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Systematic Work Environment Model Incorporating Web-based Neck-specific Exercise for Dental Staff With Neck Pain (WorkCIT)

Primary Purpose

Workplace, Neck Pain, Exercise

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
SWEA
Neck-specific exercise
Sponsored by
Linkoeping University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Workplace focused on measuring Neck pain, Workplace, Counseling, Exercise, Internet, Cervical spine

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

For employees:

  • Self-reported WRNP lasting at least 4 weeks
  • Current neck pain ≥ 3 on the numeric rating scale (Numeric Rating Scale (NRS), 0-10)
  • Working age, 18-65 y
  • Neck problems clinically verified by clinical examination to ensure study criteria are met
  • Answered the baseline questionnaire and attended the first intervention visit
  • Completed and signed informed consent, including approval, to contact their immediate supervisor regarding work adaptations.

For managers:

• Being a head/ manager of a dental clinic.

Exclusion Criteria:

Red flags and illness/injury that are contraindicated for or hinder exercise or may be confounding factors for the results including:

  • Known pregnancy
  • Cannot understand/communicate in Swedish and would be unable to understand information about the study or answer questionnaires.

For blood samples (not wanting to participate does not constitute exclusion from the RCT), the following exclusion criteria are added:

• Increased tendency to bleed and use of blood thinners.

For the microdialysis subgroup (n=30), consecutively asked, 15 persons/group; not wanting to participate does not constitute exclusion from the RCT), the following exclusion criteria are added:

  • Cannot imagine refraining from anti-inflammatory drugs (NSAIDs) during the 2 days prior to microdialysis
  • Hypersensitivity

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Experimental

    Arm Label

    Managerial support in using systematic work environment evaluation and adjustment (SWEA)

    Neck-specific exercise in addition to SWEA

    Arm Description

    Managerial support in using SWEA and the Prehab guide to enhance employees' work situation. Individual work adaptations are adaptations to everyone´s ability in the physical, organisational, and social work environment that aim to enable an employee with reduced ability to perform the normal work, continue working, or plan for a sustainable return to work. The Prehab guide contains a self-assessment test for the employee based on the requirements of the work and one's own ability that can be used in the dialogue with the manager. It also contains suggestions for activities to create a healthier workplace, such as discovering early signals of stress or pain, creating a caring workplace culture and boundaries, regular contact with an employee that is on sick-leave, clear and established safety procedures and routines for the work environmental work, routines for cooperation with other parties, and to learn from one's own and colleague's experiences in an open, permissive climate.

    NSEs will be performed based on a well-structured framework of evidence-based exercises for facilitation of deep neck muscles, improved interaction between the different muscle layers of the neck, increased neck muscle endurance, and improved postural control [15, 30]. To ensure that the exercises are learned and performed correctly, the participant will meet with a physiotherapist a total of four times, once during weeks 2, 3, 4, and 7 (week 1=first visit for a clinical examination due to law) for instruction, guidance, and support. In addition to photos, videos, and text regarding the exercises, the digital support (web-based program at the support and treatment platform Inera via 1177 managed by the County Councils) also contains information about why it is important to exercise the neck muscles, factors that may cause neck pain, how relapses can be handled, ergonomic advice related to the neck, and an exercise diary.

    Outcomes

    Primary Outcome Measures

    Current neck pain intensity
    Current neck pain intensity at 15 months follow-up measured on the numeric rating scale (NRS) (0=no pain and 10=worst imaginable pain)

