TCM Cohort for Elderly COPD
19. august 2026 opdateret af: Henan University of Traditional Chinese Medicine
A Prospective Traditional Chinese Medicine Cohort Study of Chronic Obstructive Pulmonary Disease in the Elderly
This study evaluates the real-world clinical efficacy of traditional Chinese medicine (TCM) in elderly Chronic obstructive pulmonary disease (COPD) patients and explores syndrome characteristics and their associations with biomarkers.
Studieoversigt
Status
Ikke rekrutterer endnu
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
This prospective cohort study, with TCM as the exposure, will enroll 2,386 elderly COPD patients for a 1-year follow-up. The primary evaluation uses the annual acute exacerbation rate as the outcome to evaluate the clinical efficacy of TCM. In addition, the study will investigate the characteristics of TCM syndromes.
Based on the cohort, we will collect peripheral blood, exhaled breath condensate, sputum, and tongue coating samples from 200 elderly COPD patients with four typical TCM syndromes, 200 non-elderly COPD patients with corresponding syndromes, and 50 healthy volunteers. Multi-omics approaches will be used to identify TCM syndrome-related biomarkers.
Undersøgelsestype
Observationel
Tilmelding (Anslået)
2386
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Haifeng Wang
- Telefonnummer: +86-0371-66207856
- E-mail: wangh_f@126.com
Undersøgelse Kontakt Backup
- Navn: Jiansheng Li
Studiesteder
-
-
Henan
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Zhengzhou, Henan, Kina, 450000
- The First Affiliated Hospital of Henan University of Chinese Medicine
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-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ja
Prøveudtagningsmetode
Ikke-sandsynlighedsprøve
Studiebefolkning
COPD is a common chronic respiratory disease characterized by persistent respiratory symptoms and airflow limitation, with recurrent acute exacerbations and progressive impairment of respiratory function.
Beskrivelse
Inclusion Criteria:
- Patients diagnosed with COPD;
- Age ≥ 60 years old;
- Voluntary participation in this study, and sign the informed consent form.
Exclusion Criteria:
- Patients with various mental illnesses or other conditions that prevent normal communication;
- Patients with a history of pulmonary surgery, such as lung volume reduction surgery or lung transplantation;
- Patients with confirmed human immunodeficiency virus infection or acquired immunodeficiency syndrome.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
|---|---|
|
Traditional Chinese Medicine cohort
Regulated use of Chinese medicine treatment protocols is included as an exposure factor.
|
According to the standardised use of TCM protocols, the group is divided into an exposed group (TCM cohort) and an unexposed group (non-TCM cohort).
|
|
Non-Traditional Chinese Medicine cohort
Other elderly COPD patients who do not meet the inclusion criteria for traditional Chinese medicine cohort, are classified into the non-traditional Chinese medicine cohort.
|
Alle interventionsforanstaltninger, der ikke opfylder kriterierne for TCM-eksponering, betragtes som ikke-TCM-eksponering.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Annual acute exacerbation rate
Tidsramme: Up to week 52.
|
The annual acute exacerbation rate will be calculated in each group at the end of the trial.
|
Up to week 52.
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Forced Vital Capacity (FVC)
Tidsramme: Evaluate the FVC at weeks 26 and 52.
|
FVC will be applied to assess pulmonary function.
|
Evaluate the FVC at weeks 26 and 52.
|
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Forced Expiratory Volume in One Second (FEV1)
Tidsramme: Evaluate the FEV1 at weeks 26 and 52.
|
FEV1 will be applied to assess pulmonary function.
|
Evaluate the FEV1 at weeks 26 and 52.
|
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FEV1/FVC Ratio
Tidsramme: Evaluate the FEV1/FVC Ratio at weeks 26 and 52.
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FEV1/FVC Ratio will be applied to assess pulmonary function.
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Evaluate the FEV1/FVC Ratio at weeks 26 and 52.
|
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6-Minute Walk Distance (6MWD)
Tidsramme: Evaluate the 6MWD at weeks 26 and 52.
|
The 6MWD will be applied to evaluate the exercise capacity.
The higher values indicate the better exercise capacity.
|
Evaluate the 6MWD at weeks 26 and 52.
|
|
COPD Assessment Test (CAT) Score
Tidsramme: Evaluate the CAT Score at weeks 13, 26, 39 and 52.
|
The CAT score is a questionnaire used to evaluate the impact of COPD on patients' health status, which includes eight items: cough, phlegm, chest tightness, breathlessness, activity limitation, confidence in leaving home, sleep, and energy.
The total CAT score ranges from 0 to 40, with higher scores indicating a greater disease burden and poorer health status.
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Evaluate the CAT Score at weeks 13, 26, 39 and 52.
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Modified Medical Research Council (mMRC) Dyspnea Scale
Tidsramme: Evaluate the mMRC at weeks 13, 26, 39 and 52.
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The mMRC is a scale used to evaluate the severity of dyspnea in patients, which consists of a single item with five grades ranging from 0 to 4. Higher grades indicate more severe dyspnea and greater limitations in daily activities.
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Evaluate the mMRC at weeks 13, 26, 39 and 52.
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St. George's respiratory questionnaire (SGRQ) total scores
Tidsramme: Evaluate the SGRQ Score at weeks 13, 26, 39 and 52.
|
The SGRQ is a scale used to evaluate the quality of life of patients, which includes three dimensions: symptoms, mobility, and the impact of disease on daily life, with a total of 50 items.
The total score range of SGRQ is usually between 0 and 100, with higher scores leading to poorer quality of life.
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Evaluate the SGRQ Score at weeks 13, 26, 39 and 52.
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Anslået)
20. august 2026
Primær færdiggørelse (Anslået)
31. december 2029
Studieafslutning (Anslået)
28. februar 2030
Datoer for studieregistrering
Først indsendt
19. august 2026
Først indsendt, der opfyldte QC-kriterier
19. august 2026
Først opslået (Faktiske)
21. august 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
21. august 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
19. august 2026
Sidst verificeret
1. august 2026
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
- Patologiske processer
- Kronisk sygdom
- Sygdomsegenskaber
- Luftvejssygdomme
- Lungesygdomme
- Lungesygdomme, obstruktiv
- Patologiske tilstande, tegn og symptomer
- Lungesygdom, kronisk obstruktiv
- Terapeutik
- Komplementære terapier
- Medicin, østasiatiske traditionelle
- Medicin, traditionel
- Medicin, kinesisk traditionel
Andre undersøgelses-id-numre
- Cohort for Elderly COPD
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