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A study on the combined EEG-fNIRS assessment of the impact of VR combined with different sensory modalities of meditation on the mental wandering and topological properties of brain networks in healthy individuals

A study on the combined EEG-fNIRS assessment of the impact of VR combined with different sensory modalities of meditation on the mental wandering and topological properties of brain networks in healthy individuals

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119916
Enrollment
Unknown
Registered
2026-03-05
Start date
2026-03-07
Completion date
Unknown
Last updated
2026-03-09

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

Conditions

Mind Wandering

Interventions

Bimodal group:Combination of listening and tactile sensations with breathing meditation
Traditional group:Closed-Eyed Breathing and Concentrated Meditation
Tri-modal group:The VR breathing meditation that combines sight, hearing and touch senses

Sponsors

The Second Affiliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18 - 45 years old; 2. No prior meditation experience; 3. Healthy body, no history of neurological diseases, mental disorders, or drug abuse; 4. Normal vision and hearing, or able to perceive visual and auditory stimuli after wearing corrective devices; 5. Capable of completing VR equipment wearing, touch ball operation, EEG and fNIRS data collection, and related behavioral tasks; 6. Sign the informed consent form and voluntarily participate in this study.

Exclusion criteria

Exclusion criteria: 1. There are organic or functional diseases such as cardiovascular and cerebrovascular disorders, epilepsy, schizophrenia, anxiety disorders, and depression; 2. There is a history of head trauma, brain surgery, or intracranial metal implants (which affect EEG and fNIRS data collection); 3. Allergic to the materials of VR devices or touch balls, or experiencing obvious dizziness, nausea, etc. after wearing VR devices; 4. Have taken drugs that affect the function of the nervous system in the recent period (within 1 month); 5. Pregnant or lactating women; 6. Unable to fully cooperate with the experimental process, or the researcher determines that they are not suitable to participate in this study for other reasons.

Design outcomes

Primary

MeasureTime frame
Brain network connectivity;Brain activation analysis;Neural oscillations;

Secondary

MeasureTime frame
Accuracy rate of SART task;Accuracy rate of Flanker task;

Countries

China

Contacts

Public ContactWenzhan Tu

The Second Affiliated Hospital of Wenzhou Medical University

tuwenzhan@163.com+86 135 0664 3842

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026