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Effects on Physical Condition from Using Plasma Irradiation Equipment

Effects on Physical Condition from Using Plasma Irradiation Equipments : single blinded study - Effects on Physical Condition from Using Plasma Irradiation Equipment

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000060449
Enrollment
32
Registered
2026-01-23
Start date
2026-01-19
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

Healthy adult

Interventions

For 5 days, receive 30 minutes of plasma irradiation per day using Test Article A. For 5 days, receive 30 minutes of plasma irradiation per day using Test Article B. For 5 days, receive 30 minutes of

Sponsors

Japan Clinical Trial Association
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Subjects who frequently feel tired in daily life or experience a noticeable tendency to tire easily Subjects who feel they catch colds more easily or experience more frequent health setbacks Subjects who do not consider their sleep quality perfect or are dissatisfied with it Subjects who can maintain their daily routine prior to this trial throughout the trial period Subjects who can arrive on time and participate for 5 consecutive days Subjects able to drink the provided 1.0L of water daily Subjects meeting all of the above conditions

Exclusion criteria

Exclusion criteria: Pregnant or breastfeeding individuals Subjects currently receiving treatment or prescriptions for chronic fatigue or chronic fatigue syndrome Subjects suffering from serious illnesses Subjects undergoing treatment under a physician's supervision (e.g., hormone replacement therapy, drug therapy, exercise therapy, dietary therapy) Subjects taking supplements, functional foods, or medications that affect the immune system Subjects who plan to take or are taking supplements, functional foods, or medications that affect immunity, sleep, body fat, or skin health during the trial period Subjects with food allergies Subjects with a history of drug dependence Subjects with alcohol dependence or who are heavy smokers Subjects who wish to receive or plan to receive vaccinations within 30 days prior to the trial start date or during the trial period Subjects working night shifts or rotating day-night shifts Subjects who have participated in another clinical trial within the past month or plan to participate during this trial period Other individuals deemed inappropriate by the responsible physician

Design outcomes

Primary

MeasureTime frame
Saliva test, questionnaire

Secondary

MeasureTime frame
blood flow/blood pressure/pulse measurement, body temperature

Countries

Japan

Contacts

Public ContactTakeshi Kaneko

Japan Clinical Trial Association N.A.

info@yakujihou.org0364574666

Outcome results

None listed

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