Objectives: 1) To describe the incidence and severity of cognitive impairments in patients with glioma and meningiomas before, and 3 and 12 months after surgical treatment. 2) To develop models based on presurgical sociodemographic, clinical…
ID
Bron
Aandoening
Primary brain tumor; glioma; meningioma; neurosurgery; objective cognitive functioning; cognitive deficits; neuropsychological impairment
Primaire hersentumor; gliomen; meningeomen; hersenoperatie/neurochirurgie; gezonde controles, objectief cognitief functioneren, cognitieve stoornissen
Ondersteuning
Tilburg University
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Changes in objective cognitive functioning from pre-surgery to post-surgery, as measured with a computerized neuropsychological test battery, CNS Vital Signs.
Achtergrond van het onderzoek
Deficits in cognitive functions are common in patients with primary brain tumors. These cognitive deficits can be very subtle, and easily go undetected on routine clinical examination. However, they are often very disruptive for a person’s quality of life, preventing return to a normal social and professional life.
Preservation of cognitive functioning is an important outcome measure in glioma surgery, and essential for quality of life. At present, unfortunately, it is largely unknown how surgery affects cognition. A better understanding of the variables that predict the impact of surgery on cognition is of significant importance not only to patients and their families, but also to neurosurgeons. It provides neurosurgeons with evidence-based information about possible individual risk of surgery which will steer clinical decision making and enables to inform patients better about the consequences of surgery on long-term cognitive functioning.
Doel van het onderzoek
Objectives:
1) To describe the incidence and severity of cognitive impairments in patients with glioma and meningiomas before, and 3 and 12 months after surgical treatment.
2) To develop models based on presurgical sociodemographic, clinical, imaging, and (neuro)psychological variables that predict cognitive functioning one year after surgery.
3) To increase knowledge on fatigue, work status, work limitations, and community integration, and their relationship with cognition (over time) in order to improve care for patients with primary brain tumors.
Onderzoeksopzet
Patients will complete preoperative (i.e., at the day of hospitalization one day before surgery) neuropsychological tests and questionnaires and will be followed up at 3 and 12 months after surgery. Healthy controls will be tested at the same time points.
Onderzoeksproduct en/of interventie
n/a
Publiek
Karin Gehring
PO Box 90153
Tilburg 5000 LE
The Netherlands
phone: +31 13 466 2408
e-mail: k.gehring@uvt.nl
Wetenschappelijk
Karin Gehring
PO Box 90153
Tilburg 5000 LE
The Netherlands
phone: +31 13 466 2408
e-mail: k.gehring@uvt.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Adult patients with supratentorial gliomas and meningiomas undergoing resective surgery in the St. Elisabeth Hospital, Tilburg. Eligible subjects for the control group (recruited from the general population and matched for age, gender and educational level) should be in good health, with no current or past psychiatric, neurologic, or cognitive disorder, and medication-use that interferes with cognitive function.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Patients and Dutch control subjects will be excluded if 1) they lack of basic proficiency in Dutch, 2) they have an IQ below 85 or low cognitive skills, 3) their Karnovsky Performance Scale is under 60, 4) they are completely unfamiliair with the use of computers, 5) they have an additional (history of) significant neurological or psychiatric disorder, 6) there is a surgery related complication (morbidity or mortality).
Opzet
Deelname
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Andere (mogelijk minder actuele) registraties in dit register
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In overige registers
Register | ID |
---|---|
NTR-new | NL5063 |
NTR-old | NTR5194 |
Ander register | ZonMw Projectnumber; protocol ID MEC : 842003007; NL41351.008.12 |