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Cognitive Function and Health-related Quality of Life After Neuro-intensive Care (COGNI)

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Rigshospitalet

Status

Withdrawn

Conditions

Delirium
Post-traumatic Amnesia
Cognitive Dysfunction
Acute Brain Injury
Health-related Quality of Life
Sepsis

Treatments

Behavioral: no intervention

Study type

Observational

Funder types

Other

Identifiers

NCT04881097
NNF 20OC0064760

Details and patient eligibility

About

The study will provide information on cognitive impairment and Health related quality of life in patients surviving 12 months after acute brain injury, generate a hypothesis of useful variables to predict cognitive impairment or low levels of HRQoL, and potentially inform interventions for the prevention and treatment of cognitive impairment following neuro-ICU stay.

Full description

The aim is to 1) measure the frequency and extent of cognitive impairment after acute brain injury at six and 12-months after neuro-Intensive care unit (ICU) admission 2) explore the association between cognitive impairment at six and 12 months after ICU admission with the following potential risk factors: duration of ICU delirium (days), duration of sepsis (days), duration of post traumatic amnesia (days) and the severity of brain injury (initial Glasgow Coma Scale , 3) describe Health related quality of life, functional disability and frailty at six and 12 after ICU admission and 4) explore the association between the functional disability, frailty and health-related quality of life at 12 months after ICU admission

Sex

All

Ages

18 to 110 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Traumatic brain injury
  • Spontaneous intracranial hemorrhage
  • Ischemic stroke
  • An anticipated stay in the neuro-ICU for 48 hours or longer.

Exclusion criteria

  • Persistent coma defined as Richmond Agitation-Sedation Scale (RASS) -5 to -3 throughout the neuro-ICU stay
  • Congenital brain injury
  • Suspected pre-existing Cognitive impairment (Informant Questionnaire on cognitive decline in the elderly (IQCODE): 3.3 or more) (regardless of cause)
  • Permanent residence outside Denmark
  • Inability to communicate in Danish

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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