tseli, E., Monnier, A., Lo Martire, R., Vixner, L., Äng, B. & Bohman, T. (2024). Protocol for identifying and characterising critical physical tasks in the military: Development and validation. Work: A journal of Prevention, Assessment and rehabilitation, 77(4), 1261-1272
Open this publication in new window or tab >>Protocol for identifying and characterising critical physical tasks in the military: Development and validation
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2024 (English)In: Work: A journal of Prevention, Assessment and rehabilitation, ISSN 1051-9815, E-ISSN 1875-9270, Vol. 77, no 4, p. 1261-1272Article in journal (Refereed) Published
Abstract [en]

BACKGROUND: When establishing Physical Employment Standards, validity is dependent on the correct identification and characterisation of critical job tasks.

OBJECTIVE: To develop and validate a standardised protocol for the identification, characterisation, and documentation of critical physical job tasks in military occupational specialities in the Swedish Armed Forces (SwAF), and propose a definition of critical physical job tasks for use in the SwAF.

METHODS: A protocol was drafted with three content domains, including a preliminary definition. Protocol content validity was iteratively assessed in two consecutive stages where ten subject experts rated relevance and simplicity. A consensus panel revised the protocol after each stage. Content validity index (CVI) was calculated as item-CVI (I-CVI) per each feature and as scale average (S-CVI/Ave) per content domain. Acceptable content validity thresholds were 0.78 and 0.90, respectively.

RESULTS: The validated protocol consisted of 35 items with an I-CVI≥0.90 and≥0.80 for relevance and simplicity, respectively. The S-CVI/Ave was 0.97 for relevance and 0.98 for simplicity. The protocol was language reviewed, reorganised for easy use, and approved by the consensus panel. The final protocol includes: background and aim of the protocol, the accepted generic and critical physical job task definitions, protocol instructions, subject expert-qualifications, job task source and characteristics.

CONCLUSION: A standardised protocol for identification and characterisation of critical job tasks in SwAF military occupational specialties was developed. The protocol content was rated relevant and simple by experts and will be of importance in future work establishing physical requirements in the SwAF.

Keywords
Evaluation study, military personnel, physical employment standards, questionnaire, work performance
National Category
Occupational Health and Environmental Health
Identifiers
urn:nbn:se:du-48149 (URN)10.3233/WOR-230263 (DOI)001208806800021 ()38393871 (PubMedID)2-s2.0-85190562496 (Scopus ID)
Available from: 2024-02-28 Created: 2024-02-28 Last updated: 2024-06-07Bibliographically approved
Westergren, J., Sjöberg, V., Vixner, L., Nyberg, R. G., Moulaee Conradsson, D., Monnier, A., . . . Äng, B. (2023). Acute exercise as active inference in chronic musculoskeletal pain, effects on gait kinematics and muscular activity in patients and healthy participants: a study protocol for a randomised controlled laboratory trial. BMJ Open, 13(5), Article ID e069747.
Open this publication in new window or tab >>Acute exercise as active inference in chronic musculoskeletal pain, effects on gait kinematics and muscular activity in patients and healthy participants: a study protocol for a randomised controlled laboratory trial
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2023 (English)In: BMJ Open, E-ISSN 2044-6055, Vol. 13, no 5, article id e069747Article in journal (Refereed) Published
Abstract [en]

Introduction

Chronic musculoskeletal pain is a highly prevalent, complex and distressing condition that may negatively affect all domains of life. In view of an active inference framework, and resting on the concept of allostasis, human movement per se becomes a prerequisite for health and well-being while chronic pain becomes a sign of a system unable to attenuate an allostatic load. Previous studies on different subgroups of chronic pain conditions have demonstrated alterations in gait kinematics and muscle activity, indicating shared disturbances in the motor system from long-term allostatic load. We hypothesise that such alterations exist in heterogenous populations with chronic musculoskeletal pain, and that exposure to acute and controlled exercise may attenuate these alterations. Therefore, the main aim of this study is to investigate the acute effects of exercise on gait kinematics and activity of the back and neck muscles during diverse walking conditions in patients with chronic musculoskeletal pain compared with a reference sample consisting of healthy participants.

