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COPD-EXA-REHAB. Early Pulmonary Rehabilitation of Patients With Acute Exacerbation of COPD

Primary Purpose

Chronic Obstructive Lung Disease

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Pulmonary rehabilitation
Sponsored by
University Hospital, Gentofte, Copenhagen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Chronic Obstructive Lung Disease focused on measuring COPD, Exacerbation, Rehabilitation

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients admitted to hospital with acute exacerbation of COPD to Department Respiratory Medicine, Gentofte Hospital
  • Verified diagnosis of COPD FEV1/FVC <70 % in stable phase.
  • Expected discharge to their own home.
  • Minimal of 10 meters walking distance independently
  • Oral and written consent
  • Age > 18 year

Exclusion Criteria:

  • Life expectancy <6 months due to another illness (cancer, severe heart disease, etc.)
  • Difficulties in understanding and speaking Danish (eg. due to dementia)
  • Place of residence outside Gentofte Hospital admission area

Sites / Locations

  • Dept. of Respiratory medicine, UH Gentofte

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Standard care group

Rehabilitation group

Arm Description

Standard medical treatment for the exacerbation of COPD Standard medical treatment of COPD according to GOLD A visit by a pulmonary nurse at the patients own home 3-5 days after discharge. Lung function and smoking history is recorded. Correct use of inhaler is instructed. Visit in the outpatient clinic within the next 2-6 months after discharge as follow-up In the outpatient clinic they will receive an offer of pulmonary rehabilitation

The group will begin pulmonary rehabilitation during hospital admission. Afterwards a rehabilitation program twice weekly for 7 weeks. Beside rehabilitation they will receive same treatment as the standard care group

Outcomes

Primary Outcome Measures

Composite outcome of 1 year mortality or hospital readmission
It is all cause mortality in 12 months follow-up period.. Readmission is the proportion of patients with at least 1 hospital readmission in 12 months follow-up period. Intention-to-treat analysis.Secondarily per-protocol analysis.

Secondary Outcome Measures

All cause mortality and time to death
All cause hospital readmission and time to readmission
Proportion of patients with at least 1 hospital readmission of any cause
Hospital readmission by respiratory cause
Health related quality of life
Measured by COPD Assessment TEST (CAT)
Dyspnea
Measured by Medical Respiratory Council (MRC) dyspnea scale
Exercise performance
Composite measure by Incremental Shuttle Walk Test (ISWT) and Endurance Shuttle Walk Test (ESWT)

Full Information

First Posted
December 6, 2016
Last Updated
November 19, 2019
Sponsor
University Hospital, Gentofte, Copenhagen
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1. Study Identification

Unique Protocol Identification Number
NCT02987439
Brief Title
COPD-EXA-REHAB. Early Pulmonary Rehabilitation of Patients With Acute Exacerbation of COPD
Official Title
COPD-EXA-REHAB. Early Pulmonary Rehabilitation of Patients With Acute Exacerbation of COPD
Study Type
Interventional

2. Study Status

Record Verification Date
November 2019
Overall Recruitment Status
Completed
Study Start Date
November 2013 (Actual)
Primary Completion Date
December 2018 (Actual)
Study Completion Date
December 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital, Gentofte, Copenhagen

