UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000056453
Receipt number R000064511
Scientific Title Development of an assessment measure for mobility in bed.
Date of disclosure of the study information 2024/12/13
Last modified on 2024/12/13 17:23:59

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Basic information

Public title

Development of an assessment measure for mobility in bed.

Acronym

Development of an assessment measure for mobility in bed.

Scientific Title

Development of an assessment measure for mobility in bed.

Scientific Title:Acronym

Development of an assessment measure for mobility in bed.

Region

Japan


Condition

Condition

Healthy subjects
Rehabilitation subjects

Classification by specialty

Rehabilitation medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To study the reliability and validity of a sensitive assessment tool for activities of daily living on a bed.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

How to perform basic movements such as rolling and getting up in bed, and the time required for them.

Key secondary outcomes

Basic information such as age, gender, and body mass index.
Rivermead Mobility Index and Functional Independence Measure.
Kinematic parameters using three-dimensional motion analysis devices and inertial sensors, and surface electromyography measurements.
Assessment using pressure sensors, etc.
Subjective comfort questionnaire.


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Prevention

Type of intervention

Other

Interventions/Control_1

Activities of daily living such as rolling, getting up, a sitting position, and standing up are carried out on various mattresses.

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


Not applicable

Gender

Male and Female

Key inclusion criteria

1)Healthy subjects
People who have no history of stroke, neurological or muscular disease, bone or joint disease, heart disease, or mental illness, and who can provide informed consent for this study.

2)Rehabilitation subjects
Inpatients with disabilities who have given informed consent for this study.

Key exclusion criteria

1)Healthy subjects
People with a history of stroke, neurological or muscular disease, bone or joint disease, heart disease, or psychiatric disease.

2)Rehabilitation subjects
Patients whose general condition is unstable and who may experience sudden changes.
Patients who have difficulty following instructions when performing tasks due to cognitive impairment.

Target sample size

400


Research contact person

Name of lead principal investigator

1st name Yohei
Middle name
Last name Otaka

Organization

Fujita Health University

Division name

Department of Rehabilitation Medicine,school of Medicine

Zip code

470-1192

Address

1-98, Dengakugakubo, Kutsukake-cho, Toyoake, Aichi

TEL

0562-93-2167

Email

yootaka@fujita-hu.ac.jp


Public contact

Name of contact person

1st name Hirofumi
Middle name
Last name Ota

Organization

Fujita Health University

Division name

Faculty of Rehabilitation, School of Health Sciences

Zip code

470-1192

Address

1-98, Dengakugakubo, Kutsukake-cho, Toyoake, Aichi

TEL

0562-93-9000

Homepage URL


Email

hiro0527@fujita-hu.ac.jp


Sponsor or person

Institute

Fujita Health University

Institute

Department

Personal name



Funding Source

Organization

Fujita Health University

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Ethics Review Committee of Fujita Health University

Address

1-98 Dengakugakubo, Kutukake-cho, Toyoake, Aichi

Tel

0562-93-2865

Email

f-irb@fujita-hu.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 12 Month 13 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

Enrolling by invitation

Date of protocol fixation

2020 Year 04 Month 10 Day

Date of IRB

2020 Year 04 Month 10 Day

Anticipated trial start date

2020 Year 04 Month 10 Day

Last follow-up date

2027 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

2024 Year 12 Month 13 Day

Last modified on

2024 Year 12 Month 13 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000064511