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The COPD Breathlessness Manual: Cognitive-behavioural manual versus information booklets on health service use, mood and health status in patients with chronic obstructive pulmonary disease (COPD)

The COPD Breathlessness Manual: A randomised controlled trial to test a cognitive-behavioural manual versus information booklets on health service use, mood and health status in patients with chronic obstructive pulmonary disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN63986906
Enrollment
200
Registered
2014-05-01
Start date
2010-08-01
Completion date
Unknown
Last updated
2017-02-27

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

Conditions

Chronic Obstructive Pulmonary Disease Respiratory Chronic Obstructive Pulmonary Disease

Interventions

Participants will be randomised to receive either The COPD Breathlessness Manual: A cognitive behavioural guided self help manual or COPD information booklets. They will be guided through their interv

Sponsors

Central & North West London NHS Foundation Trust (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. A diagnosis of COPD 2. A self-rating of breathlessness on the Medical Research Council (MRC) dyspnoea scale of 3,4 or 5 3. Willingness to participate 4. Ability to provide informed consent 5. Ability to read and write in English or with assistance

Exclusion criteria

Exclusion criteria: 1. Known psychosis and personality disorders 2. Receiving psychological therapy 3. Participating in Pulmonary Rehabilitation or within the previous six months 4. Cognitive impairment, dementia 5. Verbal and/or written communication problems

Design outcomes

Primary

MeasureTime frame
The change in the number of A&E attendances over a 12 month period from pre to post intervention.

Secondary

MeasureTime frame
The change in number of hospital admissions, number of hospital bed days, anxiety, depression and health status pre and post intervention. Mood and health status were collected with questionnaires at timepoints baseline, 6 weeks and 6 months.

Countries

United Kingdom

Outcome results

None listed

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