UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000049924
Receipt number R000056862
Scientific Title Examination of usefulness of remote support application for cochlear implant
Date of disclosure of the study information 2022/12/28
Last modified on 2022/12/27 20:31:54

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Examination of usefulness of remote support application for cochlear implant users

Acronym

Usefulness of remote support application for cochlear implant users

Scientific Title

Examination of usefulness of remote support application for cochlear implant

Scientific Title:Acronym

Usefulness of remote support app for cochlear implants

Region

Japan


Condition

Condition

After cochlear implant surgery

Classification by specialty

Oto-rhino-laryngology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Cochlear implants require periodical confirmation and adjustment of hearing conditions after surgery. Therefore, regular visits to the hospital are necessary, but the visits to the hospital are a heavy burden for the wearer who lives far away or who finds it difficult to see a doctor due to reasons such as school or work. Therefore, we aim to evaluate whether the remote support application contributes to reducing the burden on patients.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Usage experience of the remote support application (remote check), necessity of training, degree of satisfaction, points of dissatisfaction, changes in the frequency and necessity of visiting medical institutions, listening conditions/sound quality, mapping parameters, device parameters such as impedance

Key secondary outcomes

Utilization of information provided as feedback to wearers and guardians


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

Educational,Counseling,Training

Type of intervention

Other

Interventions/Control_1

We will provide participants in this study with a remote support application (remote check) that allows them to check the hearing status of their cochlear implants, and have them use the remote check for more than half a year.

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

4 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Cochlear implant recipients who underwent cochlear implant surgery at our hospital and are using Cochlear N7 or Kanso2

Key exclusion criteria

Patients who do not agree to participate in research, patients who cannot visit the hospital regularly

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Kenichi
Middle name
Last name Takano

Organization

Sapporo Medical University

Division name

Otolaryngology, Head and Neck Surgery

Zip code

060-8556

Address

South-1, West-16, Chuo-ku, Sapporo, Hokkaido, Japan

TEL

011-611-2111

Email

kent@sapmed.ac.jp


Public contact

Name of contact person

1st name Takuya
Middle name
Last name Kakuki

Organization

Sapporo Medical University

Division name

Otolaryngology, Head and Neck Surgery

Zip code

060-8556

Address

South-1, West-16, Chuo-ku, Sapporo, Hokkaido, Japan

TEL

011-611-2111

Homepage URL


Email

t.kakuki@sapmed.ac.jp


Sponsor or person

Institute

Sapporo Medical University

Institute

Department

Personal name



Funding Source

Organization

Ministry of education

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

Sapporo Medical University, Hospital Clinical Research Review Committee

Address

South-1, West-16, Chuo-ku, Sapporo, Hokkaido, Japan

Tel

011-611-2111

Email

ji-rskk@sapmed.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

2022 Year 12 Month 28 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

Open public recruiting

Date of protocol fixation

2022 Year 05 Month 12 Day

Date of IRB

2022 Year 07 Month 14 Day

Anticipated trial start date

2022 Year 12 Month 27 Day

Last follow-up date

2024 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

2022 Year 12 Month 27 Day

Last modified on

2022 Year 12 Month 27 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000056862


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name