UMIN-CTR Clinical Trial

Basic information
Public title	A clinical study to evaluate the effects of informing of the wall material on fatigue and fatigue sensation
Acronym	A clinical study to evaluate the effects of informing of the wall material on fatigue and fatigue sensation
Scientific Title	A clinical study to evaluate the effects of informing of the wall material on fatigue and fatigue sensation
Scientific Title:Acronym	A clinical study to evaluate the effects of informing of the wall material on fatigue and fatigue sensation
Region	Japan

Condition
Condition	Healthy volunteers
Classification by specialty	Not applicable
Classification by malignancy	Others
Genomic information	NO

Objectives
Narrative objectives1	To investigate the effects of informing of the wall material on fatigue and fatigue sensation
Basic objectives2	Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes	Work performance evaluation [ATMT (ABC task), ATMT (Part B)]
Key secondary outcomes	VAS (fatigue sensation, sleepiness, motivation and concentration), Jikaku-sho shirabe, autonomic nervous function evaluation

Base
Study type	Interventional

Study design
Basic design	Parallel
Randomization	Randomized
Randomization unit	Individual
Blinding	Open -no one is blinded
Control	Placebo
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment

Intervention
No. of arms	4
Purpose of intervention	Educational,Counseling,Training
Type of intervention	Other
Interventions/Control_1	Informing as wood in case of wood
Interventions/Control_2	Informing as woodgrain sheet in case of wood
Interventions/Control_3	Informing as wood in case of woodgrain sheet
Interventions/Control_4	Informing as woodgrain sheet in case of woodgrain sheet
Interventions/Control_5
Interventions/Control_6
Interventions/Control_7
Interventions/Control_8
Interventions/Control_9
Interventions/Control_10

Eligibility
Age-lower limit	20 years-old <=
Age-upper limit	65 years-old >
Gender	Male and Female
Key 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
Key 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
Target sample size	112

Research contact person
Name of lead principal investigator	1st name Kenji Middle name Last name Kariya
Organization	Sumitomo Forestry Co., Ltd.
Division name	Tukuba Research Institute, Wood Innovation Group
Zip code	300-2646
Address	3-2, Midorigahara, Tsukuba-shi, Ibaraki
TEL	029-847-0150
Email	KARIYA_kenji@star.sfc.co.jp

Public contact
Name of contact person	1st name Tomohiro Middle name Last name Sugino
Organization	Soiken Inc.
Division name	R&D Division
Zip code	560-0082
Address	Senri Life Science Center 13F, 1-4-2, Shinsenre-higashimachi, Toyonaka-shi, Osaka
TEL	06-6871-8888
Homepage URL
Email	sugino@soiken.com

Sponsor
Institute	Soiken Inc.
Institute
Department

Funding Source
Organization	Sumitomo Forestry Co., Ltd.
Organization
Division
Category of Funding Organization	Profit organization
Nationality of Funding Organization

Other related organizations
Co-sponsor
Name of secondary funder(s)

IRB Contact (For public release)
Organization	IRB of Fukuda Clinic
Address	Shin-Osaka Brick Building 2F, 1-6- 1, Miyahara, Yodogawa-ku, Osaka
Tel	06-6398-0203
Email	fukudaclinicIRB@gmail.com

Secondary IDs
Secondary IDs	NO
Study ID_1
Org. issuing International ID_1
Study ID_2
Org. issuing International ID_2
IND to MHLW

Institutions
Institutions

Other administrative information
Date of disclosure of the study information	2021 Year 03 Month 25 Day

Related information
URL releasing protocol
Publication of results	Unpublished

Result
URL related to results and publications
Number of participants that the trial has enrolled
Results
Results date posted
Results Delayed
Results Delay Reason
Date of the first journal publication of results
Baseline Characteristics
Participant flow
Adverse events
Outcome measures
Plan to share IPD
IPD sharing Plan description

Progress
Recruitment status	Completed
Date of protocol fixation	2020 Year 02 Month 15 Day
Date of IRB	2020 Year 02 Month 15 Day
Anticipated trial start date	2020 Year 02 Month 29 Day
Last follow-up date	2020 Year 03 Month 25 Day
Date of closure to data entry
Date trial data considered complete
Date analysis concluded

Other
Other related information

Management information
Registered date	2020 Year 02 Month 27 Day
Last modified on	2022 Year 08 Month 31 Day

Link to view the page
URL(English)	https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000045167