UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000058924
Receipt number R000067390
Scientific Title Effects of dysesthesia-matched transcutaneous electrical nerve stimulation on impaired grasp control due to dysesthesias after spinal cord injury.
Date of disclosure of the study information 2025/08/29
Last modified on 2025/08/29 11:17:39

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Basic information

Public title

Effects of dysesthesia-matched transcutaneous electrical nerve stimulation on impaired grasp control due to dysesthesias after spinal cord injury.

Acronym

Effects of dysesthesia-matched transcutaneous electrical nerve stimulation on impaired grasp control due to dysesthesias after spinal cord injury.

Scientific Title

Effects of dysesthesia-matched transcutaneous electrical nerve stimulation on impaired grasp control due to dysesthesias after spinal cord injury.

Scientific Title:Acronym

Effects of dysesthesia-matched transcutaneous electrical nerve stimulation on impaired grasp control due to dysesthesias after spinal cord injury.

Region

Japan


Condition

Condition

spinal cord injury

Classification by specialty

Rehabilitation medicine Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the effects of dysesthesia-matched transcutaneous electrical nerve stimulation on grasp control impairment in individuals with spinal cord injury.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

grip force

Key secondary outcomes

load force


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

3

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

dysesthesia-matched transcutaneous electrical nerve stimulation

Interventions/Control_2

no dysesthesia-matched transcutaneous electrical nerve stimulation

Interventions/Control_3

control

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

18 years-old <=

Age-upper limit

90 years-old >=

Gender

Male and Female

Key inclusion criteria

Individual with spinal cord injury: diagnosis of spinal cord injury, Healthy adult: No apparent physical disability, No diagnosis of dementia

Key exclusion criteria

Patients with difficulty in understanding and performing tasks, patients with higher brain dysfunction, patients with recurrent or concurrent central or peripheral neurological disorders, patients with upper limb musculoskeletal disorders, and patients with implanted electrodes such as pacemakers.

Target sample size

26


Research contact person

Name of lead principal investigator

1st name Nishi
Middle name
Last name Yuki

Organization

Nagasaki university

Division name

Biomedical Sciences (Health Sciences)

Zip code

852-8520

Address

1-7-1,sakamoto,nagasaki

TEL

095-819-7967

Email

ynishi@nagasaki-u.ac.jp


Public contact

Name of contact person

1st name Yuki
Middle name
Last name Nishi

Organization

Nagasaki university

Division name

Biomedical Sciences (Health Sciences)

Zip code

852-8520

Address

1-7-1,sakamoto,nagasaki

TEL

095-819-7967

Homepage URL


Email

ynishi@nagasaki-u.ac.jp


Sponsor or person

Institute

Nagasaki university

Institute

Department

Personal name



Funding Source

Organization

self

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Nishiyamato Rehabilitation Hospital

Address

3-2-2, kitakatsuragi-gun, nara

Tel

0745716688

Email

index2424@gmail.com


Secondary IDs

Secondary IDs

YES

Study ID_1

060

Org. issuing International ID_1

Nishiyamato Rehabilitation Hospital

Study ID_2


Org. issuing International ID_2


IND to MHLW

奈良県


Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2025 Year 08 Month 29 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

2024 Year 08 Month 20 Day

Date of IRB

2024 Year 10 Month 10 Day

Anticipated trial start date

2025 Year 08 Month 29 Day

Last follow-up date

2026 Year 08 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2025 Year 08 Month 29 Day

Last modified on

2025 Year 08 Month 29 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067390