This is an interventional neuroimaging study that will examine whether fMRI neurofeedback can shift language network activity away from regions affected by glioma prior to surgery.
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Number of participants enrolled to assess feasibility
Timeframe: up to 6 months
Number of participants completing all study visits to assess feasibility
Timeframe: From initial neurosurgical evaluation to scheduled tumor resection, 7-10 days
Number of device-related adverse events to assess safety
Timeframe: From initial neurosurgical evaluation to scheduled tumor resection, 7-10 days
Mean score Patient Experience Questionnaire (PEQ) to assess acceptability
Timeframe: Post surgery at 10 days