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Study identifier: NCT07264387 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Predictive Factors for Return to Work After a First Stroke Treated at Clermont-Ferrand University Hospital in Puy de Dôme Between January 2020 and December 2024

Condition: Stroke  ·  Sponsor: University Hospital, Clermont-Ferrand

PhaseN/A
Planned participants140
Who can joinAll sexes, 18 Years to 64 Years
Healthy volunteersNo

About this study

Stroke is a leading cause of acquired motor disability and the second most common cause of major cognitive impairment worldwide. In France, approximately 150,000 new cases occur annually, with around 31% affecting individuals of working age, making return to work (RTW) a critical public health issue. Beyond the medical burden, stroke has profound socio-economic consequences, including loss of productivity, prolonged sick leave, part-time resumption, and the need for workplace adaptations. While RTW after stroke has been investigated, major gaps remain. No standardized recommendations exist for vocational reintegration, and predictive factors are still debated. Quantitative determinants such as stroke type, severity, functional independence, and occupational characteristics have been identified, but qualitative aspects-including self-efficacy, perceived social burden, employer relationships, and motivation-are poorly documented. Moreover, cognitive deficits are often insufficiently characterized, as screening tools such as MMSE or MoCA lack the sensitivity of comprehensive neuropsychological assessments. The impact of revascularization procedures on RTW and the ability to sustain employment after initial resumption also remain unclear. Importantly, no recent data are available in the Auvergne region, despite evolving labor policies that may influence reintegration trajectories. This observational study therefore aims to identify both quantitative and qualitative predictors of …

This description comes directly from the study's public registry record.

Talk to the study team

Lise Laclautre  ·  +33473754963  ·  promo_interne_drci@chu-clermontferrand.fr

Always discuss trial participation with your own doctor first.

Locations (2)

Clermont Ferrand University Hospital, Louise Michel siteCébazat, France, FranceRecruiting
CHU Clermont-Ferrand, Louise MichelClermont-Ferrand, FranceNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT07264387