UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000044056
Receipt number R000049740
Scientific Title Effect of high and low frequency neuromuscular electrical stimulation therapy for swallowing function
Date of disclosure of the study information 2021/06/30
Last modified on 2021/04/27 19:27:12

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Basic information

Public title

Effect of high and low frequency neuromuscular electrical stimulation therapy for swallowing function

Acronym

Effect of high and low frequency neuromuscular electrical stimulation therapy for swallowing function

Scientific Title

Effect of high and low frequency neuromuscular electrical stimulation therapy for swallowing function

Scientific Title:Acronym

Effect of high and low frequency neuromuscular electrical stimulation therapy for swallowing function

Region

Japan


Condition

Condition

healthy elderly

Classification by specialty

Rehabilitation medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to clarifie the effective intervention frequency of neuromuscular electrical stimulation therapy.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Videofluorography

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Dose comparison

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Device,equipment Maneuver

Interventions/Control_1

Three times interventions a week(4 weeks)

Interventions/Control_2

Weekly intervention(4 weeks)

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

70 years-old <=

Age-upper limit

90 years-old >=

Gender

Male and Female

Key inclusion criteria

Elderly people without dysphagia

Key exclusion criteria

artificial cardiac pacemaker user,dysphagia,cognitive function decline,tracheolytic openings,digestive tract,acute bleeding,blockage

Target sample size

50


Research contact person

Name of lead principal investigator

1st name maya
Middle name
Last name nakahira

Organization

Kochi Medical School Hospital

Division name

Department of Rehabilitation Center

Zip code

7838505

Address

Kohasu, Okou, Nankoku, Kochi, Japan.

TEL

0888802490

Email

jm-nakahira-m@kochi-u.ac.jp


Public contact

Name of contact person

1st name maya
Middle name
Last name nakahira

Organization

Kochi Medical School Hospital

Division name

Department of Rehabilitation Center

Zip code

7838505

Address

Kohasu, Okou, Nankoku, Kochi, Japan.

TEL

0888802490

Homepage URL


Email

jm-nakahira-m@kochi-u.ac.jp


Sponsor or person

Institute

Kochi Medical School Hospital

Institute

Department

Personal name



Funding Source

Organization

Japan Society for the Promotion of Science

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

Kochi Medical School

Address

Kohasu, Okou, Nankoku, Kochi, Japan.

Tel

088-880-2180

Email

is21@kochi-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

2021 Year 06 Month 30 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

2021 Year 06 Month 30 Day

Date of IRB


Anticipated trial start date

2021 Year 06 Month 30 Day

Last follow-up date

2025 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

2021 Year 04 Month 27 Day

Last modified on

2021 Year 04 Month 27 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000049740


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name