Methods and analysis

This two-sample two-armed parallel randomised controlled laboratory trial will include 40 participants with chronic musculoskeletal pain (>3 months) and 40 healthy participants. Participants will be randomly allocated to either 30 min of aerobic exercise or rest. Primary outcomes are gait kinematics (walking speed, step frequency, stride length, lumbar rotation, gait stability) and muscular activity (spatial and temporal) of the back and neck during diverse walking conditions. Secondary outcomes are variability of gait kinematics and muscle activity and subjective pain ratings assessed regularly during the trial.

Ethics and dissemination

The study has been approved by the Regional Ethics Review Board in Uppsala, Sweden (#2018/307). Findings will be disseminated via conference presentations, publications in peer-reviewed journals and engagement with patient support groups and clinicians.

Trial registration number

NCT03882333.

National Category
Clinical Medicine
Research subject
Health and Welfare, Fysisk aktivitet, rörelsekontroll och muskelaktivitet hos personer med långvarig smärta
Identifiers
urn:nbn:se:du-46116 (URN)10.1136/bmjopen-2022-069747 (DOI)001007725500001 ()37258077 (PubMedID)2-s2.0-85160705639 (Scopus ID)
Funder
Dalarna University, No grant numberSwedish Research Council, 2015-02512Forte, Swedish Research Council for Health, Working Life and Welfare, 2017-00177Dalarna University, No grant numberSwedish Research Council, 2015-02512Forte, Swedish Research Council for Health, Working Life and Welfare, 2017-00177
Available from: 2023-06-02 Created: 2023-06-02 Last updated: 2023-08-28Bibliographically approved
Tseli, E., Sjöberg, V., Björk, M., Äng, B. & Vixner, L. (2023). Evaluation of content validity and feasibility of the eVISualisation of physical activity and pain (eVIS) intervention for patients with chronic pain participating in interdisciplinary pain rehabilitation programs. PLOS ONE, 18(3), e0282780-e0282780
Open this publication in new window or tab >>Evaluation of content validity and feasibility of the eVISualisation of physical activity and pain (eVIS) intervention for patients with chronic pain participating in interdisciplinary pain rehabilitation programs
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2023 (English)In: PLOS ONE, E-ISSN 1932-6203, Vol. 18, no 3, p. e0282780-e0282780Article in journal (Refereed) Published
National Category
Physiotherapy
Identifiers
urn:nbn:se:du-45742 (URN)10.1371/journal.pone.0282780 (DOI)000988327200001 ()36897847 (PubMedID)2-s2.0-85149784706 (Scopus ID)
Funder
Forte, Swedish Research Council for Health, Working Life and Welfare, 2017-00491Swedish Research Council, 2018-02455Dalarna University
Available from: 2023-04-03 Created: 2023-04-03 Last updated: 2025-02-11Bibliographically approved
Flink, I. K., Engström, J., Vastamäki, S., Vixner, L. & Engman, L. (2023). Expecting the uncertain: The applicability of the intolerance of uncertainty model on fear of childbirth. Journal of Psychosomatic Obstetrics and Gynaecology, 44(1), Article ID 2243648.
Open this publication in new window or tab >>Expecting the uncertain: The applicability of the intolerance of uncertainty model on fear of childbirth
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2023 (English)In: Journal of Psychosomatic Obstetrics and Gynaecology, ISSN 0167-482X, E-ISSN 1743-8942, Vol. 44, no 1, article id 2243648Article in journal (Refereed) Published
Abstract [en]

A considerable number of pregnant women experience fear of childbirth (FOC), characterized by worries and fear of the unpredictable. Despite this, the psychological processes in FOC have received notably little attention. The aim of this study was to advance the understanding by exploring the applicability of the Intolerance of Uncertainty (IU) model on FOC. Anonymous data was collected in a sample of pregnant women (N = 357) with varying levels of FOC. Analyses supported the associations between FOC and all proposed psychological processes: IU, negative problem orientation, positive beliefs about worry and avoidance of inner experiences. The exploration of potential mediators of the relation between IU and FOC revealed that, of the three processes from the model, only positive beliefs about worry were a mediator, and more specifically, a partial mediator between IU and FOC. These findings add to the theoretical understanding of FOC, by indicating that the role of IU may be similar to other conditions inflicted by worry and anxiety, which may inform treatment development. © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

