Stroke in Working Age and Job Accommodation in Facilitating Transition Back to Work
NCT ID: NCT06709898
Last Updated: 2025-03-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
100 participants
INTERVENTIONAL
2025-01-10
2027-06-30
Brief Summary
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* Does the cognitive job accommodation intervention affect absenteeism and presenteeism after stroke?
* Does the intervention affect work ability and perceived cognitive and emotional difficulties at work?
* Does the intervention decrease mental strain, fatigue and negative mood symptoms after return to work?
* Does the intervention affect life satisfaction among the stroke patients returning to work?
Researchers will compare the intervention group to a control group returning to work after stroke with current healthcare practices and work procedures.
Participants:
* At baseline, 6 and 12 month follow-up web-based questionnaires and cognitive tests are administered.
* At 3 month follow-up participants fill in Brain Work Questionnaire (BWQ) that measures cognitive demands and difficulties at work.
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Detailed Description
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Aims: To evaluate the effect of job accommodations after stroke on various work and health related outcomes. In addition, information about working-aged stroke patients returning to work and the practices of job accommodation is provided. In the future these results can potentially be applied also to other conditions affecting cognition.
Participants and methods: This study will recruit 18-68 year old stroke patients who are returning to work (n ≈ 100). Participants will be randomized into either a job accommodation intervention group or a control group. The study will assess the benefits of cognitive job accommodation in terms of absenteeism, presenteeism, work modifications, perceived work ability, health indicators and cognitive and emotional symptoms. Participants will be followed through web-based surveys and novel cognitive tests over a 12-month period. The study will adopt a multidisciplinary approach (ergonomics, occupational psychology, neuropsychology, and medicine) and will be based on the International Classification of Functioning, Disability, and Health (ICF) model. Cognitive job accommodation will utilize an established model, a design form, and an instructional video.
Collaborators and target organizations: The research will be conducted in collaboration with the Helsinki University Hospital Neurocenter and the Finnish Institute of Occupational Health. In addition to these organizations the study is funded by the Finnish Work Environment Fund. The target organizations include occupational health services and workplaces of stroke survivors.
Utilization of Results: The methods developed in this study can be used in future collaborations between workplaces, occupational health services, and specialized healthcare. The findings can also be applied to other conditions that cause cognitive difficulties and require job accommodation.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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Cognitive job accommodation
* In intervention neuropsychological information will be individually processed and transferred systematically from the neurological unit to occupational health service (OHS) to help design the individually tailored work modifications.
* Information of the job accommodation will be given to employers.
* Cognitive job accommodation is carried out at the workplace in cooperation between the employer, employee and OHS.
* Feedback of the cognitively challenging work traits will be given to participants after returning to work.
Cognitive job accommodation
Job accommodation focused on the cognitive aspects at work
Reference group
Employees return to work according to standard health care and workplace procedures.
No interventions assigned to this group
Interventions
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Cognitive job accommodation
Job accommodation focused on the cognitive aspects at work
Eligibility Criteria
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Inclusion Criteria
* At least mild cognitive, emotional and/or state alertness symptoms detected in neuropsychological assessment in subacute phase
* Employed when the stroke occurred and has workplace where to return
* Occupational health services (OHS) available
* Participant has agreed that clinical neuropsychologist and researcher can participate to OHS consultation regarding the job accommodation
* Adequate Finnish language ability to the questionnaires and cognitive tests
Exclusion Criteria
* Former neurological or psychiatric disorder or developmental disability affecting significantly cognition
18 Years
68 Years
ALL
No
Sponsors
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Helsinki University Central Hospital
OTHER
Finnish Work Environment Fund
OTHER
Finnish Institute of Occupational Health
OTHER
Responsible Party
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Principal Investigators
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Teemu I Paajanen, Dr
Role: PRINCIPAL_INVESTIGATOR
Finnish Institute of Occupational Health
Locations
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Helsinki University Hospital Stroke Unit
Helsinki, Uusimaa, Finland
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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4011001
Identifier Type: -
Identifier Source: org_study_id
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