A novel computerised neuropsychological test battery for normal pressure hydrocephalus (NPH) has been developed. The aim is to provide the clinician with a free of charge, standardized tool, assessing the cognitive decline or improvements in the cognitive domains specific for NPH. Results from the battery indicate good reliability and validity for the computerized tests Results from the computerised battery seems promising. However, ability for the battery to detect cognitive improvements after a shunt operation remains to be tested. Study objectives 1. Improvement after shunt. The aim of this study is to evaluate the effects of shunting on neuropsychological performance in NPH patients, using a computerized battery. 2. Feasibility. The ability to complete the test battery by the intended patient group will be tested. 3. Baseline profile. Baseline scores for NPH-patients will be compared to scores of healthy individuals (from previous study).
Study Type
OBSERVATIONAL
Enrollment
80
Ålborg University Hospital
Aalborg, Denmark
NOT_YET_RECRUITINGLinköping University Hospital
Linköping, Sweden
NOT_YET_RECRUITINGUmeå University
Umeå, Sweden
RECRUITINGAkademiska sjukhuset
Uppsala, Sweden
NOT_YET_RECRUITINGNeuropsychological outcome
INPH patients, who are shunt candidates, will complete a computerized battery at two occasions: (1) hospital admission (Baseline) at most 1 month prior to surgery, and (2) 4.5 ± 1.5 months after shunt operation (Post-Shunt).
Time frame: 4.5 ± 1.5 months
Mini mental state Examination
INPH patients, who are shunt candidates, at each center will complete the Mini Mental State Examination at: (1) hospital admission (Baseline) at most 1 month prior to surgery, and (2) 4.5 ± 1.5 months after shunt operation (Post-Shunt).
Time frame: 4.5 ± 1.5 months
Feasibility
The number of patients who are able to complete individual subtests and the entire battery, will be monitored.
Time frame: 4.5 ± 1.5 months
Baseline cognitive profile compared to healthy
The baseline cognitive profile of INPH-patients will be compared to healthy individuals (from previous study).
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