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Return to Work After Stroke (RETAKE)

Early vocational rehabilitation compared with usual care for stroke survivors: an individually randomised controlled multi-centre pragmatic trial with embedded economic and process evaluations

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN12464275
Enrollment
582
Registered
2018-03-13
Start date
2018-04-01
Completion date
Unknown
Last updated
2026-04-20

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

Conditions

Stroke Circulatory System Stroke, not specified as haemorrhage or infarction

Interventions

This study will involve 760 stroke survivors (420 ESSVR plus usual care, 340 usual care alone), who are employed at stroke onset, and their carers (if applicable). Two occupational therapists from 20

Sponsors

University of Nottingham
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Age =18 years 2. Admitted to hospital with new stroke (all severities) 3. In work at stroke onset (including self-employed, paid or unpaid) 4. Willing and have capacity to provide informed consent to participate in the study 5. Have sufficient proficiency in English to contribute to the data collection required for research

Exclusion criteria

Exclusion criteria: Not intending to work

Design outcomes

Primary

MeasureTime frame
Self-reported return to work of at least 2 hours per week at 12 months post randomisation. This may be a return to a pre-stroke job or a new job. This will be recorded as a positive response to the question: ‘Are you currently in work(paid or unpaid) for at least 2 hours per week?’; Timepoint(s): 12 months post-randomisation

Secondary

MeasureTime frame
All secondary outcomes are measured at 3, 6 and 12 months: 1. Work-related outcomes: return to work with same employer, number of hours worked, number of days in work 2. Mood, assessed using the Hospital Anxiety & Depression Scale (HADS) anxiety and depression scores 3. Physical function, assessed using the Nottingham Extended Activities of Daily Living scale (NEADL) summary score 4. Social participation, assessed using the Community Integration Questionnaire (CIQ) social and productivity scores 5. Work self-efficacy, measured using a single question from the work ability index 6. Health-related quality of life, measured using the EuroQoL 5 dimension health questionnaire, 5 level (EQ-5D-5L) 7. Health and social care resource use and wider resource use (e.g. productivity, personal or carer costs): self reported A&E attendances, hospital admission/readmission, number of work accidents, overall health and social care resource use, measured using a bespoke patient completed resource use questionnaire 8. Post-stroke confidence, measured using the Confidence after Stroke Measure (CaSM) summary score Process Evaluation Intervention compliance and how the intervention is experienced and understood by providers and recipients, and the organisational implications of embedding and sustaining the intervention in preparation for wider NHS roll-out. Measured using an embedded mixed-methods process evaluation using a range of methods including observations, qualitative interviews with participants, carers, service providers and employers, non-participant observation in sites, document analysis (case records and intervention proformas) and care mapping in a random sample of cases (up to 5% of participants in both ESSVR and UC) Internal Pilot (8 Sites) Recruitment rates at 4 – 6 months post randomisation and follow-up rates after 12 months post-randomisation, to assess whether they meet the predefined progression criteria thresholds

Countries

England, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 23, 2026