UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000045725
Receipt number R000052201
Scientific Title Study on the learning effects of random force control on the standing balance
Date of disclosure of the study information 2021/10/12
Last modified on 2026/04/09 19:41:45

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Basic information

Public title

Study on the learning effects of random force control on the standing balance

Acronym

Study on the learning effects of random force control on the standing balance

Scientific Title

Study on the learning effects of random force control on the standing balance

Scientific Title:Acronym

Study on the learning effects of random force control on the standing balance

Region

Japan


Condition

Condition

Healthy adults

Classification by specialty

Rehabilitation medicine Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To develop the effective muscle training

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Standing balance test, Center of pressure

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Cross-over

Randomization

Randomized

Randomization unit

Individual

Blinding

Single blind -participants are blinded

Control

Active

Stratification

YES

Dynamic allocation

NO

Institution consideration

Institution is not considered as adjustment factor.

Blocking

NO

Concealment

Central registration


Intervention

No. of arms

2

Purpose of intervention

Educational,Counseling,Training

Type of intervention

Maneuver

Interventions/Control_1

Muscle strength training(Block ex.)

Interventions/Control_2

Muscle strength training(Random order ex.)

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


Not applicable

Gender

Male and Female

Key inclusion criteria

Give a written informed consent to the participation in the present study

Key exclusion criteria

1.Suspected of severe dementia
2.Have a problem with the safe implementation of exercise

Target sample size

60


Research contact person

Name of lead principal investigator

1st name Satoshi
Middle name
Last name Kasahara

Organization

Hokkaido University

Division name

Department of Rehabilitation Science, Faculty of Health Sciences

Zip code

060-0812

Address

Kita 12 Nishi 5, Kita-Ku, Sapporo, Hokkaido, Japan

TEL

011-706-3390

Email

kasahara@hs.hokudai.ac.jp


Public contact

Name of contact person

1st name Satoshi
Middle name
Last name Kasahara

Organization

Hokkaido University

Division name

Department of Rehabilitation Science, Faculty of Health Sciences

Zip code

060-0812

Address

Kita 12 Nishi 5, Kita-Ku, Sapporo, Hokkaido, Japan

TEL

011-706-3390

Homepage URL


Email

kasahara@hs.hokudai.ac.jp


Sponsor or person

Institute

Hokkaido University

Institute

Department

Personal name



Funding Source

Organization

Hokkaido 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

Hokkaido University, Department of Rehabilitation Science, Faculty of Health Sciences

Address

Kita 12 Nishi 5, Kita-Ku, Sapporo, Hokkaido, Japan

Tel

011-706-3316

Email

shomu@hs.hokudai.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

2021 Year 10 Month 12 Day


Related information

URL releasing protocol

https://www.tandfonline.com/doi/full/10.1080/00222895.2025.2505496

Publication of results

Published


Result

URL related to results and publications

https://www.tandfonline.com/doi/full/10.1080/00222895.2025.2505496

Number of participants that the trial has enrolled

20

Results

Both constant and random practice improved bilateral strength capacity. Immediately after practice, standing balance improved in both groups. However, the improvement in standing balance was maintained only in the random practice group.

Results date posted

2025 Year 04 Month 28 Day

Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics

Healthy young adults

Participant flow

join the volunteer

Adverse events

No

Outcome measures

Muscle strength test, balance test

Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2021 Year 10 Month 01 Day

Date of IRB

2021 Year 11 Month 02 Day

Anticipated trial start date

2021 Year 11 Month 02 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

2021 Year 10 Month 12 Day

Last modified on

2026 Year 04 Month 09 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000052201