Skip to main content
Clinical Trials/NCT05447858
NCT05447858WithdrawnNot Applicable

Systematic Work Environment Model Incorporating Web-based Neck-specific Exercise for Dental Staff With Neck Pain: A Prospective Randomized Controlled Study (WorkCIT)

Linkoeping University0 sitesStarted: January 9, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Withdrawn
Sponsor
Primary Endpoint
Current neck pain intensity

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Investigator, Outcomes Assessor)

Masking Description

Double (Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts 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 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

Arms & Interventions

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

Active Comparator

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.

Intervention: Neck-specific exercise (Other)

Neck-specific exercise in addition to SWEA

Experimental

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: SWEA (Other)

Outcomes

Primary Outcomes

Current neck pain intensity

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).

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 Outcomes

  • Symptom satisfaction(Change from baseline to 3 month and 15 month follow-up)
  • Exercise/ Physical activity level(Change from baseline to 3 month and 15 month follow-up)
  • Sick-leave(Change from baseline to 3 month and 15 month follow-up)
  • Health related quality of life, EQ-5D-5L(Change from baseline to 3 month and 15 month follow-up)
  • Perceived exertion at work(Change from baseline to 3 month and 15 month follow-up)
  • Risk identification at work(Change from baseline to 3 month and 15 month follow-up)
  • Work adaptation(Change from baseline to 3 month and 15 month follow-up)
  • Anxiety and depression(Change from baseline to 3 month and 15 month follow-up)
  • 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)
  • 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)
  • Intensity of pain and bothersomeness(Change from baseline to 3 month and 15 month follow-up)
  • Frequency of pain, symptoms and medications(Change from baseline to 3 month and 15 month follow-up)
  • Neck specific function(Change from baseline to 3 month and 15 month follow-up)
  • 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)
  • Effort-Reward Imbalance(Change from baseline to 3 month and 15 month follow-up)
  • Time sitting(Change from baseline to 3 month and 15 month follow-up)
  • Overall outcome(Cross-sectional 3 month and 15 month follow-up)
  • Fullfilment of treatment expectation(Change from baseline to 3 month and 15 month follow-up)
  • 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)
  • Interview with managers (Subgroup study)(After having at least one employee participating and fulfilled the study.)
  • Perceived work environment problems(Description and change from baseline to 3 month and 15 month follow-up)
  • Self-rated work situation regarding neck position at work(Description and change from baseline to 3 month and 15 month follow-up)
  • Satisfaction with the caregiver visits in the study(Cross-sectional 3 month and 15 month follow-up)
  • Interview study of employees (Sub-group study, not in the RCT)(after intervention fulfilled, sub-group of the RCT population, n=approximately 15)
  • Work environment related production loss(Description and change from baseline to 3 month and 15 month follow-up)
  • Health related quality of life, EQ thermometer(Change from baseline to 3 and 15 months)

Investigators

Sponsor
Linkoeping University
Sponsor Class
Other Gov
Responsible Party
Principal Investigator
Principal Investigator

Anneli Peolsson

Professor, PhD

Linkoeping University

Similar Trials