UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000040900
Receipt number R000046700
Scientific Title Influence of far-infrared radiation mattress pad on human thermo- and sleep-wake regulations
Date of disclosure of the study information 2020/06/25
Last modified on 2023/08/29 18:13:47

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Basic information

Public title

Influence of far-infrared radiation mattress pad on human thermo- and sleep-wake regulations

Acronym

Influence of far-infrared radiation mattress pad on human thermo- and sleep-wake regulations

Scientific Title

Influence of far-infrared radiation mattress pad on human thermo- and sleep-wake regulations

Scientific Title:Acronym

Influence of far-infrared radiation mattress pad on human thermo- and sleep-wake regulations

Region

Japan


Condition

Condition

healthy human

Classification by specialty

Psychiatry Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

thermoregulation

Basic objectives2

Others

Basic objectives -Others

sleep-wake regulation

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

core body temperature, skin temperature

Key secondary outcomes

distal-proximal skin-temperature gradient, heart rate variability, sleep parameters, subjective sleepiness, mood, cold warm sensation, restlessness


Base

Study type

Interventional


Study design

Basic design

Cross-over

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Placebo

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Other

Interventions/Control_1

far-infrared mattress pad (a night of sleep)

Interventions/Control_2

sham mattress pad (a night of sleep)

Interventions/Control_3


Interventions/Control_4


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

60 years-old >

Gender

Male and Female

Key inclusion criteria

Healthy adults

Key exclusion criteria

Those who past and under treatments of chronic diseases (cardiovascular, hepatic, endocrine, neurological, and mental disorders).
Those who with alcoholism.
Those who using sleep agents.
Those who are shiftworkers or/and traveled across time zones in six months.
Those who with other inappropriate factors for participation in this study.

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Kenichi
Middle name
Last name Kuriyama

Organization

National Center of Neurology and Psychiatry

Division name

Department of Sleep-Wake Disorders, National Institute of Mental Health

Zip code

187-8553

Address

4-1-1 Ogawa-Higashi, Kodaira, Tokyo

TEL

042-346-2071

Email

kenichik@ncnp.go.jp


Public contact

Name of contact person

1st name Kenichi
Middle name
Last name Kuriyama

Organization

National Center of Neurology and Psychiatry

Division name

Department of Sleep-Wake Disorders, National Institute of Mental Health

Zip code

187-8553

Address

4-1-1 Ogawa-Higashi, Kodaira, Tokyo

TEL

042-346-2071

Homepage URL


Email

kenichik@ncnp.go.jp


Sponsor or person

Institute

National Center of Neurology and Psychiatry

Institute

Department

Personal name



Funding Source

Organization

PMC 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

Ethical Committee of National Center of Neurology and Psychiatry

Address

4-1-1 Ogawa-Higashi, Kodaira, Tokyo

Tel

042-341-2712

Email

rinri-jimu@ncnp.go.jp


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

2020 Year 06 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

18

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

2019 Year 08 Month 05 Day

Date of IRB

2019 Year 10 Month 09 Day

Anticipated trial start date

2020 Year 07 Month 01 Day

Last follow-up date

2022 Year 12 Month 31 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 06 Month 25 Day

Last modified on

2023 Year 08 Month 29 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000046700


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name