UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000053927
Receipt number R000061553
Scientific Title A survey for home-visiting nurse perceptions of transdermal patches for individuals with dementia
Date of disclosure of the study information 2024/03/25
Last modified on 2025/03/21 09:21:31

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Basic information

Public title

A survey for home-visiting nurse perceptions of transdermal patches for individuals with dementia

Acronym

A survey for home-visiting nurse perceptions of transdermal patches for individuals with dementia

Scientific Title

A survey for home-visiting nurse perceptions of transdermal patches for individuals with dementia

Scientific Title:Acronym

A survey for home-visiting nurse perceptions of transdermal patches

Region

Japan


Condition

Condition

Not applicable

Classification by specialty

Nursing

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The aim of this study is to investigate medication support provided by home-visiting nurses to individuals with dementia, focusing specifically on their understanding of medication forms, particularly transdermal patches.

Basic objectives2

Others

Basic objectives -Others

Awareness survey of transdermal patches

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Awareness of home-visiting nurse regarding the use of transdermal patches for Alzheimer's disease patients

Key secondary outcomes



Base

Study type

Others,meta-analysis etc


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


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

18 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

(1)18 years or older at the time of obtaining consent
(2)home-visiting nurse who meet all of the following criteria
-Works at a home-visit nursing station (administrator, staff), or works at a hospital or clinic
-Responsible for one or more users received long-term care certification

Key exclusion criteria

If multiple answers are given, only the final answer will be used for analysis.

Target sample size

400


Research contact person

Name of lead principal investigator

1st name Atsushi
Middle name
Last name Kasano

Organization

Kowa Company. Ltd.

Division name

Medical Affairs Management Department

Zip code

1030023

Address

4-10, Nihonbashi-honcho 3-chome, Chuo-ku, Tokyo

TEL

0332797917

Email

a-kasano@kowa.co.jp


Public contact

Name of contact person

1st name Kazuyuki
Middle name
Last name Tsujimoto

Organization

Kowa Company. Ltd.

Division name

Medical Affairs Department 1

Zip code

1030023

Address

4-10, Nihonbashi-honcho 3-chome, Chuo-ku, Tokyo

TEL

0332797424

Homepage URL


Email

k-tsujimoto@kowa.co.jp


Sponsor or person

Institute

Kowa Company. Ltd.

Institute

Department

Personal name



Funding Source

Organization

Kowa Company. Ltd.

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Kowa Company. Ltd.

Address

4-10, Nihonbashi-honcho 3-chome, Chuo-ku, Tokyo 103-0023 JAPAN

Tel

0332797424

Email

k-tsujimoto@kowa.co.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

2024 Year 03 Month 25 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

2024 Year 03 Month 19 Day

Date of IRB

2024 Year 03 Month 19 Day

Anticipated trial start date

2024 Year 03 Month 27 Day

Last follow-up date

2024 Year 06 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

N/A


Management information

Registered date

2024 Year 03 Month 21 Day

Last modified on

2025 Year 03 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000061553