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KOrea COpd Subgroup Registry and Subtype Research

Domestic COPD Patients Registry Business and COPD Phenotype Research Based by Registry Data - Multi-centered Trial

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02800499
Acronym
KOCOSS
Enrollment
2000
Registered
2016-06-15
Start date
2011-12-01
Completion date
2042-12-31
Last updated
2026-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COPD

Brief summary

The KOrea COpd Subgroup Study team (KOCOSS) cohort is an ongoing, longitudinal, prospective, non-interventional and observational study within the Korean COPD patients. The prevalence of early COPD (mild to moderate COPD based by 2011 GOLD(the Global Initiative for Chronic Obstructive Lung Disease) guideline) is high in Korea. However, the patients with early COPD are not underdiagnosed due to mild symptom. The purpose of this study is to investigate early COPD characteristics and disease course and to form a guideline for early detection of COPD patients and prevention of progression to severe COPD.

Detailed description

This study is a multicentered, observational study of the patients with COPD who were enrolled in 45 tertiary and university-affiliated hospitals from December 2012 to now. The initial evaluation for all patients includes pulmonary function tests (PFT), 6-min walk distance (6MWD), COPD Assessment Test (CAT), modified Medical Research Council (mMRC) dyspnea scale, and the COPD-specific version of St. George's Respiratory Questionnaire (SGRQ-C), exacerbations in the previous 12 months, smoking status, patient-reported education level, medications and comorbidities. Pulmonary function tests (PFTs) are performed every 6 months and CAT, mMRC and SGRQ-C are evaluated every 6 months and 6 min walt test is performed every years during the whole period of study. All of the data were reported using case-report forms (CRFs) which are completed by physicians or trained nurses, and the patients are to be evaluated at regular 6-month intervals after the initial examination.

Interventions

None listed

Sponsors

Konkuk University Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Over 40 years old South Korean COPD patients(Bronchodilator test results FEV1/FVC \<0.7) * COPD patients who complain of cough, sputum, dyspnea * Unrelated smoking history

Exclusion criteria

* other disease like asthma patients which is similar to COPD symptoms. * patients who is not suitable for pulmonary function test and communication * myocardial infarction or cerebrovascular event within the previous 3 months * pregnants * patients who disagree with registration * rheumatoid patients * cancer patients(including metastatic cancer, leukemia, lymphoma) * irritable bowel syndrome * patients who use systemic steroids over 8 weeks due to other diseases except COPD

Design outcomes

Primary

MeasureTime frameDescription
Number of acute exacerbation5 yearsNumber of events

Secondary

MeasureTime frameDescription
Pulmonary function tests5 yearsCOPD severity will be assessed based on post-bronchodilator Forced expiratory volume in one second(FEV) and FEV1/FVC(Forced vital capacity). FEV1 to forced vital capacity (FVC) :Mild - FEV1/FVC\<0.7, FEV1 ≥80% normal Moderate - FEV1/FVC\<0.7, FEV1 50-79% normal; Severe - FEV1/FVC\<0.70, FEV1 30-49% normal; Very Severe - FEV1/FVC\<0.70, FEV1 \<30% predicted. We will measure spirometry at screening and every 6 months.
Modified Medical Research Council [mMRC] dyspnea scale5 yearsmMRC dyspnea scale is five-point scale with higher scores indicating more severe dyspnea. We will assess mMRC at screening and every 6 months.
COPD Assessment Test (CAT)5 yearsThe CAT score was also used for evaluation of dyspnea. It consists of 8 items, each scored from 0 to 5, with higher scores indicating a more severe symptom.We will measure CAT at screening and every 6 months.
6-min walk distance (6MWD)5 yearsThe 6MWD has been used as a simple tool to assess overall exercise tolerance in COPD patients. We will measure 6 min walk distance by ATS guideline at screening and every 6 months during the follow-up period
the COPD-specific version of St. George's Respiratory Questionnaire (SGRQ-C)5 yearsto assess the health status from the patient's perspective .The SGRQ-C is a 14-item questionnaire that can be summarized as a total score, as well as by three component scores for symptoms, activities, and impacts. We will assess SGRQ at screening and every 6 months.
Percentage of Participants with smoking history5 yearswe will assess smoking history at screening and every 6 months
Percentage of Participants with Other Relevant Diseases5 yearsWe will examine the relevant disease which is defined as respiratory diseases, cardiovascular diseases (ischaemic heart disease, heart failure, hypertension), and other diseases (osteoporosis, GERD(gastroesophageal reflux disease), hyperlipidemia, bronchiectasis, emphysema).
COPD TreatmentThrough study completion, average 5 yearsCOPD treatments are defined as inhaled therapies, oral therapies and other therapies administered during the enrollment and influenza vaccination and smoking cessation therapy

Countries

South Korea

Contacts

PRINCIPAL_INVESTIGATORKi-Seok NA Jung, Doctor

Hallym University Medical Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 27, 2026