Skip to content

PROWORK: promoting a sustainable and healthy return to work toolkit for employers and their employees

PROWORK - PROmoting a sustainable return to Work: Randomised controlled pilot study assessing a Return to Work toolkit and support for line managers and their employees on long-term sick leave

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN90032009
Enrollment
60
Registered
2020-12-15
Start date
2021-01-11
Completion date
Unknown
Last updated
2025-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Reducing long-term sick leave in employees with a common mental health condition as a main condition or alongside another condition Mental and Behavioural Disorders

Interventions

A cluster randomised controlled trial with large, medium and small employer organisations with the unit of randomisation being at the level of each organisation - The intervention arm will receive a m

Sponsors

Loughborough University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Employee: 1. To have been on sick leave for at least eight days and less than six weeks (42 days)

Exclusion criteria

Exclusion criteria: Employee: 1. Under 18 years of age 2. On sick leave with a psychotic episode such as schizophrenia, or with substance abuse 3. On sick leave whilst under formal investigation for misconduct or in the formal process of disciplinary action 4. On sick leave being diagnosed with cancer and signed off work for at least 6 months 5. On sick leave due to a neurological condition (e.g. multiple sclerosis, Parkinson's disease, dementia)

Design outcomes

Primary

MeasureTime frame
1. Feasibility outcome: quantitative data describing recruitment (types of organisations participating, number of employees on long-term sick leave eligible to take part, number of employees who consent to take part, number of line managers who consent to take part), intervention (e.g. number of participants completing the steps in the online toolkits, number of times each section of the toolkit is used and attrition, number of health coaching sessions received, online training viewed and completed) gathered using study logs and predesigned forms. The forms to capture the specific data will be unique to this study and developed for its purpose. This data will be captured at baseline, and then each month up to month 6 2. Number of days taken until first day of return to work (partial or full return) using organisational records and self-report. Data collected monthly (organisational records) and at 3 months and 6 months (self-report)

Secondary

MeasureTime frame
1. Depression measured using the PHQ-9 at baseline, 3 months and six months 2. Anxiety measured using GAD-7 at baseline, 3 months and six months 3. Return to work measured by intentions to return to work scale, return-to-work self-efficacy scale and the readiness to return to work measured at baseline, 3 months and six months 4. workplace support and communication and support measured by six items developed by the research team at baseline, 3 months and six months 5. Work outcomes measured by the work productivity and activity impairment questionnaire at baseline, 3 months and six months 6. Quality of life measured by EQ5D-5L measured at baseline, 3 months and six months 7. demographic questions will be asked at baseline, 8. Use of health resources will be asked at baseline, 3 months and six months 9. Process evaluation interviews (experiences of participants, engagement with the intervention, barriers and facilitators) will take place at one time point (at 6 months for employees and line managers and at 9-12 months for employers)

Countries

England, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 14, 2026