UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000043625
Receipt number R000049736
Scientific Title Correlation between ADL quantification using PLLA film and Barthel Index Score in elderly people.
Date of disclosure of the study information 2021/05/01
Last modified on 2023/09/27 12:49:24

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

ADL quantification using ankle device and Barthel Index Score in elderly people.

Acronym

ADL Study

Scientific Title

Correlation between ADL quantification using PLLA film and Barthel Index Score in elderly people.

Scientific Title:Acronym

PLLA-BI Study

Region

Japan


Condition

Condition

elderly

Classification by specialty

Geriatrics

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Quantification of activities of daily living by device

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

the integral Piezoelectric Poly L-lactic Acid Film amplitude

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

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Prevention

Type of intervention

Device,equipment

Interventions/Control_1

Subjects wear an ankle band with a built-in Piezoelectric Poly L-lactic Acid Film

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

65 years-old <=

Age-upper limit

100 years-old >

Gender

Male and Female

Key inclusion criteria

Elderly who go to a long-term care facility or enter

Key exclusion criteria

Those who the researcher deems inappropriate

Target sample size

200


Research contact person

Name of lead principal investigator

1st name Satoru
Middle name
Last name Iwase

Organization

Saitama Medical University Hospital

Division name

Department of Palliative Medicine

Zip code

350-0495

Address

38 Morohongou, Moroyama cho Iruma-gun, Saitama, Japan

TEL

049-726-1705

Email

siwase@saitama-med.ac.jp


Public contact

Name of contact person

1st name Satoru
Middle name
Last name Iwase

Organization

Saitama Medical University Hospital

Division name

Department of Palliative Medicine

Zip code

350-0495

Address

38 Morohongou, Moroyama cho Iruma-gun, Saitama, Japan

TEL

049-726-1705

Homepage URL


Email

siwase@saitama-med.ac.jp


Sponsor or person

Institute

Saitama Medical University Hospital

Institute

Department

Personal name



Funding Source

Organization

Murata Manufacturing Co., Ltd.

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Institutional Review Board of Saitama Medical University

Address

38 Moro Hongo, Moroyama-cho, Iruma-gun, Saitama

Tel

049-276-2143

Email

rinri@saitama-med.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

2021 Year 05 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

Terminated

Date of protocol fixation

2021 Year 04 Month 13 Day

Date of IRB

2021 Year 05 Month 15 Day

Anticipated trial start date

2021 Year 05 Month 13 Day

Last follow-up date

2022 Year 08 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

2021 Year 03 Month 16 Day

Last modified on

2023 Year 09 Month 27 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000049736


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name