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Studies on how synesthesia experiences affect human physiology

Multi-omics analyses on how synesthesia experiences affect human physiology - How synesthesia experiences affect human multi-omics?

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000050381
Enrollment
30
Registered
2023-02-20
Start date
2023-02-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

None listed

Interventions

The use of Synesthesia X1 system The use of Synesthesia X1 system without vibration

Sponsors

Tohoku university
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Those who are between 20 and 65 years of age, have Asian nationality, have a BMI between 18.5 and 30.0, and weigh 40 kg or more, and have been given a full explanation of the study before enrolling in the study and have obtained written consent from the subject after understanding the details of the study.

Exclusion criteria

Exclusion criteria: Patients with the following clinically problematic diseases: Hematological diseases renal diseases endocrine disease Pulmonary disease Gastrointestinal disease Cardiovascular Diseases Liver disease Those with a history of, or currently suffering from, psychiatric or mental disorders Those with a history of serious head and spinal cord trauma, surgery, gastrointestinal tract, urinary tract bleeding, major surgery, or serious non-head trauma within the past 3 months Pregnant or lactating mothers. The Principal Investigator will confirm whether or not the above conditions apply to the applicant at the time of application by e-mail, etc., and at the time of explanation. If the applicant is not sure, the Principal Investigator will contact a licensed physician on the spot to determine whether or not the condition applies to the applicant and whether or not the applicant may participate. Other applicants who are deemed ineligible for inclusion by the Principal Investigator (e.g., those with extreme sleep disorders or excessive stress, those with symptoms such as menopausal disorders, etc.). Students and staff members affiliated with the principal investigator's or subinvestigator's laboratory, as well as students who are involved in grade approval by the principal investigator or subinvestigator, will not be eligible for inclusion in the study.

Design outcomes

Primary

MeasureTime frame
Changes in blood metabolites and soluble factors, gene expression changes in immune cells, and changes in biological signals (pre- and post-device use)

Countries

Japan

Contacts

Public ContactMayuko Yoda

Tohoku university Institute of Development, Aging and Cancer

mayuko.yoda.e8@tohoku.ac.jp022-717-8568

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026