UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000055477
Receipt number R000063388
Scientific Title A study to investigate the effects of resistance training combined with supplementation of functional food ingredient on skeletal muscle size and strength in young male: a randomized, double-blind, placebo controlled, parallel-group comparative study.
Date of disclosure of the study information 2025/04/01
Last modified on 2024/09/10 22:57:43

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Basic information

Public title

A study to investigate the effects of resistance training combined with supplementation of functional food ingredient on skeletal muscle size and strength in young male: a randomized, double-blind, placebo controlled, parallel-group comparative study.

Acronym

A study to investigate the effects of resistance training combined with supplementation of functional food ingredient on skeletal muscle size and strength in young male: a randomized, double-blind, placebo controlled, parallel-group comparative study.

Scientific Title

A study to investigate the effects of resistance training combined with supplementation of functional food ingredient on skeletal muscle size and strength in young male: a randomized, double-blind, placebo controlled, parallel-group comparative study.

Scientific Title:Acronym

A study to investigate the effects of resistance training combined with supplementation of functional food ingredient on skeletal muscle size and strength in young male: a randomized, double-blind, placebo controlled, parallel-group comparative study.

Region

Japan


Condition

Condition

Healthy adults

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Evaluation of the effects of resistance training combined with orally administrated funtional food ingredient on skeletal muscle mass and strength in the young male and to assess the efficacy of functional food ingredient in enhancing training effects.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Actual measurement values at end measuremnt point (8 weeks after intervention; 8w) in muscle thickness

Key secondary outcomes

1) Actual measurement values at middle measurement point (4weeks after intervention; 4w) in muscle thickness

2) Amount of change and rate of change at 4w and 8w from baseline (before intervention; 0w) in maximum skeletal muscle strength


Base

Study type

Interventional


Study design

Basic design

Parallel

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

4

Purpose of intervention

Educational,Counseling,Training

Type of intervention

Food

Interventions/Control_1

Intake of test food containing lemon myrtle extract for 8 weeks and mild-intensity resistance training for 8 weeks.

Interventions/Control_2

Intake of placebo food not containing lemon myrtle extract for 8 weeks and mild-intensity resistance training for 8 weeks.

Interventions/Control_3

Intake of test food containing lemon myrtle extract for 8 weeks and moderate-intensity resistance training for 8 weeks.

Interventions/Control_4

Intake of placebo food not containing lemon myrtle extract for 8 weeks and moderate-intensity resistance training for 8 weeks.

Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

18 years-old <=

Age-upper limit

25 years-old >

Gender

Male

Key inclusion criteria

Subjects who are over 18 years old and healthy males.

Key exclusion criteria

Subjects who are prohibited from exercising by a doctor.
Subjects who take supplements ,functional foods or medicines in order to improve of muscle.
Subjects who regularly undertake resistance training.

Target sample size

60


Research contact person

Name of lead principal investigator

1st name Shuichi
Middle name
Last name Machida

Organization

Juntendo University

Division name

Graduate School of Health and Sports Science

Zip code

270-1695

Address

1-1 Hirakagakuendai, Inzai, Chiba 270-1695, Japan

TEL

0476-98-1001

Email

machidas@juntendo.ac.jp


Public contact

Name of contact person

1st name Shuichi
Middle name
Last name Machida

Organization

Juntendo University

Division name

Graduate School of Health and Sports Science

Zip code

270-1695

Address

1-1 Hirakagakuendai, Inzai, Chiba 270-1695, Japan

TEL

0476-98-1001

Homepage URL


Email

machidas@juntendo.ac.jp


Sponsor or person

Institute

Juntendo University

Institute

Department

Personal name

Shuichi Machida


Funding Source

Organization

Keneka corporation

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

Ethics committee in Juntendo University Graduate School of Health and Sports Science

Address

1-1 Hirakagakuendai, Inzai, Chiba

Tel

0476-98-1001

Email

sc-rinri@juntendo.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

2025 Year 04 Month 01 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 06 Month 26 Day

Date of IRB


Anticipated trial start date

2024 Year 09 Month 11 Day

Last follow-up date

2024 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

2024 Year 09 Month 10 Day

Last modified on

2024 Year 09 Month 10 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000063388