    Secondary Outcome Measures

    Work Ability Index (WAI) including Work Ability Scale (question no 1 in WAI)
    Current work ability compared to when it was at its best, total score, between 7 and 49, poor (7-27), moderate (28-36), good (37-43) and excellent (44-49) work ability
    Intensity of pain and bothersomeness
    neck pain bothersomeness, headache intensity on NRS
    Frequency of pain, symptoms and medications
    Frequency of pain, pain medication, neck stiffness, numbness/tingling into the arms, having problems lifting the arms, dizziness, sleep, concentration.
    Neck specific function
    Neck Disability Index, 0 to 50 points or 0 to 100%; 0= no disability
    Symptom satisfaction
    Symptom satisfaction; how patients would feel about having their current (the last 24-hours) neck symptoms for the rest of thir lives, 1=delighted, 7=terrible (according to Cherkin and Deyo)
    Exercise/ Physical activity level
    Exercise/ physical activity level, how much time do you spend a regular week doing physical exercise and regular physical exercise, respectively, in median minutes, more minutes= better
    Health related quality of life, EQ-5D-5L
    Euroqol 5 dimension; EQ-5D-5L, The descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems, a summed score of all 5 questions will be used where 1=perfect health.
    Perceived exertion at work
    Borg scale of exertion, ratings of perceived exertion at work measured with the Borg scale; 0=no exertion, 10=major exertion
    Sick-leave
    sick leave numbers of days/month
    Effort-Reward Imbalance
    Effort-Reward Imbalance questionnaire, less than 1 is indicating a favour of rewards, more than 1 indicating a favour of effort
    Risk identification at work
    Structured multidisciplinary work evaluation tool, (SMET) will be used. The questionnaire asks about physically, environmentally and psychosocially demanding work items (30 items). A scale of 1-10 is used in the questionnaire, 1 is labeled "Not at all" and 10 is labeled "Highly".
    Work adaptation
    Open questions about work adaptation, such as self strategies to be able to work
    Time sitting
    Time sitting at work and during leisure time
    Anxiety and depression
    Hospital Anxiety and Depression Scale, 0-6= healthy, 7-10= mild to moderate, >10= (risk for/ indication of- a diagnos needs a clinical examination) anxiety or depression
    Fullfilment of treatment expectation
    Fullfilment of treatment expectation, have your expectations been fullfilled, yes, yes partly, no
    Overall outcome
    Global rating of change scale, -5= much worse, 0= unchanged, 5=much better/restored
    Satisfaction with the caregiver visits in the study
    Patient enablement questionnaire, The PEI is a 6-item scale that has been used in general prac-tice to evaluate quality of care. The highest possible score is 12, with higher scores indicating greater enablement.
    Cost-effectiveness. (Will be analysed in a later stage if differences appear between groups)
    Through calculation of direct costs; quantity and type of care (inside and outside the study also including drugs related to pain) from registers and from questionnaires, indirect costs; mainly production loss from registers and from questionnaire. Will be calculated if there is a difference between randomisation groups and will in that case be presented in a paper of its own.
    Saliva samples and blood samples (Sub-group, not in the RCT)
    Experimental sub-group study. Protein analysis to investigate differences between patients and healthy controls, biomarkers of inflammation and stress. Will be performed in a sub-group. Saliva will be collected with Salivette. Venous blood samples (10-20 ml) from the elbow fold will be collected in EDTA tubes. Identification and quantification of proteins. In a subgroup of the RCT population. Comparisons will be made with healthy controls. Permits for biobank is available.
    Microdialysis, tissue changes in the middle of Trapezius (Subgroup study, not in the RCT)
    Biomechanical changes interstitialli in M. Trapezius. Through microdialysis technology, it is possible to monitor biochemical changes interstitially in the tissue. The technique involves the exchange of substances via diffusion between the tissue and a diaphragmatic cateter inserted into the tissue and flushed by a fluid (perfusate) that is similar in chemical composition to the fluid in the muscle interstitium. Comparisons will be made with healthy controls.
    Interview study of employees (Sub-group study, not in the RCT)
    Employees experience with interventions and their impact on work ability, health and work situation. Sub-group of the RCT population.
    Interview with managers (Subgroup study)
    Interview with managers regarding the experience of using SWEA and the Prehabguide. A subgroup will be interviewd, Approximately n=approximately 15.
    Perceived work environment problems
    During the past 7 days, how much did your work environment-related problemsaffect your performance at work? A scale 0 - 10 is used, 0 is labeled " Workenvironment problems have not affected my work performance" and 10 is labeled"Work environment problems completely prevented me from working". A higher score indicates a worse outcome.
    Work environment related production loss
    During the past 7 days, how much did your work environment-related problemsaffect your performance at work? A scale 0 - 10 is used, 0 is labeled " Workenvironment problems have not affected my work performance" and 10 is labeled"Work environment problems completely prevented me from working". A higherscore indicates a worse outcome.
    Self-rated work situation regarding neck position at work
    Numeric rating scale 0-10, 10= very satisfied
    Health related quality of life, EQ thermometer
    Euroqol vertical visual analogue scale, 0-100, 100=perfect health

