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NCT Number: NCT07699172

EEG-Guided Cognitive Function Preservation in Patients With Brain Tumors

Brain tumors and their surgical treatment may impair cognitive function, affecting patients' quality of life. This prospective single-arm study aims to evaluate the feasibility and clinical utility of an EEG-based neural signal decoding strategy for cognitive function preservation in patients undergoing brain tumor surgery. Participants will undergo standardized neuropsychological assessments together with preoperative, intraoperative, and postoperative electrophysiological recordings. The study will investigate whether EEG-based neural decoding can improve objective cognitive function assessment and support individualized functional preservation during brain tumor surgery.

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Key information

About this study

This is a prospective, single-center, single-arm interventional study designed to investigate an EEG-based neural signal decoding strategy for higher-order cognitive function preservation in patients undergoing brain tumor surgery.

Eligible patients with brain tumors scheduled for surgical treatment will be enrolled. Participants will receive standardized neuropsychological assessments before and after surgery. High-density EEG recordings will be acquired during different stages of the perioperative period, including task-based and resting-state paradigms when applicable. Neural signal decoding methods will be used to extract cognitive-related electrophysiological features and evaluate their association with postoperative cognitive outcomes.

The primary objective is to evaluate the feasibility of EEG-based neural signal decoding for objective cognitive assessment and functional preservation during brain tumor surgery. Secondary objectives include exploring the relationship between electrophysiological biomarkers and neuropsychological performance, evaluating perioperative cognitive changes, and providing preliminary evidence for individualized cognitive protection strategies in brain tumor patients.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 years to 75 years.
  • Patients diagnosed with brain glioma and scheduled for surgical treatment.
  • Conscious and able to understand study procedures.
  • Able to complete neuropsychological assessments.
  • Willing to participate and provide written informed consent.

Exclusion criteria

  • Severe dysfunction of major organs (heart, lung, liver, or kidney).
  • Severe psychiatric disorders or cognitive impairment.
  • Severe language impairment preventing completion of study procedures.
  • Any other condition judged by the investigator to make participation inappropriate.

Treatment and study plan

EEG-Based Neural Signal Decoding Strategy

Procedure

EEG-based neural signal decoding will be performed during the perioperative period to identify cognitive functional networks and assist individualized cognitive function preservation during brain tumor surgery.

Primary outcomes

  1. Mini-Mental State Examination (MMSE) Total Score

    Time frame: Baseline, postoperative 1 week, postoperative 1 month, and postoperative 3 months

    Cognitive function assessed using the Mini-Mental State Examination (MMSE). The total score ranges from 0 to 30, with higher scores indicate better cognitive function.

  2. Montreal Cognitive Assessment (MoCA) Total Score

    Time frame: Baseline, postoperative 1 week, postoperative 1 month, and postoperative 3 months

    Cognitive function assessed using the Montreal Cognitive Assessment (MoCA). The total score ranges from 0 to 30, with higher scores indicate better cognitive function.

Study contacts

Contact information is provided by the study sponsor or research team.

Sponsors and collaborators

Lead sponsor

Bo Wang

Other

Registry information

Official study title

A Prospective Single-Arm Study of EEG-Based Neural Signal Decoding for Cognitive Function Preservation in Patients Undergoing Brain Tumor Surgery

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Jul 13, 2026
Registry last updated
Jul 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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