UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000039627
Receipt number R000045146
Scientific Title Evaluation of quality of inpatient rehabilitation based on patient experience - Development of Japanese version Client Centered Rehabilitation Questionnaire-.
Date of disclosure of the study information 2020/03/15
Last modified on 2024/03/02 09:02:27

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Basic information

Public title

Evaluation of quality of inpatient rehabilitation based on patient experience - Development of Japanese version Client Centered Rehabilitation Questionnaire-.

Acronym

Development of Japanese version Client Centered Rehabilitation Questionnaire.

Scientific Title

Evaluation of quality of inpatient rehabilitation based on patient experience - Development of Japanese version Client Centered Rehabilitation Questionnaire-.

Scientific Title:Acronym

Development of Japanese version Client Centered Rehabilitation Questionnaire

Region

Japan


Condition

Condition

Patients receiving inpatient rehabilitation

Classification by specialty

Rehabilitation medicine Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study is to develop a Japanese version Client Centered Rehabilitation Questionnaire that evaluates the value of patient experience in inpatient rehabilitation.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Construct validity
Convergent validity
Discriminant validity
Test-retest reliability

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

Patients with cognitive function that can answer questionnaires.
Patients who have been hospitalized for more than 30 days in Kaifukuki rehabilitation ward and are expected to be discharged within one week.
Patients over 18 years old.

Key exclusion criteria

Patients who have not received a rehabilitation program.
Patients who not consent this study.

Target sample size

200


Research contact person

Name of lead principal investigator

1st name Shunta
Middle name
Last name Umeki

Organization

Re-FREE.LLC

Division name

Department of Administration

Zip code

870-0130

Address

1-24-24, Yokohigashimachi, Oita, Oita, Japan

TEL

090-7989-7021

Email

shunta.umeki@gmail.com


Public contact

Name of contact person

1st name Shunta
Middle name
Last name Umeki

Organization

Re-FREE.LLC

Division name

Department of Administration

Zip code

870-0130

Address

1-24-24, Yokohigashimachi, Oita, Oita, Japan

TEL

090-7989-7021

Homepage URL


Email

shunta.umeki@gmail.com


Sponsor or person

Institute

Re-FREE.LLC

Institute

Department

Personal name



Funding Source

Organization

Re-FREE.LLC

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

Oita Oka Hosputal

Address

3-7-11, Nishitsurusaki, Oita, Oita, Japan

Tel

097-522-2202

Email

nakano0097@keiwakai.oita.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

大分リハビリテーション病院


Other administrative information

Date of disclosure of the study information

2020 Year 03 Month 15 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

Terminated

Date of protocol fixation

2019 Year 12 Month 22 Day

Date of IRB

2020 Year 01 Month 14 Day

Anticipated trial start date

2020 Year 04 Month 01 Day

Last follow-up date

2022 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

For patients admitted to the Oita Rehabilitation Hospital between April 2020 and March 2022.


Management information

Registered date

2020 Year 02 Month 28 Day

Last modified on

2024 Year 03 Month 02 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000045146


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name