Stroke Cohort Outcomes of Rehabilitation 2.1
- Conditions
- Stroke
- Registration Number
- NL-OMON24488
- Lead Sponsor
- Basalt
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 351
Inclusion Criteria
•First ever or recurrent stroke (ischemic, haemorrhagic including subarachnoidal hemorrhage)
•Age =18 years
•Written informed consent
Exclusion Criteria
•Inability to communicate in the Dutch language, due to severe aphasia or insufficient knowledge of the Dutch language.
•Inability to complete questionnaires reliably due to cognitive deficits or insufficient illness awareness.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Main endpoint of this study are the responsiveness and the interpretability of the PROMIS-10 Global Health and the smRSq in stroke patients receiving rehabilitation. We will use the Standard Set for Stroke based on the recommendation by ICHOM [8] extended with several anchor questions.
- Secondary Outcome Measures
Name Time Method Secondary endpoints of this study are the correlations between the PROMIS-10 Global Health and the smRSq -as proposed by the ICHOM- and the BI [13], the SIS hand [14], PROMIS cognition, PROMIS participation and questions concerning paid work. Furthermore, the SIS cognition and PROMIS cognition will be compared.