Status:
NOT_YET_RECRUITING
Effectiveness and Cost-effectiveness of Digital Psychological Intervention (EmoEase) in Chinese COPD Patients
Lead Sponsor:
Peking Union Medical College
Conditions:
Chronic Obstructive Pulmonary Disease
Depression
Eligibility:
All Genders
35+ years
Phase:
NA
Brief Summary
Background Mental health issues are common and often overlooked in COPD patients. Digital psychological interventions might help, but their effectiveness in Chinese COPD patients hasn't been studied. ...
Detailed Description
Background Mental health problems in chronic obstructive pulmonary disease (COPD) patients are common and frequently neglected. Digital psychological interventions may reduce mental health problems, b...
Eligibility Criteria
Inclusion
- Age 35 years or older;
- Post-bronchodilator FEV1/FVC ≤70% or confirmed COPD patients;
- Literate and able to type;
- Have a smartphone;
- Be proficient in using the WeChat applet;
- Willingness to self-help iCBT sessions for 8 weeks, 10-20 minutes of practice per session, roughly 1 hour per week, time and place flexible;
- Receive three follow-up visits within four months (2 offline, 1 online) and complete a physical exam and online questionnaire; and
- Willingness to provide the hospital with their usual cell phone number.
Exclusion
- Patients with a physician diagnosis of asthma or asthma-COPD overlap syndrome;
- Patients hospitalized for COPD within the previous one year;
- Having severe cognitive dysfunction and being unable to communicate;
- Severely ill with less than 12-month life expectancy.
Key Trial Info
Start Date :
October 1 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
January 30 2026
Estimated Enrollment :
1200 Patients enrolled
Trial Details
Trial ID
NCT06026709
Start Date
October 1 2025
End Date
January 30 2026
Last Update
August 13 2025
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