Exercise, Neck Pain, Workplace
Conditions
Keywords
Neck pain, Workplace, Counseling, Exercise, Internet, Cervical spine
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.
Interventions
OTHERSWEA
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.
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 .
Sponsors
Ostergotland County Council, Sweden
Lund University
Karlstad University
The University of Queensland
Sormland County Council, Sweden
Linkoeping University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)
Masking description
Double (Investigator, Outcomes Assessor)
Intervention 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.
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Current neck pain intensity | 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). | 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
| Measure | Time frame | Description |
|---|---|---|
| Work adaptation | Change from baseline to 3 month and 15 month follow-up | Open questions about work adaptation, such as self strategies to be able to work |
| Perceived work environment problems | Description and change from baseline to 3 month and 15 month follow-up | 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 labeledWork environment problems completely prevented me from working. A higher score indicates a worse outcome. |
| Work environment related production loss | Description and change from baseline to 3 month and 15 month follow-up | 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 labeledWork environment problems completely prevented me from working. A higherscore indicates a worse outcome. |
| Self-rated work situation regarding neck position at work | Description and change from baseline to 3 month and 15 month follow-up | Numeric rating scale 0-10, 10= very satisfied |
| Health related quality of life, EQ thermometer | Change from baseline to 3 and 15 months | Euroqol vertical visual analogue scale, 0-100, 100=perfect health |
| Work Ability Index (WAI) including Work Ability Scale (question no 1 in WAI) | Change in work ability from baseline to 3 month and 15 month follow-up | 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 | Change from baseline to 3 month and 15 month follow-up | neck pain bothersomeness, headache intensity on NRS |
| Frequency of pain, symptoms and medications | Change from baseline to 3 month and 15 month follow-up | Frequency of pain, pain medication, neck stiffness, numbness/tingling into the arms, having problems lifting the arms, dizziness, sleep, concentration. |
| Neck specific function | Change from baseline to 3 month and 15 month follow-up | Neck Disability Index, 0 to 50 points or 0 to 100%; 0= no disability |
| Symptom satisfaction | Change from baseline to 3 month and 15 month follow-up | 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 | Change from baseline to 3 month and 15 month follow-up | 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 | Change from baseline to 3 month and 15 month follow-up | 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 | Change from baseline to 3 month and 15 month follow-up | Borg scale of exertion, ratings of perceived exertion at work measured with the Borg scale; 0=no exertion, 10=major exertion |
| Sick-leave | Change from baseline to 3 month and 15 month follow-up | sick leave numbers of days/month |
| Effort-Reward Imbalance | Change from baseline to 3 month and 15 month follow-up | 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 | Change from baseline to 3 month and 15 month follow-up | 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 sitting | Change from baseline to 3 month and 15 month follow-up | Time sitting at work and during leisure time |
| Anxiety and depression | Change from baseline to 3 month and 15 month follow-up | 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 | Change from baseline to 3 month and 15 month follow-up | Fullfilment of treatment expectation, have your expectations been fullfilled, yes, yes partly, no |
| Overall outcome | Cross-sectional 3 month and 15 month follow-up | Global rating of change scale, -5= much worse, 0= unchanged, 5=much better/restored |
| Satisfaction with the caregiver visits in the study | Cross-sectional 3 month and 15 month follow-up | 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) | From the time period between baseline to 15 month follow-up | 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) | Change from baseline to 3-month follow-up in the subgroup of the RCT population | 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) | Change from baseline to 3 month, subgroup of the RCT population | 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) | after intervention fulfilled, sub-group of the RCT population, n=approximately 15 | 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) | After having at least one employee participating and fulfilled the study. | Interview with managers regarding the experience of using SWEA and the Prehabguide. A subgroup will be interviewd, Approximately n=approximately 15. |
Other
| Measure | Time frame | Description |
|---|---|---|
| Treatment outside the study | Descripton baseline, 3 month, 15 month | 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 |
| work situation | Descriptive data at baseline, 3 month and 15 month follow-up | 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 |
| Background data | Baseline | Age, sex, education, family situation, pain duration, expectations, smoking history |
| Profession | Baseline | Swedish standard for work classification |
Outcome results
None listed