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Efficacy of cognitive behavioural therapy and/or simulation-based learning resources on the mental health of chronic obstructive pulmonary disease patients.

Not Applicable
Completed
Conditions
Chronic obstructive pulmonary disease
Anxiety
Depression
Respiratory - Chronic obstructive pulmonary disease
Mental Health - Anxiety
Mental Health - Depression
Registration Number
ACTRN12616001039471
Lead Sponsor
Edith Cowan University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
192
Inclusion Criteria

1) A confirmed diagnosis of COPD by respiratory physicians
2) A positive screen for anxiety and/or depression on the BAI and BDI-II, respectively.

Exclusion Criteria

1) Life expectancy of less than six months
2) Currently involved in another research study
3) An illness exacerbation resulting in hospitalisation within the previous month
4) Diagnosis of dementia
5) Known difficulty with either their eye-sight, fluency in English or filling out self-report measures.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Beck Anxiety Inventory (BAI)[A week after the completion of the intervention (post-intervention) and 3, 6 , 9 and 12 months post-intervention.];Beck Depression Inventory (BDI-II)[A week after the completion of the intervention (post-intervention) and 3, 6 , 9 and 12 months post-intervention.]
Secondary Outcome Measures
NameTimeMethod
St George's Respiratory Questionnaire - quality of life[A week after the completion of the intervention (post-intervention) and 3, 6 , 9 and 12 months post-intervention.];Hospital utilisation by self report (this was decided prospectivelyl)[One year post-intervention];Cost effectiveness of intervention by economic analysis. This will be completed from data linkage to hospital records and Western Australian costs for emergency presentation and hospital admissions at the time of the hospital utilisation.[One year post-intervention];All cause hospitalisations by data linkage to medical records (this was decided during the trial)[Two years pre-intervention and one year post-intervention];Hospital and Anxiety Depression Scale (HAD-S)[A week after the completion of the intervention (post-intervention) and 3, 6 , 9 and 12 months post-intervention.]
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