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Subarachnoid haemorrhage (SAH): brain injury, cognition and behaviour.

Subarachnoid haemorrhage (SAH): brain damage, cognitive and behavioral functioning as predictors of recovery.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON22031
Enrollment
150
Registered
2019-06-17
Start date
2019-07-01
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

Subarachnoid haemorrhage

Interventions

None listed

Sponsors

Catharina Heerdt foundation
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. A SAH patient, the diagnosis being based on clinical features in combination with CT angiography (CTA) or digital subtraction angiography (DSA). 2. The patient must be able to understand the instructions of the neuropsychological assessment and be mentally and physically able to undergo the research activities; this will be assessed in a consultation between the treating doctor (neurosurgeon) and researcher (neuropsychologist). 3. Sufficient knowledge of the Dutch language. 4. Age 18 or older

Exclusion criteria

Exclusion criteria: A limited physical and/or cognitive condition which makes it impossible for patients to undergo the neuropsychological assessment and MRI.

Design outcomes

Primary

MeasureTime frame
The primary outcome measure consists of the score on the Impact on Participation and Autonomy (IPA) (Cardol, 2005) questionnaire 1 year after SAH.

Secondary

MeasureTime frame
- The score on the IPA 2 years after SAH; - The score on the mRS 1 and 2 years after SAH; - Performance on neuropsychological tests (intelligence, memory, attention, mental speed, language, visuoconstruction skills, executive functions and social cognition); - Scores on questionnaires (complaints, fatigue, anxiety/depression, stress, coping, personality, behavior, quality of life) - Neuro-imaging outcomes (RS-fMRI, DWI, VBM)

Contacts

Public ContactLS Jorna

University Medical Center Groningen

l.s.jorna@umcg.nl0652129401

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)