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Purpose: In a randomized controlled trial we will assess the effect of early pulmonary rehabilitation in patient with an acute exacerbation of chronic obstructive lung disease (AECOPD).
Detailed Description
Background: Pulmonary rehabilitation is a key element in treatment of stable COPD. A Cochrane review from 2011 showed that early pulmonary rehabilitation for COPD exacerbation 6-10 days after discharge, or during prolonged hospitalization significantly reduced mortality and hospitalizations without serious side effects. It consist of 9 small studies and larger RCT studies is required to establish the effect of early pulmonary rehabilitation. AIM: The aim of the study is to investigate whether early pulmonary rehabilitation can reduce mortality og hospitalization in patients with acute exacerbation of COPD. Secondary increase exercise capacity, reduce symptoms and improve quality of life. Methods: Design: The study is a single center randomized, controlled, open label trial, with an intervention group and a control group. The patients are randomized to either a prespecified rehabilitation program, which is standardized to patients with COPD, or usual care. The patients' data are being recorded at baseline and visits at 2 and 6 months: Lung function (FEV1, FVC), CO in exhaled air, O2 saturation in the blood (and possibly O2 supplement), Heart Rate, Dyspnoea (Borg scale and Medical Research Council (MRC scale)), Quality of life (CAT), Walk Test (ISWT and ESWT), Daily medication, Outdoor activity. Information on mortality, hospital admissions, emergency room visits after 6 and 12 months is obtained from relevant databases. Population: Patients Hospitalized with an exacerbation of COPD to the department of respiratory medicine at Gentofte Hospital. The inclusion criteria are: A diagnose of COPD, Age >18, expected discharge to own homes, can walk 10 meters independently (with or without a walking aid). Exclusion criteria are: Life expectancy <6 months due to another illness (cancer, severe heart disease, etc.), difficulties in understanding and speaking Danish (e.g. due to dementia), place of residence outside Gentofte Hospital admission area. Randomization: A total of 150 COPD patients will be included. The participants are randomized to early rehabilitation or usual care in a 1:1 ratio, using a computer-generated block-randomization for each center. The participant is presented with a sealed envelope containing a piece of paper with either "A" (= REHAB) or "B" (= usual care). The randomization list is stored at Gentofte Hospital in a sealed envelope. A participant who is readmitted will not be re-randomized. Patients arre introduced to an acute telephone hotline, operated by a nurse. The patients in the intervention group will during Hospitalization begin the rehabilitation program. The program consist of exercise training, breathing techniques and education. Before discharge the patients will be assessed to either A: outpatient rehabilitation in hospital or community clinic or B: Rehabilitation in their own homes twice weekly in 7 weeks

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Lung Disease
Keywords
COPD, Exacerbation, Rehabilitation

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
150 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard care group
Arm Type
No Intervention
Arm Description
Standard medical treatment for the exacerbation of COPD Standard medical treatment of COPD according to GOLD A visit by a pulmonary nurse at the patients own home 3-5 days after discharge. Lung function and smoking history is recorded. Correct use of inhaler is instructed. Visit in the outpatient clinic within the next 2-6 months after discharge as follow-up In the outpatient clinic they will receive an offer of pulmonary rehabilitation
Arm Title
Rehabilitation group
Arm Type
Experimental
Arm Description
The group will begin pulmonary rehabilitation during hospital admission. Afterwards a rehabilitation program twice weekly for 7 weeks. Beside rehabilitation they will receive same treatment as the standard care group
Intervention Type
Other
Intervention Name(s)
Pulmonary rehabilitation
Intervention Description
The intervention is pulmonary rehabilitation
Primary Outcome Measure Information:
Title
Composite outcome of 1 year mortality or hospital readmission
Description
It is all cause mortality in 12 months follow-up period.. Readmission is the proportion of patients with at least 1 hospital readmission in 12 months follow-up period. Intention-to-treat analysis.Secondarily per-protocol analysis.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
All cause mortality and time to death
Time Frame
12 months
Title
All cause hospital readmission and time to readmission
Description
Proportion of patients with at least 1 hospital readmission of any cause
Time Frame
12 months
Title
Hospital readmission by respiratory cause
Time Frame
12 months
Title
Health related quality of life
Description
Measured by COPD Assessment TEST (CAT)
Time Frame
6 months
Title
Dyspnea
Description
Measured by Medical Respiratory Council (MRC) dyspnea scale
Time Frame
6 months
Title
Exercise performance
Description
Composite measure by Incremental Shuttle Walk Test (ISWT) and Endurance Shuttle Walk Test (ESWT)
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients admitted to hospital with acute exacerbation of COPD to Department Respiratory Medicine, Gentofte Hospital Verified diagnosis of COPD FEV1/FVC <70 % in stable phase. Expected discharge to their own home. Minimal of 10 meters walking distance independently Oral and written consent Age > 18 year Exclusion Criteria: Life expectancy <6 months due to another illness (cancer, severe heart disease, etc.) Difficulties in understanding and speaking Danish (eg. due to dementia) Place of residence outside Gentofte Hospital admission area
Facility Information:
Facility Name
Dept. of Respiratory medicine, UH Gentofte
City
Hellerup
ZIP/Postal Code
DK-2900
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
No

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COPD-EXA-REHAB. Early Pulmonary Rehabilitation of Patients With Acute Exacerbation of COPD

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