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Evaluation of the Variation Over Time of Visuospatial Deficit in Patients With Parietal Lobe Glioma

Evaluation of the Variation Over Time of Visuospatial Deficit in Patients With Parietal Lobe Glioma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07286929
Acronym
neGLIO
Enrollment
40
Registered
2025-12-16
Start date
2024-12-03
Completion date
2026-10-31
Last updated
2025-12-16

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

Conditions

Glioma, Parietal Lobe Glioma, Unilateral Spatial Neglect (USN), Visuspatial Deficit

Keywords

Visuospatial deficit, Glioma, Parietal Lobe, Neuropsychological assessment, Hemineglect

Brief summary

The goal of modern neurooncological surgery is to obtain maximum tumor resection while preserving neurological function. Parietal lobe gliomas often cause attention deficits (hemineglect) that are difficult to differentiate from other deficits. This study aims to evaluate the extent and variation over time of visuo-spatial deficits in patients undergoing surgical removal of parietal lobe gliomas. This will help characterize the cognitive profile of these patients to identify personalized treatment and rehabilitation paths.

Detailed description

This is a single-centre, prospective, cross-sectional, observational study involving 40 patients with high- and low-grade parietal lobe glioma. The study investigates the prevalence of subjects who show a performance in cognitive visuo-spatial tests below the cut-off of the normative sample. It evaluates associations with patient-reported outcome measures (ADL, IADL), clinical-demographic aspects, radiological data (MRI), and histological/molecular data. Assessments occur at screening (pre-surgery), and at follow-up visits (3-4 months and 6 months post-surgery). Neuropsychological tests include Line Bisection, Bell and Letter Cancellation, Reading test, Apple Cancellation, and Fluff test.

Interventions

None listed

Sponsors

Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients \>18 years old * Patients must understand the Italian Language * Patients with suspected parietal lobe glioma

Exclusion criteria

* Tumor site other than parietal lobe. * Patients who cannot undergo surgical resection (stereotactic/open biopsy). * Patients who received a previous chemotherapy and/or radiotherapy treatment. * Patients with a history of intracranial mass lesion or traumatic brain injury. * Patients with a history of other CNS diseases (e.g., stroke, metastasis). * Patients with diagnosis of neurodegenerative disease (i.e. Alzheimer's Disease, Frontotemporal Dementia, Parkinson's Disease, Lewy Body Dementia, Amyotrophic Lateral Sclerosis).

Design outcomes

Primary

MeasureTime frameDescription
Change in Visuospatial Deficit PrevalenceBaseline (pre-surgery), 3-4 months post-surgery, 6 months post-surgery.Prevalence of patients with a score below the cut-off in specific neuropsychological tests for visuo-spatial aspects (Line Bisection, Bell/Letter Cancellation, Apple Cancellation, Fluff Test) and the extent of change compared to baseline.

Secondary

MeasureTime frameDescription
Association with Performance StatusTime Frame: Up to 6 months post-surgery.Correlation between visuo-spatial scores and Karnofsky Performance Status (KPS).
Association with Radiological DataUp to 6 months post-surgeryCorrelation between visuo-spatial deficit scores and MRI data (FLAIR volume, T1 contrast, necrosis, localization).
Association with Clinical-Demographic DataUp to 6 months post-surgery.Correlation between visuo-spatial scores and hemispheric dominance, age, sex, and education.
Association with Histological/Molecular DataUp to 6 months post-surgery.Correlation between visuo-spatial scores and tumor grade, histological and molecular features.

Countries

Italy

Contacts

Primary ContactFrancesco Di Meco, MD
francesco.dimeco@istituto-besta.it+ 39 02.2394

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026