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Admission and discharge care bundles for COPD

An evaluation of the effectiveness of ‘care bundles’ as a means of improving hospital care and reducing hospital readmission for patients with chronic obstructive pulmonary disease (COPD)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN13022442
Enrollment
76
Registered
2015-02-11
Start date
2015-02-01
Completion date
Unknown
Last updated
2023-03-20

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

Conditions

Topic: Respiratory disorders

Interventions

The intervention is the delivery of a COPD care bundle at either the point of admission to or discharge from hospital.

Sponsors

University of Bristol
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. People over 18 years of age admitted to an acute hospital with COPD 2. Primary cause of admission is COPD (ICD10 diagnostic codes J41-44) Target Gender: Male & Female ; Lower Age Limit 18 years

Exclusion criteria

Exclusion criteria: 1. People admitted to hospital with COPD where this is not the primary cause of admission 2. Elective admissions for COPD

Design outcomes

Primary

MeasureTime frame
COPD re-admission rates; Timepoint(s): 28 days post-discharge

Secondary

MeasureTime frame
1. Compliance with delivery of COPD care bundles; Timepoint(s): 12 months pre- and post- 2. COPD re-admission rates; Timepoint(s): 90-days post-hospital discharge 3. Costs of in-patient medications and procedures; Timepoint(s): 12 months pre-and post- 4. In-hospital mortality; Timepoint(s): 12-months pre- and post- 5. Length of stay for patients with COPD; Timepoint(s): at end of 12-month data collection 6. Mortality; Timepoint(s): 90-day post-hospital discharge 7. Overall re-admission rates; Timepoint(s): 28-days post-hospital discharge 8. Time taken to deliver COPD care bundles; Timepoint(s): post-admission or pre-discharge 9. Total number of COPD admissions; Timepoint(s): monthly 10. Total number of patients for whom COPD care bundle used; Timepoint(s): 12-months post-hospital data collection As with the primary outcome, the secondary outcomes of the study will be measured for a 12-month period pre-and post- a particular index date. This index date is the date upon which an individual implementation site i.e. NHS Trust began to deliver its COPD care bundle or, in the case of comparator sites, the date upon which an individual site's matched implementation site began to deliver its COPD care bundle. This approach will ensure that data are collected during the same ‘before’ and ‘after’ period for matched implementation and comparator sites. 12/12/2016: "Patient and carer experience; Timepoint(s): at end of 12-month data collection" outcome removed from April 2016 protocol.

Countries

England, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 2, 2026