Skip to content

Education Program for people with Chronic Obstructive Pulmonary Disease

Evaluation of a psychoeducational intervention for people with chronic obstructive pulmonary disease: a mixed methods study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12618001905257
Enrollment
62
Registered
2018-11-22
Start date
2019-08-01
Completion date
2019-12-30
Last updated
2021-06-21

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

Conditions

None listed

Brief summary

The aim of this study is to develop and evaluate the effectiveness of a group psychoeducational intervention on symptoms of anxiety and depression, health-related quality of life and self-efficacy for people with COPD. A pilot single-blind randomised controlled trial will be conducted with randomisation to either a group psychoeducational intervention or usual care. Psychoeducational intervention will be provided to the intervention group, while the control group receive usual care. The psychoeducational intervention is an adaptation of the Stanford Chronic Disease Self-management Program (CDSMP) developed in the United States. It is a six-week interactive workshop for people with chronic obstructive pulmonary disease.Topics of the psychoeducational intervention covered include: 1)techniques to cope with issues like fatigue, isolation and pain; 2) appropriate exercise aiming to maintain and enhance strength, endurance and flexibility; 3) appropriate use of medications; 4) effective communication with health professionals, family and friends; 5) healthy diet; 6) decision making; 7) how to evaluate new treatment.

Interventions

Name: psychoeducational intervention for people with COPD The aims of intervention are to alleviate the symptoms of anxiety and depression and improve health-related quality of life in people with COPD by increasing individuals’ daily self-management skills. The psychoeducational intervention is an adaptation of the Stanford Chronic Disease Self-management Program (CDSMP) developed in the United States. Ruixue Cao, the Phd Candidate of the University of Newcastle, will delivery the intervention.

Name: psychoeducational intervention for people with COPD The aims of intervention are to alleviate the symptoms of anxiety and depression and improve health-related quality of life in people with COPD by increasing individuals’ daily self-management skills. The psychoeducational intervention is an adaptation of the Stanford Chronic Disease Self-management Program (CDSMP) developed in the United States. Ruixue Cao, the Phd Candidate of the University of Newcastle, will delivery the intervention. Her supervisors Prof. Sally Chan and Dr Graeme Browne will provide guidance during the intervention delivery. The psychoeducational intervention is a face to face group intervention, which consisted of weekly action planning, modelling of behaviours, problem solving, interpretation of symptoms, symptoms management techniques, individual decision making and feedback. Topics of psychoeducational intervention covered include: 1)techniques to cope with issues like fatigue, isolation and pain; 2) appropriate exercise aiming to maintain and enhance strength, endurance and flexibility; 3) appropriate use of medications; 4) effective communication with health professionals, family and friends; 5) healthy diet; 6) decision making.The psychoeducational intervention will consist of six weekly, 2.5 hour sessions led by one educator (Ruixue Cao). Each group will consist of up to 12 participants. During the six weeks' intervention, the participants will received message or phone weekly for reminding them to attend the intervention on time. The psychoeducational intervention will be held in a community clinic which is convenient for the participants.

Sponsors

The University of Newcastle
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Educational / counselling / training
Masking
Blinded (masking used) (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Inclusion Criteria • Male or female outpatients aged 18 years and above with a confirmed diagnosis of COPD (FEV1/FVC <0.70). • All levels of COPD severity are eligible including mild to moderate and severe to very severe stage. • Patients are willing to participate in the study and have capacity to provide informed consent. • Agree to follow the study procedures • Speak Mandarin • Able to read and write Chinese

Exclusion criteria

Exclusion criteria • People with cognitive impairment such as dementia • People participated in any other clinical trial

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026