Pain-at-Work Toolkit (Definitive Trial)

Background Chronic pain affects 28 million adults in the UK, significantly impacting their ability to be productive at work, feel fulfilled at work and/or remain in the active workforce. However, most people living with chronic pain cannot access work-related support from healthcare services, and the majority of employers do not routinely provide it. The Pain-at-Work Toolkit is a web-based resource that could help to reduce unfair differences in working lives for people with chronic pain, and positively impact their health and wellbeing, enhancing their productivity in the wider community. Co-created with people who live with pain, healthcare professionals and employers, this toolkit provides education and self-management advice to help people with chronic pain stay in, and thrive, at work.

The investigators tested the Pain-at-Work Toolkit in a preliminary trial in England ('feasibility trial' NCT05838677) . This showed that the Pain-at-Work Toolkit can be a very helpful support tool in the workplace for those living with chronic pain. The investigators recruited 18 organisations and 380 employees (50% and 217% more than expected, respectively), demonstrating that this toolkit meets a gap in employer provisions. Employees who received access to the toolkit valued its content and engaged with it without technical issues. Workers told investigators that their ability to work had improved after 6 months but these results need to be confirmed in a larger trial. Employers told investigators that they valued being able to offer it to their staff. The investigators are now updating the toolkit content to ensure it is relevant to employees across the UK.

The next step is to carry out a larger UK-wide study ('definitive trial'). The aim is to find out whether The Pain-at-Work Toolkit helps people to feel more able and confident at work, take fewer sick days, and be productive at work, and whether it provides good value for money.

The investigators will recruit at least 30 different organisations from across UK. These organisations will be randomly placed into one of two groups: one will access and use the Pain-at-Work Toolkit (the intervention group), and the other will continue as usual (the control group), to compare results fairly. A Pain-at-Work Manager Toolkit will be made available to line managers of organisations in the intervention group.

Over 600 employees will be recruited from these organisations. They will all be invited to complete online questionnaires at three time points: at recruitment, 3 months, and 6 months. The investigators will ask about their health and wellbeing, and factors relating to work, such as work ability, self-efficacy (confidence), sickness absence, work productivity, and intentions to leave.

This larger trial will include an 'implementation study'. This will involve conducting interviews with up to 60 people who have taken part in the trial and other stakeholders (such as employer representatives, line managers, HR or occupational health specialists, policymakers, professional bodies). The findings will shape our plans to make the Pain-at-Work Toolkit available widely to all workers with pain in the future.

Aims The aim of this study is to conduct a definitive cluster-randomised controlled trial, with a built-in process and implementation evaluation, to assess the effectiveness and cost-effectiveness of the Pain at Work Toolkit for improving work ability in working-age adults with chronic pain across a range of UK workplaces.

* To determine the effectiveness of the Pain-at-Work Toolkit for improving work ability in working-age adults with chronic pain * To determine intervention fidelity. * To explore the relationship between implementation fidelity and outcomes. * To understand the barriers and facilitators to successful implementation and rollout. * To generate strategies for future implementation, maintenance, and scalability.

Protocol/ Method

The study consists of 3 work packages:

* Effectiveness trial (WP1), * Health economic evaluation (WP2), * Process and implementation evaluation (WP3).

Setting is community, comprised of employment settings in different sectors (public, private, third) in UK, varying in size (small:10-49 workers; medium: 50-249 workers; large: \>250 workers).

Sample size estimate: The aim is to recruit a minimum of 30 worksites ("clusters"), approximately 15 per arm. Up to 685 participants ("employees") will be recruited from these clusters.

Up to 60 participants (employees and stakeholders) will be invited to take part in the interview study. In the case of intervention employees, this will be after the 6-month survey has been completed. Stakeholders may be interviewed at any time during the study duration, but if they are from the intervention organisation, it is likely this will be after the employees have completed their 6-month survey.

Interviews will ascertain participants' views about the Pain-at-Work Toolkit, trial processes and outcome measures, and any perceived changes in individual or organisational outcomes.

Organisations are randomised to either i) active control group (SAU: support as usual), or ii) SAU plus Pain-at-Work Toolkit and Pain-at-Work Manager's Toolkit.

• Job stressfulness [Срок оценки: To assess change between time 0 (baseline), time 1 (3 months) and time 2 (6 months).]
• Turnover intentions [Срок оценки: To assess change between time 0 (baseline), time 1 (3 months) and time 2 (6 months).]
• Depression [Срок оценки: To assess change between time 0 (baseline), time 1 (3 months) and time 2 (6 months).]
• Anxiety [Срок оценки: To assess change between time 0 (baseline), time 1 (3 months) and time 2 (6 months).]
• Health-related quality of life [Срок оценки: To assess change between time 0 (baseline), time 1 (3 months) and time 2 (6 months).]
• Health-related quality of life VAS [Срок оценки: To assess change between time 0 (baseline), time 1 (3 months) and time 2 (6months).]
• Impairments in work and activities [Срок оценки: To assess change between time 0 (baseline), time 1 (3 months) and time 2 (6 months).]
• Health resource use questionnaire [Срок оценки: Cumulative health resource use at time 0 (baseline), time 1 (3 months), time 2 (6 months).]
• Social support at work [Срок оценки: To assess change between time 0 (baseline), time 1 (3 months) and time 2 (6 months).]
• Work Self-Efficacy [Срок оценки: To assess change between time 0 (baseline), time 1 (3 months) and time 2 (6 months).]
• Occupational Self-Efficacy [Срок оценки: To assess change between time 0 (baseline), time 1 (3 months) and time 2 (6 months).]
• Pain severity [Срок оценки: To assess change between time 0 (baseline), time 1 (3 months) and time 2 (6 months).]