UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000038533
Receipt number R000043916
Scientific Title Effect of supplements containing functional jelly on adult woman
Date of disclosure of the study information 2020/12/13
Last modified on 2022/02/22 12:36:37

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Basic information

Public title

Effect of supplements containing functional jelly on adult woman

Acronym

Effect of functional jelly clinical trial

Scientific Title

Effect of supplements containing functional jelly on adult woman

Scientific Title:Acronym

Effect of functional jelly clinical trial

Region

Japan


Condition

Condition

Adult woman

Classification by specialty

Not applicable Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Effect of supplements containing functional jelly on adult woman

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2


Developmental phase

Not applicable


Assessment

Primary outcomes

POMS2 short virsion
SRS-18(Stress Response Scale-18)
OSA sleep inventory MA version

Key secondary outcomes

Skin quality measurement
CFS(Chalder Fatigue Scale)
Visual Analogue Scale


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Placebo

Stratification

NO

Dynamic allocation


Institution consideration


Blocking

YES

Concealment



Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Food

Interventions/Control_1

To intake supplements functional jelly 3 pack/day for 4 weeks.

Interventions/Control_2

To intake placebo supplement 3 pack / day for 4 weeks.

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

30 years-old <=

Age-upper limit

51 years-old >=

Gender

Female

Key inclusion criteria

(1) persons who is generally judged as healthy
(2) Persons who can give voluntary written consent to participate in the present trial

Key exclusion criteria

(1) persons who have any dietary supplements, quasi drugs or medicines which cause same or similar efficacy with the effect evaluated in this study
(2) persons who have changed their habitats to take supplements within past 4 weeks.
(3) Persons who work in night shift or in day and night shift
(4) persons who have been treated their illness or prevention in a clinic at their informed consent
(5) persons with their medical histories as follows: serious diseases of sugar metabolism, lipid metabolism, hepatic function, renal function, heart, circulatory, respiratory, endocrine system, immune system, or mental illness of the nervous system
(6) persons with the medical histories of alcoholism or drug dependence
(7) persons who might be developed allergic reaction to foods.
(8) Persons who are pregnant, breast-feeding, or hope to be pregnant during the study period
(9) persons who had always participated in or will participate in any other clinical trial (to use foods/medicine/quasi medicine/medical device)
(10) persons who will not be judged suitable to the participants by the investigator.

Target sample size

30


Research contact person

Name of lead principal investigator

1st name Kuniyoshi
Middle name
Last name Shimizu

Organization

Faculty of Agriculture, Kyushu University

Division name

Laboratory of Systematic Forest and Forest Products Science

Zip code

812-8582

Address

744 Motooka, Nishi-ku, Fukuoka, Fukuoka, JAPAN

TEL

092-802-4673

Email

shimizu@agr.kyushu-u.ac.jp


Public contact

Name of contact person

1st name Kuniyoshi
Middle name
Last name Shimizu

Organization

Faculty of Agriculture, Kyushu University

Division name

Laboratory of Systematic Forest and Forest Products Science

Zip code

812-8582

Address

744 Motooka, Nishi-ku, Fukuoka, Fukuoka, JAPAN

TEL

092-802-4673

Homepage URL


Email

shimizu@agr.kyushu-u.ac.jp


Sponsor or person

Institute

Faculty of Agriculture, Kyushu University

Institute

Department

Personal name



Funding Source

Organization

Shinryo Co.,Ltd.

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor

User Life Science Company, Limited

Name of secondary funder(s)



IRB Contact (For public release)

Organization

Kindai University Faculty of Humanity-Oriented Science and Engineering Ethics Committee

Address

11-6 Kayanomori, Iizuka city, Fukuoka 820-8555, JAPAN

Tel

0948-22-5655

Email

ohnuki@fuk.kindai.ac.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 12 Month 13 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

2019 Year 10 Month 31 Day

Date of IRB

2019 Year 03 Month 04 Day

Anticipated trial start date

2019 Year 11 Month 11 Day

Last follow-up date

2019 Year 12 Month 13 Day

Date of closure to data entry

2019 Year 12 Month 28 Day

Date trial data considered complete

2020 Year 01 Month 03 Day

Date analysis concluded

2020 Year 01 Month 31 Day


Other

Other related information



Management information

Registered date

2019 Year 11 Month 10 Day

Last modified on

2022 Year 02 Month 22 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000043916


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name