    Full Information

    First Posted
    June 28, 2022
    Last Updated
    July 7, 2022
    Sponsor
    Linkoeping University
    Collaborators
    Ostergotland County Council, Sweden, Lund University, Karlstad University, The University of Queensland, Sormland County Council, Sweden
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05447858
    Brief Title
    Systematic Work Environment Model Incorporating Web-based Neck-specific Exercise for Dental Staff With Neck Pain
    Acronym
    WorkCIT
    Official Title
    Systematic Work Environment Model Incorporating Web-based Neck-specific Exercise for Dental Staff With Neck Pain: A Prospective Randomized Controlled Study (WorkCIT)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    January 9, 2023 (Anticipated)
    Primary Completion Date
    December 31, 2025 (Anticipated)
    Study Completion Date
    December 31, 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Linkoeping University
    Collaborators
    Ostergotland County Council, Sweden, Lund University, Karlstad University, The University of Queensland, Sormland County Council, Sweden

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The aim of study; WorkCIT is to investigate whether managerial support in using systematic work environment evaluation and adjustment (SWEA) with/without additional 3 month web-based NSEs with four visits to a physiotherapist is effective in promoting reduced neck pain and disability among dental health care professionals (DHCP) with work-related neck pain (WRNP). The aim of the subgroup studies is to investigate biomarkers and tissue changes and the association with pain, work ability, and other outcomes before and after SWEA with or without NSEs. Furthermore, to investigate dental staff experiences with the interventions and their impact on work ability, health and their work situation, and investigate managers experience of SWEA with support from the Prehab guide and workshops. The hypothesis is that a combined effort with SWEA to promote the work situation together with NSEs will reduce neck pain intensity and improve work ability to a greater extent than the SWEA only. Methods and analysis: This is a prospective, longitudinal, randomised, controlled multi-centre trial with two parallel treatment arms and blinded investigators conducted according to a detailed protocol following the guidelines in the CONSORT checklist. A total of 240 DHCP with WRNP will be recruited. The main outcome is neck pain intensity. Secondary outcomes are work ability, function, health-related quality of life, work absenteeism, work-related factors, and work adjustments made. Cost-effectiveness will be studied from a societal perspective if significant differences appear between randomization groups regarding health-related quality of life and will in that case be reported in a separate paper. To improve diagnostics and help assess the effectiveness of intervention biochemical sub-group studies will be performed before and after intervention to investigate pain related biomarkers. Interviews with a sub-group of participants and managers will be performed regarding work-ability, work adjustments and experiences of interventions.
    Detailed Description
    Introduction: Neck pain among dental health care professionals (DHCP) is a growing societal problem. It is compulsory by law, for managers to work with systematic work environment evaluation and adjustment (SWEA), though managers knowledge of this approach is often deficient. Managerial support in using SWEA to enhance employees' work situation has not been investigated in regards to work-related neck pain (WRNP). Clear guidelines on interventions for WRNP are lacking. Neck-specific exercise (NSE) is the method with the most evidence regarding treatment for neck problems in general but has not been investigated for WRNP. The aim of study; WORKCIT is to investigate whether managerial support in using SWEA with/without additional 3 month web-based NSEs with four visits to a physiotherapist is effective in promoting reduced neck pain and disability among DHCP with WRNP. More specifically, the main project aims to: Compare the effects of SWEA with a focus on adjustments at work and support for DHCP (aimed for all staff) by their manager with the addition (half of the staff) of an E-health solution of NSEs in combination with four visits to a physiotherapist with regards to neck pain intensity, disability, work ability, health, and cost-effectiveness; Investigate whether a participatory approach of workshops and digital education for managers in SWEA/ Prehabguiden Suntarbetsliv (Prehab guide) enhance the work environment (organisational, social, and physical), including individual support and adjustment of the work situation, reducing their neck pain intensity; Investigate if NSE reduces WRNP in addition to SWEA; Identify underlying factors associated with the outcome following work interventions with or without exercise regarding pain, work ability, and health. The aim of the subgroup studies is to investigate biomarkers and tissue changes and the association with pain, work ability, and other outcomes before and after SWEA with or without NSEs. Furthermore, to investigate dental staff experiences with the interventions and their impact on work ability, health and their work situation, and investigate managers experience of SWEA with support from the Prehab guide and workshops. The hypothesis is that a combined effort with SWEA to promote the work situation together with NSEs will reduce neck pain intensity and improve work ability to a greater extent than the SWEA only. Methods and analysis: This is a prospective, longitudinal, randomised, controlled multi-centre trial with two parallel treatment arms and blinded investigators conducted according to a detailed protocol following the guidelines in the CONSORT checklist. A total of 240 DHCP with WRNP will be recruited. The main outcome is neck pain intensity. Secondary outcomes are work ability, function, health-related quality of life, work absenteeism, work-related factors, and work adjustments made. Cost-effectiveness will be studied from a societal perspective if significant differences appear between randomization groups regarding health-related quality of life and will in that case be reported in a separate paper. To improve diagnostics and help assess the effectiveness of intervention biochemical sub-group studies will be performed before and after intervention to investigate pain related biomarkers. Interviews with a sub-group of participants and managers will be performed regarding work-ability, work adjustments and experiences of interventions. Ethics and dissemination: The study is approved by the Swedish Ethical Review Authority. The processing of personal data according to the General Data Protection Regulation will be registered at Linköping University before the start of the study. The results will be published in scientific journals, presented at scientific conferences and in meetings with caregivers, disseminated in lectures to the medical faculty and patient associations, and communicated in the media.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Workplace, Neck Pain, Exercise
    Keywords
    Neck pain, Workplace, Counseling, Exercise, Internet, Cervical spine

