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Application of computerized cognitive behavioral therapy to improve symptom clusters in patients with chronic obstructive pulmonary disease

Application of computerized cognitive behavioral therapy to improve symptom clusters in patients with chronic obstructive pulmonary disease

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075064
Enrollment
Unknown
Registered
2023-08-24
Start date
2023-09-01
Completion date
Unknown
Last updated
2023-08-28

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

Control group:1. Inside the hospital: routine education, and establish the basis of nursing outside the hospital
2. Outside the hospital: collecting patients' difficult questions related to symptom clusters every week and answering them in the form of meetings.
Experimental group:On the basis of routine health education, patients in the experimental group received 6 times of computerized cognitive behavioral therapy intervention, respectively before the inte

Sponsors

the First Hospital of Shanxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria of COPD revised by the Chinese Respiratory Society in 2021 (including patients with cor pulmonale, respiratory failure below grade ?, and non-invasive mechanical ventilation); 2. Age =40 years old and < 80 years old; 3.0-10 numerical rating scale (NRS) (dyspnea, insomnia, fatigue) screening each symptom =1 points, Hospital anxiety and Depression scale (HADS) : 8 =HADS=15 points; 4. Simple use of smart phones and other modern mobile devices; 5. Clear consciousness, primary school or above education level, logical thinking and communication skills are normal, with reading and writing ability; 6. Informed consent was obtained from patients and their families.

Exclusion criteria

Exclusion criteria: 1. Patients with pulmonary encephalopathy, malignant tumors, etc. 2. Patients with severe mental illness or alcohol or drug dependence; 3. Are participating or have participated in other investigators.

Design outcomes

Primary

MeasureTime frame
Sleep status;Degree of fatigue;Level of depression;Degree of dyspnea;Self-Rating Anxiety Scale;

Secondary

MeasureTime frame
A 6-minute walk test was performed;

Countries

China

Contacts

Public ContactLi Yuling

The First Hospital of Shanxi Medical University

liyuling5646@163.com+86 151 1030 2111

Outcome results

None listed

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