UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000033166
Receipt number R000037606
Scientific Title Measurement of shock absorption ability and knee joint sway in frontal plane during landing task using the accelerometer
Date of disclosure of the study information 2018/07/01
Last modified on 2019/06/29 11:44:57

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Measurement of shock absorption ability and knee joint sway in frontal plane during landing task using the accelerometer

Acronym

Measurement of shock absorption ability and knee joint sway in frontal plane during landing task using the accelerometer

Scientific Title

Measurement of shock absorption ability and knee joint sway in frontal plane during landing task using the accelerometer

Scientific Title:Acronym

Measurement of shock absorption ability and knee joint sway in frontal plane during landing task using the accelerometer

Region

Japan


Condition

Condition

Healthy adult male or female

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To clarify the reliability and validity of shock absorption ability and knee joint sway in frontal plane during landing task, and the relationship between knee joint sway in frontal plane and lower extremity motion during landing task.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The shock absorption ability using the accelerometer or the force plate

Key secondary outcomes

The knee joint sway in frontal plane using the accelerometer


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Prevention

Type of intervention

Other

Interventions/Control_1

Three trial on single-leg landing from 30 cm height

Interventions/Control_2


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

19 years-old <

Age-upper limit

30 years-old >

Gender

Male and Female

Key inclusion criteria

healthy adult male or female in their twenties
Belong to the basketball club or the volleyball club in the university

Key exclusion criteria

Persons who had a history of orthopedic or neurological diseases
Those who did not obtain consent

Target sample size

30


Research contact person

Name of lead principal investigator

1st name Masaaki
Middle name
Last name Sakamoto

Organization

Gunma University

Division name

Graduate School of Healthy Sciences

Zip code

371-8514

Address

3-39-22 Showa, Maebashi, Gunma

TEL

027-220-8972

Email

msaka@gunma-u.ac.jp


Public contact

Name of contact person

1st name Shogo
Middle name
Last name Okamoto

Organization

Gunma University

Division name

Graduate School of Healthy Sciences

Zip code

371-8514

Address

3-58-7-102 Kamikoide, Maebashi, Gunma

TEL

090-4679-5762

Homepage URL


Email

m14711027@gunma-u.ac.jp


Sponsor or person

Institute

Gunma University

Institute

Department

Personal name



Funding Source

Organization

None

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Department of clinical examination, Gunma University Hospital

Address

3-39-15 Showa, Maebashi, Gunma

Tel

027-220-8740

Email

hitotaisho-ciru@ml.gunma-u.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

2018 Year 07 Month 01 Day


Related information

URL releasing protocol


Publication of results

Published


Result

URL related to results and publications


Number of participants that the trial has enrolled

10

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

2018 Year 07 Month 01 Day

Date of IRB

2018 Year 07 Month 20 Day

Anticipated trial start date

2018 Year 07 Month 25 Day

Last follow-up date

2019 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded

2018 Year 11 Month 01 Day


Other

Other related information



Management information

Registered date

2018 Year 06 Month 27 Day

Last modified on

2019 Year 06 Month 29 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000037606


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name