UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000030672
Receipt number R000035019
Scientific Title Validity examination of using the measurement machine of wrist spasticity
Date of disclosure of the study information 2018/01/04
Last modified on 2019/07/26 07:41:18

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Basic information

Public title

Validity examination of using the measurement machine of wrist spasticity

Acronym

Validity examination of measurement of spasticity

Scientific Title

Validity examination of using the measurement machine of wrist spasticity

Scientific Title:Acronym

Validity examination of measurement of spasticity

Region

Japan


Condition

Condition

central nerve disorder

Classification by specialty

Rehabilitation medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To study the validity of the measurement machine of wrist spasticity

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

the correlation between the force of
wrist and clinical score of the spasticity

Key secondary outcomes

the correlation between the force of
wrist and range of motion


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

Diagnosis

Type of intervention

Device,equipment

Interventions/Control_1

measurement by the measurement machine of wrist spasticity

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

16 years-old <=

Age-upper limit

80 years-old >=

Gender

Male and Female

Key inclusion criteria

the patients of cetral nerve disorder
the patients who have paretic uper limbs (Modified Ashworth Scale 0-3)
inpatients and outpatients of Kagoshima University Hospital

Key exclusion criteria

the patients who have painful upper limbs.
the patients who are difficult to understand the examination.
the patients who are decided unsuitable for this examination by medical dotor.


Target sample size

20


Research contact person

Name of lead principal investigator

1st name Seiji
Middle name
Last name Etoh

Organization

Guraduate school of Kagoshima University

Division name

Department of physical medicine and rehabilitation

Zip code

8908520

Address

8-35-1, Sakuragaoka, Kagoshima city

TEL

0992755339

Email

etohs@m2.kufm.kagoshima-u.ac.jp


Public contact

Name of contact person

1st name Seiji
Middle name
Last name Etoh

Organization

Guraduate school of Kagoshima University

Division name

Department of physical medicine and rehabilitation

Zip code

8908520

Address

8-35-1, Sakuragaoka, Kagoshima city

TEL

0992755339

Homepage URL


Email

etohs@m2.kufm.kagoshima-u.ac.jp


Sponsor or person

Institute

Kagoshima University Hospital

Institute

Department

Personal name



Funding Source

Organization

Kagoshima University Hospital

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

Guraduate school of Kagoshima University

Address

8-35-1, Sakuragaoka, Kagoshima city

Tel

0992755339

Email

etohs@m2.kufm.kagoshima-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 01 Month 04 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

Enrolling by invitation

Date of protocol fixation

2017 Year 12 Month 01 Day

Date of IRB

2017 Year 11 Month 27 Day

Anticipated trial start date

2018 Year 01 Month 04 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



Other

Other related information



Management information

Registered date

2018 Year 01 Month 04 Day

Last modified on

2019 Year 07 Month 26 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000035019


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name