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Quality of Life and Cognitive Functioning in Patients With Glial Tumors

Quality of Life and Cognitive Functioning as Prognostic Factor in Glial Tumours

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07416838
Enrollment
90
Registered
2026-02-18
Start date
2018-09-21
Completion date
2024-12-31
Last updated
2026-02-18

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

Conditions

Glial Tumors

Keywords

Glial Tumors

Brief summary

The aim of this study is to introduce appropriate assessment instruments and to define patients with gliomas according to cognitive functioning and quality of life. The study will evaluate cognitive functioning as a prognostic factor for survival in patients with glial tumors and will support optimization of treatment strategies to improve patients' quality of life.

Detailed description

This prospective cohort study will assess cognitive functioning and quality of life in patients with glial tumors. The objective is to determine the prognostic value of cognitive functioning on survival, establish appropriate assessment instruments, and contribute to treatment adaptation with the goal of improving quality of life in these patients.

Interventions

OTHERCognitive Functioning and Quality of Life Assessment

Assessment of cognitive functioning and quality of life in patients with glial tumors to evaluate their prognostic value and impact on survival outcomes.

Sponsors

Institute of Oncology Ljubljana
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

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

Inclusion criteria

* Adult participants (≥18 years) * Patients with histologically confirmed glial tumour * Ability to understand the study procedures and provide written informed consent * Ability to complete quality of life questionnaires and cognitive testing

Exclusion criteria

* Age \<18 years * Inability to provide informed consent * Severe cognitive impairment or clinical condition preventing completion of questionnaires and cognitive testing * Insufficient language proficiency to complete the questionnaires and neuropsychological testing

Design outcomes

Primary

MeasureTime frameDescription
Change in Quality of Life Score (EORTC QLQ-C30 and QLQ-BN20)Baseline (before treatment); 6 weeks; 3 months; 6 months; 12 monthsQuality of life will be assessed using the European Organisation for Research and Treatment of Cancer questionnaires EORTC QLQ-C30 and the brain cancer module EORTC QLQ-BN20. Scores range from 0 to 100 points. The outcome will be reported as mean change in questionnaire score (points) from baseline to each follow-up assessment.

Secondary

MeasureTime frameDescription
Change in Cognitive Function Test Performance (Neuropsychological Test Battery)Baseline (before treatment); 6 weeks; 3 months; 6 months; 12 monthsCognitive functioning will be assessed using a neuropsychological test battery evaluating multiple cognitive domains (e.g., language, memory, executive functioning). The outcome will be reported as mean change in test scores from baseline to each follow-up assessment.

Countries

Slovenia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026