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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
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 1875-9270Article in journal (Refereed) Epub ahead of print
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)38393871 (PubMedID)
Available from: 2024-02-28 Created: 2024-02-28 Last updated: 2024-02-28Bibliographically 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: 2023-10-03Bibliographically 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
Obstetrics, Gynecology 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: 2023-09-04Bibliographically 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, ISSN 2047-9980, 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
Cardiac and Cardiovascular Systems
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: 2023-11-20Bibliographically 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: 2022-05-12Bibliographically approved
Sjöberg, 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.
Open this publication in new window or tab >>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
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2022 (English)Conference paper, Poster (with or without abstract) (Refereed)
Abstract [en]

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.

National Category
Physiotherapy
Identifiers
urn:nbn:se:du-41423 (URN)
Conference
12th Congress of the European Pain Federation EFIC, Dublin, Ireland, 27-30 April 2022
Funder
Forte, Swedish Research Council for Health, Working Life and Welfare, 2017-00491
Available from: 2022-05-11 Created: 2022-05-11 Last updated: 2023-10-03Bibliographically approved
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.
Open this publication in new window or tab >>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
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2022 (English)In: BMJ Open, E-ISSN 2044-6055, Vol. 12, no 4, article id e055071Article in journal (Refereed) Published
Abstract [en]

Introduction Living with chronic pain often involves negative consequences. Interdisciplinary Pain Rehabilitation Programmes (IPRP) is considered superior to single-treatment measures in patients with chronic pain. Despite this, effects emerge suboptimal and more than 20% of patients deteriorate in patientreported physical health outcomes after IPRP. A novel e-Health intervention, eVISualisation (eVIS) of physical activity and pain, was systematically developed to facilitate individualisation of physical activity levels. By adding elements of data collection, visualisation and communication of objectively measured physical activity and patient-reported outcomes (pain intensity, interference of pain, pharmaceutical consumption) to existing treatment modalities in IPRP, the IPRP team acquires prerequisites to adapt advice and physical activity prescriptions and to evaluate set activity goals. The overall aim is two fold. First, the aim is to evaluate the feasibility of the subsequent registry-based randomised controlled clinical trial (R-RCT). Second, the aim is to prospectively evaluate the effectiveness of the eVISintervention as a supplement to IPRP on our defined primary (physical health) and secondary outcomes.

Methods and analysis In the R-RCT, recruitment of 400 patients with chronic pain will be performed at 15 IPRP units. A random allocation to either IPRP + eVIS or to control group that will receive IPRP only will be performed. Data from the initial 30 participants completing the study period (6 months) will be included in a pilot study, where key feasibility outcomes (recruitment, randomisation, implementation, treatment integrity, data collection procedure, preliminary outcome measures) will be evaluated. Outcome variables will be extracted from the web application Pain And TRaining ON-line (PATRON) and from six national registries. Multivariate statistics and repeated measure analyses will be performed. Quality-adjusted life years and incremental cost-effectiveness ratio will be calculated for cost-effectiveness evaluation.

Ethics/dissemination The Swedish Ethics Review Board granted approval (Dnr 2021/02109). Results will be disseminated through peer-reviewed journals.

Trial registration number NCT05009459. Protocol V.1

Keywords
pain management; protocols & guidelines; telemedicine
National Category
Physiotherapy
Identifiers
urn:nbn:se:du-41275 (URN)10.1136/bmjopen-2021-055071 (DOI)000783842400053 ()35428627 (PubMedID)2-s2.0-85128487846 (Scopus ID)
Funder
Forte, Swedish Research Council for Health, Working Life and Welfare, 2017-00491Swedish Research Council
Available from: 2022-04-18 Created: 2022-04-18 Last updated: 2023-08-28Bibliographically approved
Turesson, C., Liedberg, G., Vixner, L., Lofgren, M. & Björk, M. (2022). Evidence-based digital support during 1 year after an Interdisciplinary Pain Rehabilitation Programme for persons with chronic musculoskeletal pain to facilitate a sustainable return to work: a study protocol for a registry-based multicentre randomised controlled trial. BMJ Open, 12(4), Article ID e060452.
Open this publication in new window or tab >>Evidence-based digital support during 1 year after an Interdisciplinary Pain Rehabilitation Programme for persons with chronic musculoskeletal pain to facilitate a sustainable return to work: a study protocol for a registry-based multicentre randomised controlled trial
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2022 (English)In: BMJ Open, E-ISSN 2044-6055, Vol. 12, no 4, article id e060452Article in journal (Refereed) Published
Abstract [en]

INTRODUCTION: Chronic musculoskeletal pain (CMSP) severely affects the individual's quality of life, functioning and ability to work, and comes with significant societal costs for sick leave and productivity loss. After rehabilitation, patients with CMSP often experience lack of support when responsibility for the return-to-work process is taken over by the employer. Therefore, we aim to evaluate the effectiveness of a digital support (Sustainable WorkEr digital support for Persons with chronic Pain and their Employers (SWEPPE)) for promoting a sustainable return-to-work for persons with CMSP and to facilitate the employers' supportive role and responsibilities in the process.

METHODS AND ANALYSIS: In this registry-based multicentre randomised controlled trial, 360 patients with CMSP will be randomised to either receive the smartphone application SWEPPE (n=180) or to a control group (n=180). The intervention group will use SWEPPE for 1 year and the control group will not receive any intervention for return to work (RTW). Participants will be recruited from approximately 10 specialist and primary care level units connected to the Swedish National Quality Registry for Pain Rehabilitation providing Interdisciplinary Pain Rehabilitation Programmes (IPRP) for CMSP. Eligibility criteria are age 18-65 years and a need for support in RTW or continued support at work for creating a sustainable work situation. Baseline data will be collected when the participants have completed the IPRP. Final assessment will be performed after 12 months. The primary outcome will be a number of days with sickness cash benefit. Secondary outcomes and explanatory variables including important domains affected by CMSP such as health-related quality of life, functioning and work ability will be collected.

ETHICS AND DISSEMINATION: The Swedish Ethics Review Board approved the study (Dnr 2020-01593, Dnr 2021-01854). The study findings will be disseminated through publication, national and international conferences, and meetings to be available for patients, healthcare providers or stakeholders.

TRIAL REGISTRATION NUMBER: NCT05058547.

Keywords
Clinical trials, PAIN MANAGEMENT, REHABILITATION MEDICINE
National Category
Clinical Medicine
Identifiers
urn:nbn:se:du-41399 (URN)10.1136/bmjopen-2021-060452 (DOI)000787816100009 ()35470201 (PubMedID)2-s2.0-85128836680 (Scopus ID)
Available from: 2022-05-06 Created: 2022-05-06 Last updated: 2023-08-28Bibliographically 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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