UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000047581
Receipt number R000054259
Scientific Title Long-term symptoms, complications and social outcomes after COVID-19: a prospective cohort study using a self-administered questionnaire
Date of disclosure of the study information 2022/05/01
Last modified on 2022/10/31 16:23:03

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Basic information

Public title

COVID-19 Recovery Study I

Acronym

CORES I

Scientific Title

Long-term symptoms, complications and social outcomes after COVID-19: a prospective cohort study using a self-administered questionnaire

Scientific Title:Acronym

CORES I

Region

Japan


Condition

Condition

COVID-19

Classification by specialty

Medicine in general Cardiology Pneumology
Psychosomatic Internal Medicine Infectious disease Emergency medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate long-term symptoms and complications of patients hospitalized and discharged alive after a diagnosis of COVID-19

Basic objectives2

Others

Basic objectives -Others

Presence of long-term symptoms and complications

Trial characteristics_1

Exploratory

Trial characteristics_2


Developmental phase

Not applicable


Assessment

Primary outcomes

Presence of long-term symptoms and complications at three months, six months, one year, and two years after diagnosis of COVID-19

Key secondary outcomes

Physical and mental health status, socioeconomic status, and quality of life at three months, six months, one year, and two years after diagnosis of COVID-19


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


Not applicable

Gender

Male and Female

Key inclusion criteria

(1) Persons diagnosed with COVID-19 at a medical institution, etc.

(2) Persons 20 years of age or older who were hospitalized and discharged alive from a cooperative research institute in Japan between February and July 2022 for the treatment of 1 above.

Key exclusion criteria

(1) Persons deemed unfit by the physician

(e.g., patients who have difficulty communicating in Japanese or cooperating in surveys)

Target sample size

3000


Research contact person

Name of lead principal investigator

1st name Hiroyasu
Middle name
Last name Iso

Organization

National Center for Global Health and Medicine

Division name

Institute for Global health Policy Research, Bureau of International Health Cooperation

Zip code

162-8655

Address

1-21-1, Toyama Shinjuku-ku, Tokyo, Japan

TEL

03-3202-7181

Email

hiso@it.ncgm.go.jp


Public contact

Name of contact person

1st name Mariko
Middle name
Last name Hosozawa

Organization

National Center for Global Health and Medicine

Division name

Institute for Global health Policy Research, Bureau of International Health Cooperation

Zip code

162-8655

Address

1-21-1, Toyama Shinjuku-ku, Tokyo, Japan

TEL

03-3202-7181

Homepage URL


Email

mhosozawa@it.ncgm.go.jp


Sponsor or person

Institute

National Center for Global Health and Medicine

Institute

Department

Personal name



Funding Source

Organization

Ministry of Health, Labour and Welfare

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

IRB, National Center for Global Health and Medicine

Address

1-21-1, Toyama Shinjuku-ku, Tokyo, Japan

Tel

03-3202-7181

Email

rinrijm@hosp.ncgm.go.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

独立行政法人地域医療推進機構北海道病院(北海道)、国立病院機構北海道医療センター(北海道)、横浜市立大学附属病院(神奈川県)、聖マリアンナ医科大学横浜市西部病院(神奈川県)、聖マリアンナ医科大学(神奈川県)


Other administrative information

Date of disclosure of the study information

2022 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

No longer recruiting

Date of protocol fixation

2022 Year 04 Month 11 Day

Date of IRB

2022 Year 02 Month 14 Day

Anticipated trial start date

2022 Year 05 Month 01 Day

Last follow-up date

2024 Year 07 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

This is a prospective cohort study of patients hospitalized and discharged alive from collaborative research institutes with COVID-19 between February and July 2022. A self-administered questionnaire will be used to examine long-term symptoms and complications associated with COVID-19, physical and mental health status, and socioeconomic status.


Management information

Registered date

2022 Year 04 Month 25 Day

Last modified on

2022 Year 10 Month 31 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000054259


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name