UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000020515
Receipt number R000023685
Scientific Title Anti-spastic effect of wrist extension orthosis in post-stroke patients: A pilot study
Date of disclosure of the study information 2016/01/10
Last modified on 2016/01/30 23:09:22

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Basic information

Public title

Anti-spastic effect of wrist extension orthosis in post-stroke patients: A pilot study

Acronym

Anti-spastic effect of wrist extension orthosis in post-stroke patients

Scientific Title

Anti-spastic effect of wrist extension orthosis in post-stroke patients: A pilot study

Scientific Title:Acronym

Anti-spastic effect of wrist extension orthosis in post-stroke patients

Region

Japan


Condition

Condition

Post-stroke patients

Classification by specialty

Neurology Rehabilitation medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To investigate the effect of wrist extension orthosis

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

modified Tardieu scale and modified Ashworth scale (MAS) at baseline and after 4-week intervention

Key secondary outcomes

Fugl-Meyer assessment (FMA), Brunnstrom recovery stage, passive range of motion (P-ROM), active range of motion (A-ROM), visual analogue scale VAS), functional independence measure (FIM)


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Self control

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

Intervention with the wrist extension orthosis is scheduled 6 hours/day, six times a week, for 4 weeks.

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

20 years-old <=

Age-upper limit

90 years-old >

Gender

Male and Female

Key inclusion criteria

post-stroke patients with hemiplegia; more than 1 month after the onset of stroke and stable condition; Brunnstrom recovery stage of upper limb >III; pastic wrist and finger; imformed consent

Key exclusion criteria

severe higher brain dysfuncction and dementia, conscious disturbance; joint disformation of upper limb; severe sensory disturbance; severe skin disease

Target sample size

30


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Shuji Matsumoto

Organization

Kagoshima University

Division name

Dept. of Rehabilitation

Zip code


Address

3930-7 Takachiho, Makizono-cho, Kirishima City

TEL

0995-78-2538

Email

shushu@m.kufm.kagoshima-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Shuji Matsumoto

Organization

Kagoshima University

Division name

Dept. of Rehabilitation

Zip code


Address

3930-7 Takachiho, Makizono-cho, Kirishima City

TEL

0995-78-2538

Homepage URL


Email

shushu@m.kufm.kagoshima-u.ac.jp


Sponsor or person

Institute

Kagoshima University

Institute

Department

Personal name



Funding Source

Organization

Kagoshima University

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


Address


Tel


Email



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

2016 Year 01 Month 10 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

2016 Year 01 Month 10 Day

Date of IRB


Anticipated trial start date

2016 Year 01 Month 15 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2016 Year 01 Month 10 Day

Last modified on

2016 Year 01 Month 30 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000023685


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name