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Recruiting NCT07488780

NCT07488780 Language Network Prehab Via fMRI Neurofeedback

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Clinical Trial Summary
NCT ID NCT07488780
Status Recruiting
Phase —
Sponsor Yale University
Condition Glioma
Study Type INTERVENTIONAL
Enrollment 4 participants
Start Date 2026-08-01
Primary Completion 2026-12

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
fMRI

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 4 participants in total. It began in 2026-08-01 with a primary completion date of 2026-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: * Provision of signed and dated informed consent form * Stated willingness to comply with all study procedures and availability for the duration of the study * Diagnosis of WHO grade II-III glioma involving eloquent language cortex * Scheduled for surgical resection * MRI-compatible * Ability to perform the simple language tasks required for fMRI and neurofeedback * Residence within 2 hours of Yale MRRC and ability and willingness to make multiple visits for study participation Exclusion Criteria: * Severe baseline aphasia precluding task performance * Contraindications to MRI * Significant cognitive/psychiatric comorbidity limiting compliance * Concurrent enrollment in other interventional trials * Claustrophobia of a degree that they cannot comfortably be scanned * Inability or unwillingness to understand or follow the instructions * Pregnancy or possible pregnancy

Contact & Investigator

Central Contact

Luca Pasquini, MD, PhD

✉ luca.pasquini@yale.edu

📞 203-688-2433

Principal Investigator

Luca Pasquini, MD, PhD

PRINCIPAL INVESTIGATOR

Yale School of Medicin

Frequently Asked Questions

Who can join the NCT07488780 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Glioma. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07488780 currently recruiting?

Yes, NCT07488780 is actively recruiting participants. Contact the research team at luca.pasquini@yale.edu for enrollment information.

Where is the NCT07488780 trial being conducted?

This trial is being conducted at New Haven, United States.

Who is sponsoring the NCT07488780 clinical trial?

NCT07488780 is sponsored by Yale University. The principal investigator is Luca Pasquini, MD, PhD at Yale School of Medicin. The trial plans to enroll 4 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology