Skip to content

Qualitative study on the psychological change process of patients with COPD combined with anxiety and depression, as well as their psychological and behavioral characteristics and coping strategies in facing pulmonary rehabilitation

Qualitative study on the psychological change process of patients with COPD combined with anxiety and depression, as well as their psychological and behavioral characteristics and coping strategies in facing pulmonary rehabilitation

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500110375
Enrollment
Unknown
Registered
2025-10-13
Start date
2025-04-03
Completion date
Unknown
Last updated
2025-10-20

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

Conditions

chronic obstructive pulmonary disease

Interventions

Interview group on psychological feelings and emotional coping of COPD patients with anxiety and depression:None
Interview Group on Psychological and Behavioral Characteristics of Pulmonary Rehabilitation in COPD Patients with Anxiety and Depression:None

Sponsors

Beijing Chaoyang Hospital Affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 100 Years

Inclusion criteria

Inclusion criteria: (1) Meets the diagnostic criteria in the "Guidelines for the Diagnosis and Treatment of Chronic Obstructive Pulmonary Disease" (revised in 2021) ; (2) Patients with positive results on the HADS scale, i.e. scores >= 8 on the anxiety or depression scale; (3) The patient is conscious and able to independently or with the assistance of the researcher fill out the required research questionnaire; (4) Voluntarily participate in this study and sign an informed consent form; (5) The research subjects are aware of their own disease diagnosis.

Exclusion criteria

Exclusion criteria: (1) Patients with severe complications or other serious chronic diseases affecting the study; (2) Individuals with hearing and/or speech impairments; (3) Family members do not agree with the patient's participation in this study; (4) Patients who have participated in other studies and have affected the implementation and accuracy of the results of this study. (5) During the research process, the investigator withdrew due to various reasons, including difficulty breathing and inability to continue communicating, unwillingness to cooperate with the study, etc.

Design outcomes

Primary

MeasureTime frame
Hospital Anxiety and Depression Scale,HADS;

Secondary

MeasureTime frame
General Information Survey Form;

Countries

China

Contacts

Public ContactYanrui Jia

Beijing Chaoyang Hospital Affiliated to Capital Medical University

13910707075@139.com+86 139 1070 7075

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026