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Stroke Cohort Outcomes of Rehabilitation 2.1

Stroke Cohort Outcomes of Rehabilitation 2.1

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON24488
Enrollment
351
Registered
2021-05-21
Start date
2021-07-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Stroke

Interventions

None listed

Sponsors

Basalt
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • First ever or recurrent stroke (ischemic, haemorrhagic including subarachnoidal hemorrhage) • Age =18 years • Written informed consent

Exclusion criteria

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.

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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.

Contacts

Public ContactDaniella Oosterveer

Basalt

d.oosterveer@basaltrevalidatie.nl0715195195

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)