UMIN-CTR Clinical Trial

Recruitment status Recruiting
Unique ID issued by UMIN UMIN000023477
Receipt No. R000027048
Official scientific title of the study The effect of neuromuscular electrical stimulation fo dysphagia: A before-and after study
Date of disclosure of the study information 2016/08/04
Last modified on 2016/08/04 (Ver. 1)

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Basic information
Official scientific title of the study The effect of neuromuscular electrical stimulation fo dysphagia: A before-and after study
Title of the study (Brief title) The NMES for dysphagia
Region
Japan

Condition
Condition Patients with brain injury
Classification by specialty
Rehabilitation medicine
Classification by malignancy Others
Genomic information NO

Objectives
Narrative objectives1 To investigate the effects of neuromuscular electrical stimulation (NMES) for patients with brain injury
Basic objectives2 Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes Video analysis
Key secondary outcomes fNIRS, questionnaire, blood pressure, heart rate, SpO2, adverse event

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
Maneuver
Interventions/Control_1 Neuromuscular electrical stimulation
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 1) duration after the onset of stroke > 1 month
2) patients with swalloing disorder
3) age is over 20 years
4) patients who agree to participate in this study

Key exclusion criteria 1) history of neurological disease
2) severe arrhythmia or pacemaker implantation
3) severe higher cortical dysfunction, dementia, loss of consciousness
4) severe sensory dysturabence or skin disease
Target sample size 20

Research contact person
Name of lead principal investigator Shuji Matsumoto
Organization Kagoshima University
Division name Dept. of Rehabilitation
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 Shuji Matsumoto
Organization Kagoshima University
Division name Dept. of Rehabilitation
Address 3930-7 Takachiho, Makizono-cho, Kirishima City
TEL 0995-78-2538
Homepage URL
Email shushu@m.kufm.kagoshima-u.ac.jp

Sponsor
Institute Kagoshima University
Institute
Department

Funding Source
Organization N/A
Organization
Division
Category of Funding Organization Self funding
Nationality of Funding Organization

Other related organizations
Co-sponsor
Name of secondary funder(s)

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 08 Month 04 Day

Progress
Recruitment status Recruiting
Date of protocol fixation
2016 Year 06 Month 14 Day
Anticipated trial start date
2016 Year 08 Month 04 Day
Last follow-up date
Date of closure to data entry
Date trial data considered complete
Date analysis concluded

Related information
URL releasing protocol
Publication of results Unpublished
URL releasing results
Results
Other related information

Management information
Registered date
2016 Year 08 Month 04 Day
Last modified on
2016 Year 08 Month 04 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000027048