UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000055476
Receipt number R000063387
Scientific Title Cross-education effect of form rolling on the thing muscles in patients after total knee arthroplasty
Date of disclosure of the study information 2024/09/11
Last modified on 2025/03/17 22:24:19

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Basic information

Public title

The acute cross-education effect of foam rolling on the thigh muscles in patients after total knee arthroplasty

Acronym

Cross-education effect of form rolling on the thing muscles in patients after total knee arthroplasty

Scientific Title

Cross-education effect of form rolling on the thing muscles in patients after total knee arthroplasty

Scientific Title:Acronym

Cross-education effect of form rolling on the thing muscles in patients after total knee arthroplasty

Region

Japan


Condition

Condition

total knee arthroplasty

Classification by specialty

Orthopedics Rehabilitation medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Cross-education effects on pain and joint range of motion in patients undergoing total knee arthroplasty

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Pain and knee joint range of motion

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

Self control

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

Foam roller performed on non-surgical thigh for 180 seconds

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

55 years-old <=

Age-upper limit

90 years-old >=

Gender

Male and Female

Key inclusion criteria

Patients who have undergone total knee arthroplasty and have consented to the purpose of this study

Key exclusion criteria

The subjects were those who could not give consent to the purpose of this study and those who had rheumatoid arthritis in their current medical history

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Masanobu
Middle name
Last name Yokochi

Organization

Department of Rehabilitation, Takeda General Hospital

Division name

Department of Rehabilitation

Zip code

965-8585

Address

3-27 Yamagamachi, Aizuwakamatsu, Fukushima

TEL

0242275511

Email

masanobu815@hotmail.com


Public contact

Name of contact person

1st name Masanobu
Middle name
Last name Yokochi

Organization

Takeda General Hospital

Division name

Department of Rehabilitation

Zip code

965-8585

Address

3-27 Yamagamachi, Aizuwakamatsu, Fukushima

TEL

0242275511

Homepage URL


Email

masanobu815@hotmail.com


Sponsor or person

Institute

Takeda General Hospital

Institute

Department

Personal name



Funding Source

Organization

Takeda General Hospital

Organization

Division

Category of Funding Organization

Non profit foundation

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Takeda General Hospital

Address

3-27 Yamagamachi, Aizuwakamatsu, Fukushima

Tel

0242275511

Email

masanobu815@hotmail.com


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 09 Month 11 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

Completed

Date of protocol fixation

2022 Year 11 Month 01 Day

Date of IRB

2022 Year 11 Month 20 Day

Anticipated trial start date

2023 Year 03 Month 01 Day

Last follow-up date

2024 Year 12 Month 01 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 09 Month 10 Day

Last modified on

2025 Year 03 Month 17 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000063387