UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000045117
Receipt number R000051541
Scientific Title The survey of motor ability for the people who had been infected with COVID-19
Date of disclosure of the study information 2021/08/11
Last modified on 2022/02/21 20:54:43

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Basic information

Public title

The survey of motor ability for the people who had been infected with COVID-19

Acronym

The survey of motor ability for the patients with COVID-19

Scientific Title

The survey of motor ability for the people who had been infected with COVID-19

Scientific Title:Acronym

The survey of motor ability for the patients with COVID-19

Region

Japan


Condition

Condition

COVID-19 infection

Classification by specialty

Medicine in general Orthopedics

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To investigate whether patients been infected with COVID-19 have prolonged locomotor dysfunction or persistent musculoskeletal pain, and find the relationship with the status of return to social life

Basic objectives2

Others

Basic objectives -Others

The related factors for prolonged locomotor dysfunction

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The prevalence of locomotive syndrome and the severity

Key secondary outcomes

persistent musculoskeletal pain, the status of return to social life (work, school, sports)


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

20 years-old <=

Age-upper limit

84 years-old >=

Gender

Male and Female

Key inclusion criteria

The patients who had been finished the treatment for COVID-19 and discharged over two months before

Key exclusion criteria

The patients who do not agree with the prescribed opt-out
The patients who are in postoperative acute phase and hard to receive telephone-based medicine

Target sample size

800


Research contact person

Name of lead principal investigator

1st name Akira
Middle name
Last name Sakawa

Organization

Osaka City Juso Hospital

Division name

Department of Orthopedic surgery

Zip code

5320034

Address

2-12-27, Nonakakita, Yodogawa-ku, Osaka, Japan

TEL

0661508000

Email

Akirasakawa@aol.com


Public contact

Name of contact person

1st name Kazunori
Middle name
Last name Hayashi

Organization

Osaka City Juso Hospital

Division name

Department of Orthopedic surgery

Zip code

5320034

Address

2-12-27, Nonakakita, Yodogawa-ku, Osaka, Japan

TEL

0661508000

Homepage URL


Email

kh_ocg@yahoo.co.jp


Sponsor or person

Institute

Osaka City Juso Hospital

Institute

Department

Personal name



Funding Source

Organization

None

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

Osaka City Juso Hospital

Address

2-12-27, Nonakakita, Yodogawa-ku, Osaka, Japan

Tel

0661508000

Email

close to public


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

大阪市立十三市民病院


Other administrative information

Date of disclosure of the study information

2021 Year 08 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

Enrolling by invitation

Date of protocol fixation

2021 Year 08 Month 06 Day

Date of IRB

2021 Year 08 Month 06 Day

Anticipated trial start date

2021 Year 08 Month 06 Day

Last follow-up date

2022 Year 07 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

The survey is conducted by questionnaire


Management information

Registered date

2021 Year 08 Month 10 Day

Last modified on

2022 Year 02 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000051541


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name