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Evaluation of Psychophysiological Effects Induced by Radiant Heat Systems

Evaluation of Psychophysiological Effects Induced by Radiant Heat Systems - Evaluation of Psychophysiological Effects Induced by Radiant Heat Systems

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000052676
Enrollment
20
Registered
2024-11-05
Start date
2023-11-06
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

Male/female adults

Interventions

Staying in a room with the Radiant Heat System (ENRICH) for 15 minutes. Staying in an adjacent room with controlled temperature and humidity for 15 minutes.

Sponsors

P&C PLANNING CO., LTD.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Healthy males and females aged 20 and older. 2. Subjects who can give informed consent to partake in this research, after being provided with an explanation of the protocol detail.

Exclusion criteria

Exclusion criteria: 1. Subjects with a smoking habit. 2. Subjects who are cold-sensitive constitution (including subjects like that who feel cold on their hands and foots even in summer). 3. Subjects diagnosed with any disease and receiving drug treatments (e.g., antihypertensive drugs, antiepileptic drugs) at the time of consent. 4. Subjects who have taken or applied drugs for disease treatment in the past month (excluding cold remedies but including treatments for hay fever). 5. Subjects who underwent surgery on the measurement areas (chest, face, fingertips) within the past 6 months. 6. Subjects currently participating in another clinical trial or those who have participated in a clinical trial within the past month. 7. Subjects with issues regarding electrocardiogram measurements (e.g., dense chest hair, pacemaker users). 8. Subjects with previous and/or current medical history of serious diseases in liver, kidney, heart, lung, blood. 9. Pregnant or lactating Subjects or those with the possibility of pregnancy. 10 Subjects with dermatological conditions such as atopic dermatitis. 11 Subjects experiencing pain in the knee or discomfort when bending the knee. 12. Subjects deemed unsuitable for participation in the trial by the principal investigator.

Design outcomes

Primary

MeasureTime frame
Pupillary light reflex Skin temperature (fingertips and forehead) Electrocardiogram (ECG) Vascular age Flicker value Brain age Stress Checklist 30-item (SCL30) Visual Analog Scale (VAS) Multiple mood scale

Countries

Japan

Contacts

Public ContactAiko Ueda

P&C PLANNING CO., LTD. CEO

info@8p-ch.com092-725-6623

Outcome results

None listed

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