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Trial registered on ANZCTR
Registration number
ACTRN12608000126314
Ethics application status
Approved
Date submitted
3/03/2008
Date registered
10/03/2008
Date last updated
6/11/2009
Type of registration
Retrospectively registered
Titles & IDs
Public title
To investigate the benefit of cycling and flat-ground walking in people with Chronic Obstructive Pulmonary Disease (COPD)
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Scientific title
Evaluation of the physiological and psychological benefits of cycling and flat-ground walking training in people with Chronic Obstructive Pulmonary Disease (COPD): A randomised, single blind trial
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
chronic obstructive pulmonary disease (COPD)
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Condition category
Condition code
Respiratory
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Chronic obstructive pulmonary disease
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Randomised, controlled;
People will be randomly allocated into one of two groups.
The first group is flat-ground walking group
People in this group will be trained in the rehabilitation gym, walking around a rectanglar track starting from 30 minutes and gradually increase up to 45 minutes by week 6. The training will go for 8 weeks, 3 times per week. The walking speed of each individual is based on their incremental shuttle walk test result (75% of their peak walking speed). We aim to increase their walking speed according to their exercise tolerance each week.
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Intervention code [1]
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Rehabilitation
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Comparator / control treatment
People will be randomly allocated into one of two groups.
The second group is cycling group
People in this group will be trained in the rehabilitation gym with a stationary bike, starting with 30 minutes training and gradually increase up to 45 minutes. The initial intensity is set at 60% of their peak work rate achieved in the incremental cycle test. The training will go for 8 weeks, three times per week. We aim to increase their exercise intensity according to their exercise tolerance each week.
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Control group
Active
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Outcomes
Primary outcome [1]
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Functional exercise capacity - assessed by the incremental shuttle walk test and the endurance shuttle walk test
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Assessment method [1]
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Timepoint [1]
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At baseline and at 8 weeks
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Primary outcome [2]
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Health related quality of life - assessed by chronic respiratory disease questionnaire
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Assessment method [2]
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Timepoint [2]
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At baseline and at 8 weeks
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Secondary outcome [1]
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Exercise capacity - assessed by the incremental and endurance cycle test
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Assessment method [1]
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Timepoint [1]
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At baseline and at 8 weeks
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Secondary outcome [2]
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Lung function
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Assessment method [2]
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Timepoint [2]
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Measured at baseline only
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Secondary outcome [3]
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Compliance
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Assessment method [3]
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Timepoint [3]
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At the completion of the 8 week intervention
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Secondary outcome [4]
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Acceptability of the training interventions - cycling and flat-ground walking training
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Assessment method [4]
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Timepoint [4]
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At the completion of the 8-week intervention
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Eligibility
Key inclusion criteria
Chronic obstructive pulmonary disease; stable condition; Both male and female participants will be included with no age limits as long as the inclusion crieria are met.
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Minimum age
Not stated
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Maximum age
Not stated
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Unstable cardiac disease, completed a pulmonary rehabilitation program in the last 12 months or attending maintenance exercise, inability to understand English, Body Mass Index (BMI) over or equal to 35 kg/m²
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
participants will be randomised after initial baseline testing by a computer program.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Stratified randomisation using a computer-based program. The stratification is based on the percentage of predicted six-minute walking distance, forced expiratory volume in the first second (FEV1), symptom which limits the peak incremental cycle test performance
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
4/05/2006
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
40
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Recruitment postcode(s) [1]
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2139
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Funding & Sponsors
Funding source category [1]
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Self funded/Unfunded
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Name [1]
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Address [1]
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Country [1]
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Primary sponsor type
University
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Name
The University of Sydney
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Address
University of Sydney
Faculty of Health Sciences
Cumberland Campus C42
75 East St
Lidcombe NSW 2141
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Country
Australia
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Secondary sponsor category [1]
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Hospital
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Name [1]
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Concord Repatriation General Hospital
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Address [1]
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Hospital Road
Concord NSW 2139
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Country [1]
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Concord Hospital (Eastern Zone of Sydney South West Area Health Service Human Research Ethics Committee)
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Ethics committee address [1]
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Concord Repatriation General Hospital
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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Approval date [1]
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13/02/2006
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Ethics approval number [1]
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CH62/6/2005-083-J Alison
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Summary
Brief summary
The aim of the project is to determine whether the benefit of flat-ground walking training is similar to cycling training in improving exercise capacity and health related quality of life (HRQoL) in patients with chronic obstructive pulmonary disease (COPD). Hypothesis: On completion of an eight-week training program, subjects with COPD will demonstrate similar improvement in exercise capacity and HRQoL in the flat-ground walking training group and the cycling grop.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Wai Man Regina Leung
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Address
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Institute of Sports Medicine
Hospital Road
Concord NSW 2139
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Country
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Australia
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Phone
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+ 61 2 97677602
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Associate Professor Jenny Alison
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Address
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Discipline of Physiotherapy
Faculty of Health Sciences
University of Sydney
Cumberland Campus C42
75 East St
Lidcombe NSW 2141
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Country
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Australia
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Phone
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+61 2 93519371
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Fax
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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