UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000029938
Receipt number R000034199
Scientific Title Clinical study on effect of home exercise in patients with spinocerebellar degeneration
Date of disclosure of the study information 2017/11/15
Last modified on 2020/09/28 19:23:09

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Basic information

Public title

Clinical study on effect of home exercise in patients with spinocerebellar degeneration

Acronym

Effect of home exercise in patients with spinocerebellar degeneration

Scientific Title

Clinical study on effect of home exercise in patients with spinocerebellar degeneration

Scientific Title:Acronym

Effect of home exercise in patients with spinocerebellar degeneration

Region

Japan


Condition

Condition

Spinocerebellar Degeneration

Classification by specialty

Rehabilitation medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Spinocerebellar degeneration (SCD) is a generic term for neurological disorders whose main symptom is cerebellar ataxia.
Daily living behavior (ADL) is markedly impaired as symptoms progress.
Regarding the effect of rehabilitation (rehabilitation), it has been reported that improvements in cerebellar ataxia ataxia evaluation and walking have been observed by short-term intensive rehabilitation and home exercise (Home ex.).
However, these reports have verified effects of comparatively long interventions focusing on overall ataxia and gait, and effects on upper limb function and ADL has yet to be clarified.
Therefore, the purpose of this study is to verify effects of Home ex. for a short time specialized in "upper limb function and ADL" for SCD patients.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Scale for the assessment and rating of ataxia.
Evaluate before intervention (start of intervention, 4 weeks) and after intervention (8 weeks).

Key secondary outcomes

9-Hole Peg Test
Functional Independence Measure
Beck Depression Inventory-Second Edition
SF8 Health Survey
Evaluate before intervention (start of intervention, 4 weeks) and after intervention (8 weeks).


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

Treatment

Type of intervention

Behavior,custom

Interventions/Control_1

The content of exercise intervention is 4 weeks Home ex.
The contents of that will be repeatedly conducted ADL action guidance that the subject is struggling with at home.
Home ex. Is carried out for 20 minutes / times*5 days a week*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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Cases present spinocerebellar degeneration and can be done Home.ex.

Key exclusion criteria

Cases show a decline in prominent cognitive function and can not be done Home.ex.

Target sample size

16


Research contact person

Name of lead principal investigator

1st name Takehito
Middle name
Last name YONEZAWA

Organization

Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan

Division name

Department of Community-based Rehabilitation Sciences

Zip code

852-8511

Address

1-7-1, Sakamoto, Nagasaki, Japan

TEL

095-819-7904

Email

mikemizuno@hotmail.com


Public contact

Name of contact person

1st name Takehito
Middle name
Last name YONEZAWA

Organization

Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan

Division name

Department of Community-based Rehabilitation Sciences

Zip code

852-8511

Address

1-7-1, Sakamoto, Nagasaki, Japan

TEL

095-819-7904

Homepage URL


Email

mikemizuno@hotmail.com


Sponsor or person

Institute

Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan

Institute

Department

Personal name



Funding Source

Organization

Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan

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

Nagasaki University Graduate School of Biomedical Sciences

Address

1-12-4 sakamoto-mati, nagasaki-si, nagasaki-ken

Tel

095-819-7195

Email

gakujutu_kikaku@ml.nagasaki-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

長崎大学病院


Other administrative information

Date of disclosure of the study information

2017 Year 11 Month 15 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

No longer recruiting

Date of protocol fixation

2018 Year 03 Month 25 Day

Date of IRB

2018 Year 04 Month 16 Day

Anticipated trial start date

2018 Year 04 Month 16 Day

Last follow-up date

2019 Year 03 Month 31 Day

Date of closure to data entry

2019 Year 03 Month 31 Day

Date trial data considered complete

2019 Year 09 Month 07 Day

Date analysis concluded



Other

Other related information



Management information

Registered date

2017 Year 11 Month 12 Day

Last modified on

2020 Year 09 Month 28 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000034199


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name