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EEG-Guided Binaural Beat Audio to Reduce Performance-Related Stress and Improve Cognition

T

Texas Tech University Health Sciences Center

Status

Not yet enrolling

Conditions

Performance
Cognitive Performance
Cognitive Abilities
Stress

Treatments

Other: Non-binaural audio intervention
Other: EEG-guided binaural beat audio

Study type

Interventional

Funder types

Other

Identifiers

NCT07407426
IRB2025-681

Details and patient eligibility

About

Performance-related stress can impair sustained attention, inhibitory control, and memory. This randomized, double-blinded, sham-controlled parallel-arm trial evaluates whether a 30-minute EEG-guided binaural beat audio intervention reduces subjective stress/performance anxiety and improves cognition, and whether it changes task-related brain reactivity measured by fMRI. The intervention uses real-time single-electrode EEG recorded over the left prefrontal cortex to dynamically adjust binaural beat frequencies to guide the brain toward a target state; the sham condition uses non-binaural music delivered through identical headphones.

Adult music majors preparing for an upcoming concert will complete pre- and post-intervention fMRI sessions during cognitive/music tasks (Stop Signal Reaction Task, Music Reading Task, Music Memory Retrieval Task) and complete visual analog scales (VAS) assessing performance anxiety, stress, and related subjective states. The primary outcomes include fMRI task-related activity in stress-regulation regions (dlPFC, amygdala, hippocampus), behavioral inhibition indices from the stop-signal task, music memory retrieval accuracy, and VAS-reported stress/performance anxiety.

Full description

This study will test the efficacy and neurophysiologic mechanism of a novel EEG-guided binaural beat audio intervention for mitigating performance-related stress and enhancing cognition in musicians. The study is conducted at Texas Tech University (recruitment/screening/analysis) with neuroimaging and cognitive task data collection at the Texas Tech Neuroimaging Institute (TTNI).

Participants complete a single in-person visit (~3 hours) including consent and eligibility screening, task training, pre-intervention VAS and fMRI scanning, randomization to intervention or sham, a 30-minute audio session, post-intervention fMRI scanning, and post-intervention VAS.

The experimental audio intervention uses a proprietary algorithm with real-time EEG feedback from a single electrode over the left prefrontal cortex to dynamically adjust binaural beat frequencies during a 30-minute session delivered through headphones. The sham comparator uses non-binaural audio (music without interaural frequency differences) delivered identically. Participants and researchers conducting assessments are blinded to allocation.

Enrollment

32 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adults (18+ years) enrolled as undergraduate music majors at Texas Tech University
  • Currently preparing for an upcoming concert performance within the next 3 months
  • Able to read standard musical notation

Exclusion criteria

  • Subjects with contraindications to undergo MRI after being screened by the TTNI safety screening sheet - specifically, Subjects with implanted devices that are not compatible with MRI including, but not limited to cardiac pacemakers, cardiac defibrillators, aneurysm clips, carotid artery vascular clamps, implanted nerve stimulators (neuron-stimulators also called TENS or wires), bone growth or bone fusion stimulators, cochlear implants, vagus nerve stimulators, filters for blood clots (Umbrella, Greenfield, bird's nest), embolization coils (e.g. Gianturco) in the brain, ocular implants, vascular stents, medication pumps, medication patches delivering medications, implanted limbs, ventricular shunts, metal joints, rods, plates, pins, screws, nails, or clips, penile implants, or contraceptives devices including IUDs, cervical pessaries and diaphragms Subjects who have undergone cataract surgery Subjects who have shrapnel or metal in the head, eyes or skin Subjects with a history of working with metal fragments ( or have had metal removed from eyes Subjects with gunshot wounds or BB gun injury Subjects with permanent metal body piercings or jewelry that cannot be removed Subjects who use hearing aids or have braces / permanent retainers that cannot be removed temporarily for the MRI scans Subjects with large tattoos in the head and neck area Subjects with claustrophobia Subjects who are currently pregnant or suspected to be pregnant
  • Physical, medical, neurological or psychiatric impairments (including substance abuse)
  • Current use of medications that could affect cognitive performance (including beta-blockers, stimulants, anxiolytics, antidepressants, or antipsychotics)
  • History of head injury resulting in loss of consciousness/history of brain surgery
  • History of diagnosed hearing impairment or use of hearing aids
  • Current or past diagnosis of epilepsy or seizure disorders
  • Unwillingness or inability to refrain from alcohol consumption 48 hours prior to the study visit
  • Unwillingness or inability to refrain from caffeine consumption 12 hours prior to the study visit
  • Current/past history of substance abuse
  • Pregnancy or possibility of pregnancy
  • Unwillingness or inability to follow written, on-screen, and verbal instructions given by the study team

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

32 participants in 2 patient groups

EEG-guided binaural beat audio
Experimental group
Description:
30-minute session delivered via headphones; proprietary algorithm uses real-time single-electrode EEG from the left prefrontal cortex to dynamically adjust binaural beat frequencies.
Treatment:
Other: EEG-guided binaural beat audio
non-binaural audio
Sham Comparator group
Description:
30-minute session of music without frequency differences between ears (non-binaural), delivered via identical headphones; blinding maintained.
Treatment:
Other: Non-binaural audio intervention

Trial contacts and locations

1

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Central trial contact

Chathurika S Dhanasekara, MD, PhD; Chanaka N Kahathuduwa, MD, PhD

Data sourced from clinicaltrials.gov

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