UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000055523
Receipt number R000063447
Scientific Title A study of whether medium-chain fatty acids (8:0) are effective at breakfast or dinner.
Date of disclosure of the study information 2024/09/24
Last modified on 2024/09/18 16:59:33

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Basic information

Public title

A study of whether medium-chain fatty acids (8:0) are effective at breakfast or dinner.

Acronym

Influence of medium-chain fatty acid intake time on muscle function and memory.

Scientific Title

A study of whether medium-chain fatty acids (8:0) are effective at breakfast or dinner.

Scientific Title:Acronym

Influence of medium-chain fatty acid intake time on muscle function and memory.

Region

Japan


Condition

Condition

Nomal

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To investigate whether the duration of intake of medium-chain fatty acids affects the improvement of muscle strength and memory in healthy subjects.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Body composition, Physical ability, Concentration and memory tests

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -but assessor(s) are blinded

Control

Placebo

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Food

Interventions/Control_1

The first group is the "breakfast group" in which 18g of medium-chain fatty acids(8:0) is taken after breakfast for one month.

Interventions/Control_2

The second group is the "dinner group" in which 18g of medium-chain fatty acids(8:0) is taken at dinner for one month.

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

25 years-old >=

Gender

Male and Female

Key inclusion criteria

Healthy people between 20 and 25 years old

Key exclusion criteria

(1)Subjects with type 1 diabetes, serious heart disease, liver disease, renal disease, blood disease, etc.
(2)Persons with a BMI of 25.0 kg/m2 or more.
(3)Subjects with applicable food allergies.

Target sample size

18


Research contact person

Name of lead principal investigator

1st name Sakiko
Middle name
Last name Abe

Organization

Tezukayama University

Division name

Faculty of Contemporary Life Studies, Department of Food and Nutrition

Zip code

631-8585

Address

Gakuenminami 3-1-3, nara-shi, nara-ken

TEL

0742414742

Email

sa-abe@tezukayama-u.ac.jp


Public contact

Name of contact person

1st name Sakiko
Middle name
Last name Abe

Organization

Tezukayama University

Division name

Faculty of Contemporary Life Studies, Department of Food and Nutrition

Zip code

631-8585

Address

Gakuenminami 3-1-3, nara-shi, nara-ken

TEL

0742414742

Homepage URL


Email

sa-abe@tezukayama-u.ac.jp


Sponsor or person

Institute

Tezukayama University

Institute

Department

Personal name



Funding Source

Organization

Tezukayama University

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Tezukayama University

Address

Gakuenminami 3-1-3, nara-shi, nara-ken

Tel

0742414742

Email

sa-abe@tezukayama-u.ac.jp


Secondary IDs

Secondary IDs

YES

Study ID_1

06-26

Org. issuing International ID_1

Tezukayama University Research Ethics Committee

Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2024 Year 09 Month 24 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

Preinitiation

Date of protocol fixation

2024 Year 05 Month 23 Day

Date of IRB

2024 Year 07 Month 11 Day

Anticipated trial start date

2024 Year 09 Month 17 Day

Last follow-up date

2025 Year 03 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

2024 Year 09 Month 17 Day

Last modified on

2024 Year 09 Month 18 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000063447