UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000055973
Receipt number R000063846
Scientific Title Standardizing discharge processes by providing pre-written instructions for home care support to emergency department patients
Date of disclosure of the study information 2024/10/30
Last modified on 2025/04/30 09:01:53

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Basic information

Public title

Standardizing discharge processes by providing pre-written instructions for home care support to emergency department patients

Acronym

Standardizing discharge processes by providing pre-written instructions for home care support to emergency department patients

Scientific Title

Standardizing discharge processes by providing pre-written instructions for home care support to emergency department patients

Scientific Title:Acronym

Standardizing discharge processes by providing pre-written instructions for home care support to emergency department patients

Region

Japan


Condition

Condition

N/A

Classification by specialty

Nursing

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to establish benefits of using "Symptom-Specific Home Care Manual" by conducting a survey of nurses used the manual. Compare the outcomes before and after use of the manual, and propose for all the ED nurses to implement home care support in the same manner, regardless of seniority and work experience.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Compare changes before and after using the "Symptom-Specific Home Care Manual."

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Historical

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Educational,Counseling,Training

Type of intervention

Behavior,custom

Interventions/Control_1

For approximately three months, the "Symptom-Specific Home Support Manual" will be used to provide home support to patients who visited the emergency department with "fever symptoms," "cuts, contusions, lacerations, bruises," and "abdominal pain and diarrhea."

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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

"Current status of post-discharge support at the emergency outpatient department of a core hospital in an area with a high elderly population rate."
*Data before the intervention will be taken from a previous study, "Current status of home-return support at the emergency outpatient department of a core hospital in an area with a high aging rate."

Key exclusion criteria

Nurses who were not in charge of the emergency outpatient department before using the "Symptom-Specific Home Support Manual."

Target sample size

90


Research contact person

Name of lead principal investigator

1st name Yui
Middle name
Last name Matsuoka

Organization

Dokkyo Medical University Nikko Medical Center

Division name

Nursing Department Emergency Department

Zip code

3211298

Address

145-1 Moritomo, Nikko City, Tochigi Prefecture

TEL

0288237000

Email

yui316@dokkyomed.ac.jp


Public contact

Name of contact person

1st name Yui
Middle name
Last name Matsuoka

Organization

Dokkyo Medical University Nikko Medical Center

Division name

Nursing Department Emergency Department

Zip code

3211298

Address

145-1 Moritomo, Nikko City, Tochigi Prefecture

TEL

0288237000

Homepage URL


Email

yui316@dokkyomed.ac.jp


Sponsor or person

Institute

Dokkyo Medical University Nikko Medical Center

Institute

Department

Personal name



Funding Source

Organization

N/A

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Dokkyo Medical University Nikko Medical Center Bioethics Committee

Address

145-1 Moritomo, Nikko City, Tochigi Prefecture

Tel

0288237000

Email

rinshokenkyu@dokkyomed.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

2024 Year 10 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

No longer recruiting

Date of protocol fixation

2024 Year 09 Month 06 Day

Date of IRB

2024 Year 09 Month 20 Day

Anticipated trial start date

2024 Year 10 Month 01 Day

Last follow-up date

2024 Year 12 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

2024 Year 10 Month 29 Day

Last modified on

2025 Year 04 Month 30 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000063846