UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000048769
Receipt number R000055560
Scientific Title Core body temperature, menstrual cycle, and circadian rhythm
Date of disclosure of the study information 2022/08/26
Last modified on 2023/02/27 12:19:42

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Core body temperature, menstrual cycle, and circadian rhythm

Acronym

Core body temperature, menstrual cycle, and circadian rhythm

Scientific Title

Core body temperature, menstrual cycle, and circadian rhythm

Scientific Title:Acronym

Core body temperature, menstrual cycle, and circadian rhythm

Region

Japan


Condition

Condition

menstrual disorders and circadian rhythm disorders

Classification by specialty

Obstetrics and Gynecology Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The primary aim is to test the feasibility of a study device to investigate core body temperature measured at the navel, menstrual periods, and circadian rhythm. The second aim is to examine whether the body temperature changes measured at the navel indicate circadian rhythm. The third aim is to identify factors that affect menstrual periods, sleep, or circadian rhythm.

Basic objectives2

Others

Basic objectives -Others

The feasibility study of a study device that can be used for investigating core body temperature measured at the navel, menstrual periods, and circadian rhythm.

Trial characteristics_1


Trial characteristics_2


Developmental phase

Not applicable


Assessment

Primary outcomes

The correlation between the body temperature changes measured at the navel and the melatonin curve projected by melatonin excretion.

Key secondary outcomes



Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


Interventions/Control_2


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

40 years-old >

Gender

Female

Key inclusion criteria

1) Women who are in their 20s and 30s and have periods periodically. 2) Those who consent to join a study of their own will after receiving the right and thorough information about the study.

Key exclusion criteria

1) Those who have chronic diseases such as hypertension, diabetes, or cardiac diseases. 2) Those who have a mental illness such as anorexia. 3) Those who consume oral contraceptives. 4) Those who consume sleeping pills. 5) Those who have a gynecological disease and have medical treatment. 6) Those who have a navel piercing. 7) Those who are or can be pregnant, or hope to get pregnant within three months after the consent to join the study. 8) Those who a principal investigator of this study thinks is inappropriate as a subject.

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Sayuri
Middle name
Last name Tanaka

Organization

MEDITA inc.

Division name

CEO

Zip code

103-0024

Address

7-12 Nihon-bashi Kohikicho, Green Park Nihonbashi Mitsukoshimae 1101, Chuo-ku Tokyo, Japan

TEL

050-3184-0927

Email

tanaka@medita.inc


Public contact

Name of contact person

1st name Sayuri
Middle name
Last name Tanaka

Organization

MEDITA inc.

Division name

N/A

Zip code

103-0024

Address

7-12 Nihon-bashi Kohikicho, Green Park Nihonbashi Mitsukoshimae 1101, Chuo-ku Tokyo, Japan

TEL

050-3184-0927

Homepage URL


Email

clinical_trial@medita.inc


Sponsor or person

Institute

MEDITA inc.

Institute

Department

Personal name



Funding Source

Organization

New Energy and Industrial Technology Development Organization

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Public Health Research Center

Address

1-1-7, Nishiwaseda, Shinjuku, Tokyo, Japan

Tel

03-5287-5070

Email

rinri@phrf.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

2022 Year 08 Month 26 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

No longer recruiting

Date of protocol fixation

2022 Year 08 Month 19 Day

Date of IRB

2022 Year 08 Month 19 Day

Anticipated trial start date

2022 Year 08 Month 30 Day

Last follow-up date

2023 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

This observational study asks subjects to stay at a hotel before and after their periods for measuring their body temperature at the navel, exercise and diet habits, sleep, and other vital data for approximately eight consecutive days.


Management information

Registered date

2022 Year 08 Month 26 Day

Last modified on

2023 Year 02 Month 27 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000055560


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name