Skip to content

Apathy Evaluation as New outcome After Stroke (AENEAS)

Apathy Evaluation as New outcome After Stroke (AENEAS) - Apathy After Stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON35801
Enrollment
500
Registered
2011-07-21
Start date
2011-09-28
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

apathy behavioral disorder

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Stroke for which hospitalization was indicated approximately three months ago. Participation in one of two randomized controlled trials in acute stroke (ARTIS-trial, PASS-trial). National Institutes of Health Stroke Scale (NIHSS) 2-20

Exclusion criteria

Exclusion criteria: aphasia; major depression or dementia prior to stroke

Design outcomes

Primary

MeasureTime frame
Primary outcome is the effect of the interventions in the ARTIS and PASS trials on apathy 3 and 9 months after stroke.

Secondary

MeasureTime frame
Secondary outcomes are the effect of the interventions in ARTIS and PASS on depression and cognitive function 3 and 9 months after stroke. The effect of apathy, depression and cognitive impairment on functional recovery will be evaluated.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)