Skip to content

A clinical study to evaluate the effects of informing of the wall material on fatigue and fatigue sensation

A clinical study to evaluate the effects of informing of the wall material on fatigue and fatigue sensation - A clinical study to evaluate the effects of informing of the wall material on fatigue and fatigue sensation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000039615
Enrollment
112
Registered
2021-03-25
Start date
2020-02-29
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 volunteers

Interventions

Informing as wood in case of wood Informing as woodgrain sheet in case of wood Informing as wood in case of woodgrain sheet Informing as woodgrain sheet in case of woodgrain sheet

Sponsors

Soiken Inc.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Males and Females whose age of 20 years or more and less than 65 years 2)Subjects receiving a sufficient briefing of the objective and content of the present study, fully understanding and agreeing to voluntary participate in the study and being able to personally sign a written informed consent

Exclusion criteria

Exclusion criteria: 1)Subjects receiving a medical treatment for serious renal, hepatic, cardio-vascular, respiratory, endocrine or metabolic disorders or having a medical history of these disorders 2)Subjects having the chronic fatigue syndrome (CFS), or subjects deemed to have severe fatigue like idiopathic chronic fatigue by the investigator 3)Subjects who take regularly pharmaceuticals or quasi-drugs which having the efficacy for recovery from fatigue or nutrient replenishment in case of physical fatigue 4)Subjects who take regularly Foods with Function Claims labeled the effect of attenuating fatigue sensation 5)Subjects who are currently taking part in another clinical study 6)Subjects who are pregnant or lactating, or intending to become pregnant during the study 7)Subjects deemed unsuitable by the investigator

Design outcomes

Primary

MeasureTime frame
Work performance evaluation [ATMT (ABC task), ATMT (Part B)]

Secondary

MeasureTime frame
VAS (fatigue sensation, sleepiness, motivation and concentration), Jikaku-sho shirabe, autonomic nervous function evaluation

Countries

Japan

Contacts

Public ContactTomohiro Sugino

Soiken Inc. R&D Division

sugino@soiken.com06-6871-8888

Outcome results

None listed

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