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Randomization will be handled by a person not involved in intervention or evaluation. Investigators/ assessors will be blinded for randomization. This is a prospective, longitudinal, randomised, controlled multi-centre trial with two parallel treatment arms and blinded investigators conducted according to a detailed protocol. A total of 240 employees with WRNP will be recruited. The main outcome is neck pain intensity. Secondary outcomes are work ability, function, health-related quality of life, work absenteeism, work-related factors, work adjustments made. Cost-effectiveness will be studied if significant differences appear between randomization groups regarding health-related quality of life and will in that case be reported in a separate paper.
    Masking
    InvestigatorOutcomes Assessor
    Masking Description
    Double (Investigator, Outcomes Assessor)
    Allocation
    Randomized
    Enrollment
    240 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Managerial support in using systematic work environment evaluation and adjustment (SWEA)
    Arm Type
    Active Comparator
    Arm Description
    Managerial support in using SWEA and the Prehab guide to enhance employees' work situation. Individual work adaptations are adaptations to everyone´s ability in the physical, organisational, and social work environment that aim to enable an employee with reduced ability to perform the normal work, continue working, or plan for a sustainable return to work. The Prehab guide contains a self-assessment test for the employee based on the requirements of the work and one's own ability that can be used in the dialogue with the manager. It also contains suggestions for activities to create a healthier workplace, such as discovering early signals of stress or pain, creating a caring workplace culture and boundaries, regular contact with an employee that is on sick-leave, clear and established safety procedures and routines for the work environmental work, routines for cooperation with other parties, and to learn from one's own and colleague's experiences in an open, permissive climate.
    Arm Title
    Neck-specific exercise in addition to SWEA
    Arm Type
    Experimental
    Arm Description
    NSEs will be performed based on a well-structured framework of evidence-based exercises for facilitation of deep neck muscles, improved interaction between the different muscle layers of the neck, increased neck muscle endurance, and improved postural control [15, 30]. To ensure that the exercises are learned and performed correctly, the participant will meet with a physiotherapist a total of four times, once during weeks 2, 3, 4, and 7 (week 1=first visit for a clinical examination due to law) for instruction, guidance, and support. In addition to photos, videos, and text regarding the exercises, the digital support (web-based program at the support and treatment platform Inera via 1177 managed by the County Councils) also contains information about why it is important to exercise the neck muscles, factors that may cause neck pain, how relapses can be handled, ergonomic advice related to the neck, and an exercise diary.
    Intervention Type
    Other
    Intervention Name(s)
    SWEA
    Intervention Description
    Managers with one or several l staff experiencing WRNP will be educated in the Prehab guide. The manager should read and listen to all modules and a 1-h lecture recorded by the research team before participating in two workshops (4 h each), together with other managers and an experienced expert in work environmental health and rehabilitation. In the workshops, different themes will be discussed, such as physical, psychological, and organisational work-related health, prevention, and rehabilitation, how to lead problem-solving dialogue, how work-related adaptations can be performed related to WRNP, and questions about the Prehab guide. The Prehab guide will be used to deliver managerial support in the work with the Swedish Work Environment Authority's regulations regarding SWEA and the prevention of ill health, sick leave, and accidents, work adaptations, and workplace-oriented rehabilitation.
    Intervention Type
    Other
    Intervention Name(s)
    Neck-specific exercise
    Intervention Description
    NSEs will be performed based on a well-structured framework of evidence-based exercises for facilitation of deep neck muscles, improved interaction between the different muscle layers of the neck, increased neck muscle endurance, and improved postural control .
    Primary Outcome Measure Information:
    Title
    Current neck pain intensity
    Description
    Current neck pain intensity at 15 months follow-up measured on the numeric rating scale (NRS) (0=no pain and 10=worst imaginable pain)
    Time Frame
