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A study to evaluate the effects of office environments on worker fatigue

A study to evaluate the effects of office environments on worker fatigue - A study to evaluate the effects of office environments on worker fatigue

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000043372
Enrollment
12
Registered
2021-12-03
Start date
2020-11-18
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

5 minute rest four times per one hour mental load 20 minute rest once after four hour mental load

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 with 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 receive regularly treatment for fatigue recovery (aromatherapy, reflexology, massage, etc.) or will receive it during study period 4) Subjects who take regularly pharmaceuticals or quasi-drugs which having the efficacy for recovery from fatigue or nutrient replenishment in case of physical fatigue 5) Subjects who take regularly Foods with Function Claims labeled the effect of attenuating fatigue sensation 6) Subjects who have the event which is much different from daily life during study period (house-moving, examination, etc.) 7) Subjects who are pregnant or lactating, or intending to become pregnant during the study 8) Subjects who are currently taking part in another clinical study 9) Subjects deemed unsuitable by the investigator

Design outcomes

Primary

MeasureTime frame
work performance evaluation

Secondary

MeasureTime frame
VAS, autonomic nervous function evaluation, urinalysis

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