Keywords
childbirth, fear, Fear of childbirth, intolerance of uncertainty, pregnancy, Anxiety, Anxiety Disorders, Female, Humans, Phobic Disorders, Uncertainty, adult, anonymised data, article, avoidance behavior, controlled study, human, human tissue, major clinical study, pregnant woman, theoretical study, anxiety disorder, phobia
National Category
Gynaecology, Obstetrics and Reproductive Medicine Public Health, Global Health, Social Medicine and Epidemiology
Identifiers
urn:nbn:se:du-46832 (URN)10.1080/0167482X.2023.2243648 (DOI)001049679100001 ()37593941 (PubMedID)2-s2.0-85168266757 (Scopus ID)
Available from: 2023-08-28 Created: 2023-08-28 Last updated: 2025-02-11Bibliographically approved
Åhlfeldt, D. A., Vixner, L., Stålnacke, B.-M., Boersma, K., Löfgren, M., Fischer, M. R. & Enthoven, P. (2023). Healthcare Professionals’ Perceptions of and Attitudes towards a Standardized Content Description of Interdisciplinary Rehabilitation Programs for Patients with Chronic Pain: A Qualitative Study. International Journal of Environmental Research and Public Health, 20(9), Article ID 5661.
Open this publication in new window or tab >>Healthcare Professionals’ Perceptions of and Attitudes towards a Standardized Content Description of Interdisciplinary Rehabilitation Programs for Patients with Chronic Pain: A Qualitative Study
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2023 (English)In: International Journal of Environmental Research and Public Health, ISSN 1661-7827, E-ISSN 1660-4601, Vol. 20, no 9, article id 5661Article in journal (Refereed) Published
Abstract [en]

Interdisciplinary pain rehabilitation (IPR) is a recommended treatment for people with chronic pain. An inadequate description of the content of IPR programs makes it difficult to draw conclusions regarding their effects. The purpose of this study was to describe the perceptions and attitudes of healthcare professionals toward a content description of IPR programs for patients with chronic pain. Individual interviews with healthcare professionals (n = 11) working in IPR teams in Sweden were conducted between February and May 2019. Analysis of the interviews resulted in a theme: interdisciplinary pain rehabilitation is a complex intervention, with three categories: limitations in the description of IPR programs; lack of knowledge about IPR and chronic pain; and facilitating and hindering factors for using the content description of IPR programs. Conclusion: Healthcare professionals perceived that IPR programs could be described through a general content description. A general content description could enhance the quality of IPR programs through a better understanding of their content and a comparison of different IPR programs. Healthcare professionals also expressed the importance of a content description being a guide rather than a steering document.

Keywords
interdisciplinary pain rehabilitation; content description; TIDieR checklist; healthcare professionals; complex interventions; individual interviews
National Category
Nursing
Identifiers
urn:nbn:se:du-45940 (URN)10.3390/ijerph20095661 (DOI)37174179 (PubMedID)2-s2.0-85159055565 (Scopus ID)
Available from: 2023-05-02 Created: 2023-05-02 Last updated: 2023-06-02Bibliographically approved
Vixner, L., Hambraeus, K., Äng, B. & Berglund, L. (2023). High Self-Reported Levels of Pain 1 Year After a Myocardial Infarction Are Related to Long-Term All-Cause Mortality: A SWEDEHEART Study Including 18 376 Patients.. Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 12(17), Article ID e029648.
Open this publication in new window or tab >>High Self-Reported Levels of Pain 1 Year After a Myocardial Infarction Are Related to Long-Term All-Cause Mortality: A SWEDEHEART Study Including 18 376 Patients.
2023 (English)In: Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, E-ISSN 2047-9980, Vol. 12, no 17, article id e029648Article in journal (Refereed) Published
Abstract [en]

Background Pain increases the risk for cardiovascular diseases, including myocardial infarction (MI). However, the impact of pain on mortality after MI has not yet been investigated in large studies with long-term follow-up periods. Thus, we aimed to examine various levels of pain severity 1 year after an MI as a potential risk for all-cause mortality. Methods and Results We collected data from 18 376 patients, aged <75 years, who had a registered MI event during the period from 2004 to 2013 and with measurements of potential cardiovascular risk indicators at hospital discharge from the Swedish quality register SWEDEHEART (Swedish Web System for Enhancement and Development of Evidence-Based Care in Heart Disease Evaluated According to Recommended Therapies). Self-reported levels of experienced pain according to EuroQol-5 dimension instrument were recorded in secondary prevention clinics 1 year after hospital discharge. We collected all-cause mortality data up to 8.5 years (median, 3.4 years) after the 1-year visit. The Cox proportional hazard regression was used to estimate hazard ratio (HR) and 95% CI. Moderate pain and extreme pain were reported by 38.2% and 4.5%, respectively, of included patients. There were 1067 deaths. Adjusted HR was 1.35 (95% CI, 1.18-1.55) and 2.06 (95% CI, 1.63-2.60) for moderate and extreme pain, respectively. Pain was a stronger mortality predictor than smoking. Conclusions Pain 1 year after MI is highly prevalent, and its effect on mortality 1 year after MI was found to be more pronounced than smoking. Clinicians managing patients after MI should recognize the need to consider experienced pain when making prognosis or treatment decisions.