    Change in current neck pain intensity from baseline, to 3 month (after intervention) and until the 15 month follow-up (1 year after intervention ended).
    Secondary Outcome Measure Information:
    Title
    Work Ability Index (WAI) including Work Ability Scale (question no 1 in WAI)
    Description
    Current work ability compared to when it was at its best, total score, between 7 and 49, poor (7-27), moderate (28-36), good (37-43) and excellent (44-49) work ability
    Time Frame
    Change in work ability from baseline to 3 month and 15 month follow-up
    Title
    Intensity of pain and bothersomeness
    Description
    neck pain bothersomeness, headache intensity on NRS
    Time Frame
    Change from baseline to 3 month and 15 month follow-up
    Title
    Frequency of pain, symptoms and medications
    Description
    Frequency of pain, pain medication, neck stiffness, numbness/tingling into the arms, having problems lifting the arms, dizziness, sleep, concentration.
    Time Frame
    Change from baseline to 3 month and 15 month follow-up
    Title
    Neck specific function
    Description
    Neck Disability Index, 0 to 50 points or 0 to 100%; 0= no disability
    Time Frame
    Change from baseline to 3 month and 15 month follow-up
    Title
    Symptom satisfaction
    Description
    Symptom satisfaction; how patients would feel about having their current (the last 24-hours) neck symptoms for the rest of thir lives, 1=delighted, 7=terrible (according to Cherkin and Deyo)
    Time Frame
    Change from baseline to 3 month and 15 month follow-up
    Title
    Exercise/ Physical activity level
    Description
    Exercise/ physical activity level, how much time do you spend a regular week doing physical exercise and regular physical exercise, respectively, in median minutes, more minutes= better
    Time Frame
    Change from baseline to 3 month and 15 month follow-up
    Title
    Health related quality of life, EQ-5D-5L
    Description
    Euroqol 5 dimension; EQ-5D-5L, The descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems, a summed score of all 5 questions will be used where 1=perfect health.
    Time Frame
    Change from baseline to 3 month and 15 month follow-up
    Title
    Perceived exertion at work
    Description
    Borg scale of exertion, ratings of perceived exertion at work measured with the Borg scale; 0=no exertion, 10=major exertion
    Time Frame
    Change from baseline to 3 month and 15 month follow-up
    Title
    Sick-leave
    Description
    sick leave numbers of days/month
    Time Frame
    Change from baseline to 3 month and 15 month follow-up
    Title
    Effort-Reward Imbalance
    Description
    Effort-Reward Imbalance questionnaire, less than 1 is indicating a favour of rewards, more than 1 indicating a favour of effort
    Time Frame
    Change from baseline to 3 month and 15 month follow-up
    Title
    Risk identification at work
    Description
    Structured multidisciplinary work evaluation tool, (SMET) will be used. The questionnaire asks about physically, environmentally and psychosocially demanding work items (30 items). A scale of 1-10 is used in the questionnaire, 1 is labeled "Not at all" and 10 is labeled "Highly".
    Time Frame
    Change from baseline to 3 month and 15 month follow-up
    Title
    Work adaptation
    Description
    Open questions about work adaptation, such as self strategies to be able to work
    Time Frame
    Change from baseline to 3 month and 15 month follow-up
    Title
    Time sitting
    Description
    Time sitting at work and during leisure time
    Time Frame
    Change from baseline to 3 month and 15 month follow-up
    Title
    Anxiety and depression
    Description
    Hospital Anxiety and Depression Scale, 0-6= healthy, 7-10= mild to moderate, >10= (risk for/ indication of- a diagnos needs a clinical examination) anxiety or depression
    Time Frame
    Change from baseline to 3 month and 15 month follow-up
    Title
    Fullfilment of treatment expectation
    Description
    Fullfilment of treatment expectation, have your expectations been fullfilled, yes, yes partly, no
    Time Frame
    Change from baseline to 3 month and 15 month follow-up
    Title
    Overall outcome
    Description
    Global rating of change scale, -5= much worse, 0= unchanged, 5=much better/restored
    Time Frame
    Cross-sectional 3 month and 15 month follow-up
    Title
    Satisfaction with the caregiver visits in the study
    Description
    Patient enablement questionnaire, The PEI is a 6-item scale that has been used in general prac-tice to evaluate quality of care. The highest possible score is 12, with higher scores indicating greater enablement.
    Time Frame
    Cross-sectional 3 month and 15 month follow-up
    Title
    Cost-effectiveness. (Will be analysed in a later stage if differences appear between groups)
    Description
