UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000046676
Receipt number R000053246
Scientific Title Examination of muscle hypertrophy effect for hospital staff by implementing a professional exercise program
Date of disclosure of the study information 2022/01/19
Last modified on 2023/05/03 09:20:26

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Basic information

Public title

Examination of muscle hypertrophy effect for hospital staff by implementing a professional exercise program

Acronym

Examination of muscle hypertrophy effect for hospital staff by implementing a professional exercise program

Scientific Title

Examination of muscle hypertrophy effect for hospital staff by implementing a professional exercise program

Scientific Title:Acronym

Examination of muscle hypertrophy effect for hospital staff by implementing a professional exercise program

Region

Japan


Condition

Condition

Healthy person

Classification by specialty

Not applicable Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Verification of muscle hypertrophy effect

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Skeletal muscle mass 12 weeks after intervention

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Behavior,custom

Interventions/Control_1

Strength training and balance training for 12 weeks, 3 times a week

Interventions/Control_2

Continuation of normal life

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

65 years-old >=

Gender

Male and Female

Key inclusion criteria

Being able to carry an accelerometer during the research period
Being able to participate in all 36 training sessions

Key exclusion criteria

Non-independent walking and restricted daily life by doctors
Have an exercise habit

Target sample size

40


Research contact person

Name of lead principal investigator

1st name yasuhiro
Middle name
Last name suzuki

Organization

University of Tsukuba Hospital

Division name

Department of Rehabilitation Medicine

Zip code

305-0044

Address

2-1-1 Amakubo

TEL

0298533795

Email

minaminagasaki2007@yahoo.co.jp


Public contact

Name of contact person

1st name yasuhiro
Middle name
Last name suzuki

Organization

University of Tsukuba Hospital

Division name

Department of Rehabilitation Medicine

Zip code

305-0044

Address

2-1-1 Amakubo

TEL

0298533795

Homepage URL


Email

minaminagasaki2007@yahoo.co.jp


Sponsor or person

Institute

University of Tsukuba

Institute

Department

Personal name



Funding Source

Organization

University of Tsukuba

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

University of Tsukuba Hospital

Address

2-1-1 Amakubo

Tel

0298533795

Email

minaminagasaki2007@yahoo.co.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 01 Month 19 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

2022 Year 01 Month 26 Day

Date of IRB

2022 Year 01 Month 26 Day

Anticipated trial start date

2022 Year 01 Month 26 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



Management information

Registered date

2022 Year 01 Month 19 Day

Last modified on

2023 Year 05 Month 03 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000053246


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name