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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT04217330




Registration number
NCT04217330
Ethics application status
Date submitted
17/12/2019
Date registered
3/01/2020

Titles & IDs
Public title
An Implementation Trial to Improve Access to Pulmonary Rehabilitation in People With COPD
Scientific title
HomeBase2: An Implementation Trial to Improve Access to Pulmonary Rehabilitation in People With Chronic Obstructive Pulmonary Disease
Secondary ID [1] 0 0
55803
Universal Trial Number (UTN)
Trial acronym
HomeBase2
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Chronic Obstructive Pulmonary Disease 0 0
Condition category
Condition code
Respiratory 0 0 0 0
Chronic obstructive pulmonary disease

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
BEHAVIORAL - Choice of home-based or centre-based pulmonary rehabilitation
BEHAVIORAL - Centre-based pulmonary rehabilitation

Experimental: Intervention - Pulmonary rehabilitation programs assigned to the intervention group will offer eligible participants the choice of participating in an 8-week program of either home-based pulmonary rehabilitation or traditional centre-based pulmonary rehabilitation.

Active comparator: Control - Pulmonary rehabilitation programs assigned to the control group will offer eligible participants the opportunity to participate in an 8-week centre-based pulmonary rehabilitation program, as per current practice.


BEHAVIORAL: Choice of home-based or centre-based pulmonary rehabilitation
Participants will be offered the choice of HomeBase, a home-based pulmonary rehabilitation program, or the traditional centre-based pulmonary rehabilitation program.

BEHAVIORAL: Centre-based pulmonary rehabilitation
Participants will be offered a traditional centre-based pulmonary rehabilitation program
Intervention code [1] 0 0
BEHAVIORAL
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
All cause, non-elective hospitalisation
Timepoint [1] 0 0
12 months after completing pulmonary rehabilitation
Secondary outcome [1] 0 0
Change in 6-minute walk distance
Timepoint [1] 0 0
End of rehabilitation and 12 months later
Secondary outcome [2] 0 0
Change in chronic respiratory disease questionnaire total and domain scores
Timepoint [2] 0 0
End of rehabilitation and 12 months later
Secondary outcome [3] 0 0
EQ-5D-5L
Timepoint [3] 0 0
End of rehabilitation and 12 months later
Secondary outcome [4] 0 0
Change in dyspnoea-12
Timepoint [4] 0 0
End of rehabilitation and 12 months later
Secondary outcome [5] 0 0
Change in objectively measured physical activity
Timepoint [5] 0 0
End of rehabilitation and 12 months later
Secondary outcome [6] 0 0
Health care costs
Timepoint [6] 0 0
12 months following pulmonary rehabilitation completion
Secondary outcome [7] 0 0
Program completion
Timepoint [7] 0 0
End of rehabilitation

Eligibility
Key inclusion criteria
Inclusion criteria for pulmonary rehabilitation programs:

• Outpatient pulmonary rehabilitation programs that admit at least 50 people with COPD each year.

Inclusion criteria for participants:

* Diagnosis of COPD confirmed on spirometry
* Able to read, write and speak English
* Able to provide informed consent.
Minimum age
No limit
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
* Attended pulmonary rehabilitation within 1 year
* Comorbidities which preclude exercise training.

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s

The people assessing the outcomes
Intervention assignment
Parallel
Other design features
Phase
NA
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
1/03/2021
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
1/08/2025
Actual
Sample size
Target
490
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
NSW,NT,QLD,SA,VIC
Recruitment hospital [1] 0 0
Royal Prince Alfred Hospital - Sydney
Recruitment hospital [2] 0 0
Mount Druitt Hospital - Sydney
Recruitment hospital [3] 0 0
Prince of Wales Hospital - Sydney
Recruitment hospital [4] 0 0
Westmead Hospital - Sydney
Recruitment hospital [5] 0 0
Top End Health Service - Darwin
Recruitment hospital [6] 0 0
Prince Charles Hospital - Brisbane
Recruitment hospital [7] 0 0
Central Adelaide Local Health Network - Adelaide
Recruitment hospital [8] 0 0
Southern Adelaide Local Health Network - Adelaide
Recruitment hospital [9] 0 0
Peninsula Health - Melbourne
Recruitment hospital [10] 0 0
St John of God Frankston Rehabilitation - Melbourne
Recruitment hospital [11] 0 0
Western Health - Melbourne
Recruitment postcode(s) [1] 0 0
2050 - Sydney
Recruitment postcode(s) [2] 0 0
- Sydney
Recruitment postcode(s) [3] 0 0
- Darwin
Recruitment postcode(s) [4] 0 0
4032 - Brisbane
Recruitment postcode(s) [5] 0 0
- Adelaide
Recruitment postcode(s) [6] 0 0
- Melbourne

Funding & Sponsors
Primary sponsor type
Other
Name
Monash University
Address
Country
Other collaborator category [1] 0 0
Other
Name [1] 0 0
Institute for Breathing and Sleep, Australia
Address [1] 0 0
Country [1] 0 0
Other collaborator category [2] 0 0
Other
Name [2] 0 0
University of Melbourne
Address [2] 0 0
Country [2] 0 0
Other collaborator category [3] 0 0
Other
Name [3] 0 0
La Trobe University
Address [3] 0 0
Country [3] 0 0
Other collaborator category [4] 0 0
Other
Name [4] 0 0
Thoracic Society of Australia and New Zealand
Address [4] 0 0
Country [4] 0 0
Other collaborator category [5] 0 0
Other
Name [5] 0 0
Lung Foundation Australia
Address [5] 0 0
Country [5] 0 0

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Anne Holland
Address 0 0
Monash University
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Anne Holland
Address 0 0
Country 0 0
Phone 0 0
+61 3 99030214
Fax 0 0
Email 0 0
[email protected]
Contact person for scientific queries

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
What data in particular will be shared?
The investigators will make individual participant data available to other researchers for related projects with appropriate ethical oversight. The data provided would be in re-identifiable form with no identifying information provided. Access will only be granted to researchers who agree to preserve the confidentiality of the information. Access will require approval from the research team as well as approval from a Human Research Ethics Committee.

Supporting document/s available: Study protocol, Informed consent form (ICF)
When will data be available (start and end dates)?
After publication of the main trial results, for 7 years.
Available to whom?
Access will only be granted to researchers who agree to preserve the confidentiality of the information. Access will require approval from the research team as well as approval from a Human Research Ethics Committee
Available for what types of analyses?
How or where can data be obtained?


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.


Results not provided in https://clinicaltrials.gov/study/NCT04217330