    Through calculation of direct costs; quantity and type of care (inside and outside the study also including drugs related to pain) from registers and from questionnaires, indirect costs; mainly production loss from registers and from questionnaire. Will be calculated if there is a difference between randomisation groups and will in that case be presented in a paper of its own.
    Time Frame
    From the time period between baseline to 15 month follow-up
    Title
    Saliva samples and blood samples (Sub-group, not in the RCT)
    Description
    Experimental sub-group study. Protein analysis to investigate differences between patients and healthy controls, biomarkers of inflammation and stress. Will be performed in a sub-group. Saliva will be collected with Salivette. Venous blood samples (10-20 ml) from the elbow fold will be collected in EDTA tubes. Identification and quantification of proteins. In a subgroup of the RCT population. Comparisons will be made with healthy controls. Permits for biobank is available.
    Time Frame
    Change from baseline to 3-month follow-up in the subgroup of the RCT population
    Title
    Microdialysis, tissue changes in the middle of Trapezius (Subgroup study, not in the RCT)
    Description
    Biomechanical changes interstitialli in M. Trapezius. Through microdialysis technology, it is possible to monitor biochemical changes interstitially in the tissue. The technique involves the exchange of substances via diffusion between the tissue and a diaphragmatic cateter inserted into the tissue and flushed by a fluid (perfusate) that is similar in chemical composition to the fluid in the muscle interstitium. Comparisons will be made with healthy controls.
    Time Frame
    Change from baseline to 3 month, subgroup of the RCT population
    Title
    Interview study of employees (Sub-group study, not in the RCT)
    Description
    Employees experience with interventions and their impact on work ability, health and work situation. Sub-group of the RCT population.
    Time Frame
    after intervention fulfilled, sub-group of the RCT population, n=approximately 15
    Title
    Interview with managers (Subgroup study)
    Description
    Interview with managers regarding the experience of using SWEA and the Prehabguide. A subgroup will be interviewd, Approximately n=approximately 15.
    Time Frame
    After having at least one employee participating and fulfilled the study.
    Title
    Perceived work environment problems
    Description
    During the past 7 days, how much did your work environment-related problemsaffect your performance at work? A scale 0 - 10 is used, 0 is labeled " Workenvironment problems have not affected my work performance" and 10 is labeled"Work environment problems completely prevented me from working". A higher score indicates a worse outcome.
    Time Frame
    Description and change from baseline to 3 month and 15 month follow-up
    Title
    Work environment related production loss
    Description
    During the past 7 days, how much did your work environment-related problemsaffect your performance at work? A scale 0 - 10 is used, 0 is labeled " Workenvironment problems have not affected my work performance" and 10 is labeled"Work environment problems completely prevented me from working". A higherscore indicates a worse outcome.
    Time Frame
    Description and change from baseline to 3 month and 15 month follow-up
    Title
    Self-rated work situation regarding neck position at work
    Description
    Numeric rating scale 0-10, 10= very satisfied
    Time Frame
    Description and change from baseline to 3 month and 15 month follow-up
    Title
    Health related quality of life, EQ thermometer
    Description
    Euroqol vertical visual analogue scale, 0-100, 100=perfect health
    Time Frame
    Change from baseline to 3 and 15 months
    Other Pre-specified Outcome Measures:
    Title
    Profession
    Description
    Swedish standard for work classification
    Time Frame
    Baseline
    Title
    Background data
    Description
    Age, sex, education, family situation, pain duration, expectations, smoking history
    Time Frame
    Baseline
    Title
    Treatment outside the study
    Description
    A in-house made question about treatment outside the study at different health care professionals, number of visits and if better or unchanged and earlier treatment for neck pain before inclusion into the study
    Time Frame
    Descripton baseline, 3 month, 15 month
    Title
    Profession
    Description
    Open question of profession
    Time Frame
    Description baseline, 3 month and 15 month
    Title
    work situation
    Description
    Description of occupation, work tasks, type of employer, working hours, years in occupation, in-house made questions as basic background information to understand each workers work situation and change in work sitiation
    Time Frame
    Descriptive data at baseline, 3 month and 15 month follow-up

