Footwear development for inductive revitalization of brain cells through IT fused technology applications stimulated by human foot's sports suitable for oriental acupunctural theory

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0001940

Enrollment

Registered

2016-06-09

Start date

2012-01-09

Completion date

Unknown

Last updated

2019-03-11

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

Conditions

None listed

Interventions

Medical Device : A total of 60 subjects (30 males, 30 females) in their 50s will be subjected to 12 sessions of low-frequency electrical stimulation (2Hz, the maximum level of stimulation that the hum

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Healthy males and females in their 50-60s. 2. Individuals who voluntarily participate in the clinical trial and sign the consent form.

Exclusion criteria

Exclusion criteria: Exclusion criteria 1. Individuals with autoimmune diseases such as asthma; 2. Individuals with skin allergies such as atopy; 3. Individuals with accompanying conditions that can affect the head, neck, and facial electromyogram (common cold, head injury, neck and jaw pain, toothache, or eye diseases); 4. Individuals who have undergone surgery within the last year or who have a serious medical history; 5. Individuals with metal prostheses inserted into their body; 6. Individuals with current medication (oriental medicine and western medicine) or who plan to take medication during clinical trials; 7. Individuals who are judged unable to maintain a sitting position at least for one hour; 8. Individuals who are unsuitable for low-frequency electric stimulation due to systemic skin disorders or an allergy to electrode paste; 9. Individuals who are judged unable to fill out the forms related to research performance; 10. Individuals with a medical history in psychiatry or with brain-related disorders; 11. Individuals who are judged unable to participate in the experiment easily due to their biorhythms (lack of sleep; drinking within 72 hours); 12. Individuals who are judged by the investigators to be unsuitable to participate in the clinical trial.

Design outcomes

Primary

Measure	Time frame
P300	—

Secondary

Measure	Time frame
slow alpha wave amplitude;slow alpha wave latency	—

Countries

Korea, Republic of

Contacts

Public ContactKwon Eui Hong

Daejeon University

Outcome results