UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000032300
Receipt number R000036830
Scientific Title The effects of transcranial direct current stimulation combined with functional electrical stimulation on gait performance in stroke patients
Date of disclosure of the study information 2018/04/18
Last modified on 2019/10/20 10:30:01

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Basic information

Public title

The effects of transcranial direct current stimulation combined with functional electrical stimulation on gait performance in stroke patients

Acronym

The effects of tDCS combined with FES in stroke patients

Scientific Title

The effects of transcranial direct current stimulation combined with functional electrical stimulation on gait performance in stroke patients

Scientific Title:Acronym

The effects of tDCS combined with FES in stroke patients

Region

Japan


Condition

Condition

stroke

Classification by specialty

Rehabilitation medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To investigate whether or not transcranial direct current stimulation combined with functional electrical stimulation would improve gait performance of patients with post-stroke

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

10-meter walking test
walking during body sway

Key secondary outcomes

fugl-meyer assessment (the lower extremity)
stroke impairment assessment set (foot-pat test)
modified ashworth scale


Base

Study type

Interventional


Study design

Basic design

Cross-over

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -but assessor(s) are blinded

Control

Placebo

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

transcranial direct current stimulation combined with functional electrical stimulation

Interventions/Control_2

sham stimulation combined with functional electrical stimulation

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

1) Consent to participate in the study
2) The ability to walk without support for at least 16-meters
3) The score of SIAS foot-pat test is 1 or more.
4) Capability of communicating and understanding instructions

Key exclusion criteria

1) Contraindications for electrical stimulation
2) Severe sensory deficits
3) Neurological condition unrelated to stroke hemiparesis

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Tsubasa
Middle name
Last name Mitsutake

Organization

Shiroishi Kyoritsu Hospital

Division name

Department of Rehabilitation

Zip code

849-1112

Address

1296 Fukuta, Shiroishi-cho, Kishima-gun, Saga

TEL

0952-84-6060

Email

mitutuba1012@gmail.com


Public contact

Name of contact person

1st name Tsubasa
Middle name
Last name Mitsutake

Organization

Shiroishi Kyoritsu Hospital

Division name

Department of Rehabilitation

Zip code

849-1112

Address

1296 Fukuta, Shiroishi-cho, Kishima-gun, Saga

TEL

0952-84-6060

Homepage URL


Email

mitutuba1012@gmail.com


Sponsor or person

Institute

Shiroishi Kyoritsu Hospital

Institute

Department

Personal name



Funding Source

Organization

nothing

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

Shiroishi Kyoritsu Hospital

Address

1296 Fukuta, Shiroishi-cho, Kishima-gun, Saga

Tel

0952-84-6060

Email

mitutuba1012@gmail.com


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 04 Month 18 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

Completed

Date of protocol fixation

2018 Year 04 Month 18 Day

Date of IRB

2018 Year 04 Month 03 Day

Anticipated trial start date

2018 Year 04 Month 18 Day

Last follow-up date

2019 Year 10 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 04 Month 18 Day

Last modified on

2019 Year 10 Month 20 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000036830


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name