UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000058299
Receipt number R000066646
Scientific Title Effect of wheelchair trolley structure on Caregivers' physical load during mobility assistance
Date of disclosure of the study information 2025/07/01
Last modified on 2025/06/27 10:23:21

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Basic information

Public title

Effect of wheelchair trolley structure on caregivers' physical load during mobility assistance

Acronym

The effect of wheelchair structures on physical load

Scientific Title

Effect of wheelchair trolley structure on Caregivers' physical load during mobility assistance

Scientific Title:Acronym

The effect of wheelchair structures on physical load

Region

Japan


Condition

Condition

Healthy adult

Classification by specialty

Rehabilitation medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To clarify the effects of two types of trolley structures, an omnidirectional trolley and a straight-ahead trolley, on the physical loads of caregivers and passengers during wheelchair mobility assistance.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Three-dimensional motion analysis
Electromyography

Key secondary outcomes

Time of task complete
Physical functions


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Other

Interventions/Control_1

Wheelchair of omnidirectional trolley

Interventions/Control_2

Wheelchair of straight-ahead trolley

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

65 years-old >

Gender

Male and Female

Key inclusion criteria

Consent to participate in this study
Participant whose general condition is stable

Key exclusion criteria

Participants who have difficulty understanding instructions
Participants who are judged to be inappropriate by the researcher

Target sample size

60


Research contact person

Name of lead principal investigator

1st name Yohei
Middle name
Last name Otak

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

0562-93-2168

Email

cent-rsh@fujita-hu.ac.jp


Public contact

Name of contact person

1st name Hikaru
Middle name
Last name Kondo

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

0562-93-9720

Homepage URL


Email

cent-rsh@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

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Institutional Review Board of Fujita Health University

Address

1-98 Dengakugakubo, Kutsukake-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

2025 Year 07 Month 01 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

2025 Year 05 Month 27 Day

Date of IRB

2025 Year 05 Month 27 Day

Anticipated trial start date

2025 Year 06 Month 01 Day

Last follow-up date

2029 Year 05 Month 27 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2025 Year 06 Month 27 Day

Last modified on

2025 Year 06 Month 27 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000066646