Keywords
mortality, myocardial infarction, pain, smoking
National Category
Cardiology and Cardiovascular Disease
Identifiers
urn:nbn:se:du-46837 (URN)10.1161/JAHA.123.029648 (DOI)001062730000044 ()37584219 (PubMedID)2-s2.0-85169847252 (Scopus ID)
Available from: 2023-08-29 Created: 2023-08-29 Last updated: 2025-02-10Bibliographically approved
Sjöberg, V., Tseli, E., Björk, M., Äng, B. & Vixner, L. (2022). 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. In: : . Paper presented at 12th Congress of the European Pain Federation EFIC, Dublin, Ireland, 27-30 April 2022.
Open this publication in new window or tab >>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
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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.

National Category
Physiotherapy
Identifiers
urn:nbn:se:du-41424 (URN)
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: 2025-02-11Bibliographically approved
Projects
Fysisk aktivitet och rörelse hos personer med långvarig smärta. En validerings- och genomförbarhetsstudie, eVIS; Publications
Tseli, E., Sjöberg, V., Björk, M., Äng, B. & Vixner, L. (2023). Evaluation of content validity and feasibility of the eVISualisation of physical activity and pain (eVIS) intervention for patients with chronic pain participating in interdisciplinary pain rehabilitation programs. PLOS ONE, 18(3), e0282780-e0282780Sjöberg, V., Tseli, E., Björk, M., Äng, B. & Vixner, L. (2022). 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. In: : . Paper presented at 12th Congress of the European Pain Federation EFIC, Dublin, Ireland, 27-30 April 2022.
Utvärdering av eVISualisering av fysisk aktivitet och smärta (eVIS) som tillägg till multimodal smärtrehabilitering; Publications
Tseli, E., Sjöberg, V., Björk, M., Äng, B. & Vixner, L. (2023). Evaluation of content validity and feasibility of the eVISualisation of physical activity and pain (eVIS) intervention for patients with chronic pain participating in interdisciplinary pain rehabilitation programs. PLOS ONE, 18(3), e0282780-e0282780Sjöberg, V., Tseli, E., Monnier, A., Westergren, J., LoMartire, R., Äng, B., . . . Vixner, L. (2022). Effectiveness of the eVISualisation of physical activity and pain (eVIS) intervention in Interdisciplinary Pain Rehabilitation Programs: Study Protocol for a Registry-based Randomised Controlled Clinical Trial. In: : . Paper presented at 12th Congress of the European Pain Federation EFIC, Dublin, Ireland, 27-30 April 2022. Sjöberg, V., Tseli, E., Monnier, A., Westergren, J., LoMartire, R., Äng, B., . . . Vixner, L. (2022). Effectiveness of the eVISualisation of physical activity and pain intervention (eVIS) in Swedish Interdisciplinary Pain Rehabilitation Programmes: study protocol for a registry-based randomised controlled clinical trial. BMJ Open, 12(4), Article ID e055071.
Smärta efter hjärtinfarkt - en ökad risk för död?; Publications
Vixner, L., Hambraeus, K., Äng, B. & Berglund, L. (2023). High Self-Reported Levels of Pain 1 Year After a Myocardial Infarction Are Related to Long-Term All-Cause Mortality: A SWEDEHEART Study Including 18 376 Patients.. Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 12(17), Article ID e029648.
Fysisk kravprofil för krigsbefattningar inom Försvarsmakten – utveckling och valideringEtt intelligent och patient-specifikt kliniskt beslutsstödsystem med syfte att effektivisera multimodal specialistvård för patienter med långvarig smärta
Organisations
Identifiers
ORCID iD: ORCID iD iconorcid.org/0000-0002-6923-7140

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