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: For employees: Self-reported WRNP lasting at least 4 weeks Current neck pain ≥ 3 on the numeric rating scale (Numeric Rating Scale (NRS), 0-10) Working age, 18-65 y Neck problems clinically verified by clinical examination to ensure study criteria are met Answered the baseline questionnaire and attended the first intervention visit Completed and signed informed consent, including approval, to contact their immediate supervisor regarding work adaptations. For managers: • Being a head/ manager of a dental clinic. Exclusion Criteria: Red flags and illness/injury that are contraindicated for or hinder exercise or may be confounding factors for the results including: Known pregnancy Cannot understand/communicate in Swedish and would be unable to understand information about the study or answer questionnaires. For blood samples (not wanting to participate does not constitute exclusion from the RCT), the following exclusion criteria are added: • Increased tendency to bleed and use of blood thinners. For the microdialysis subgroup (n=30), consecutively asked, 15 persons/group; not wanting to participate does not constitute exclusion from the RCT), the following exclusion criteria are added: Cannot imagine refraining from anti-inflammatory drugs (NSAIDs) during the 2 days prior to microdialysis Hypersensitivity
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Anneli Peolsson, Prof., PhD
    Phone
    +46-700850599
    Email
    Anneli.Peolsson@liu.se
    First Name & Middle Initial & Last Name or Official Title & Degree
    Charlotte Wåhlin, A. Prof., PhD
    Phone
    +46-101036267
    Email
    Charlotte.Wahlin@regionostergotland.se
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Anneli Peolsson, Prof., PhD
    Organizational Affiliation
    Linkoeping University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    IPD Sharing Plan Description
    The data is protected by the Swedish health secrets act and the European General Data Protection Regulation. Data will be presented on a group level without possibility for individual identification.

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    Systematic Work Environment Model Incorporating Web-based Neck-specific Exercise for Dental Staff With Neck Pain

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