UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000063068
Receipt number R000072197
Scientific Title A Study on How Video Records Support Understanding of Falls and Planning Safety Measures
Date of disclosure of the study information 2026/09/28
Last modified on 2026/09/28 10:25:36

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Basic information

Public title

A Study on How Video Records Support Understanding of Falls and Planning Safety Measures

Acronym

A Study on How Video Records Support Understanding of Falls and Planning Safety Measures

Scientific Title

A Study on How Video Records Support Understanding of Falls and Planning Safety Measures

Scientific Title:Acronym

A Study on How Video Records Support Understanding of Falls and Planning Safety Measures

Region

Japan


Condition

Condition

Patients admitted to a Comprehensive Rehabilitation Ward
Staff working in the Comprehensive Rehabilitation Ward

Classification by specialty

Rehabilitation medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To examine how image records affect fall situation understanding and safety measure planning among rehabilitation ward staff and inpatients.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Agreement between pre - and post - image assessments of fall circumstances and proposed safety measures

Key secondary outcomes

Confidence levels (certainty) in pre - and post - video assessments of fall circumstances and proposed safety measures


Base

Study type

Observational


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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients
1. Individuals who provide written informed consent based on sufficient explanation and adequate understanding of the study.
2. Individuals for whom image recording using a camera-type sensor is conducted as part of routine clinical care.
3. Individuals who experienced a fall in their room.
4. Individuals who are able to respond to questions regarding "fall circumstances" and "proposed safety measures".

Staff
1. Individuals who provide written informed consent based on sufficient explanation and adequate understanding of the study.
2. Individuals who routinely participate in post-fall reviews as part of standard clinical practice.

Key exclusion criteria

Individuals judged as inappropriate for participation by the principal investigator or co - investigators.

Target sample size

70


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, Japan

TEL

0562-93-2167

Email

cent-rsh@fujita-hu.ac.jp


Public contact

Name of contact person

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, Japan

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, Japan

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

2026 Year 09 Month 28 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

2026 Year 09 Month 28 Day

Date of IRB

2026 Year 09 Month 07 Day

Anticipated trial start date

2026 Year 09 Month 28 Day

Last follow-up date

2029 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

None


Management information

Registered date

2026 Year 09 Month 28 Day

Last modified on

2026 Year 09 Month 28 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000072197