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Trial registered on ANZCTR
Registration number
ACTRN12609000809235
Ethics application status
Approved
Date submitted
11/09/2009
Date registered
17/09/2009
Date last updated
9/07/2012
Type of registration
Retrospectively registered
Titles & IDs
Public title
Exercise for health: A breast cancer recovery project
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Scientific title
Using the telephone to promote exercise-based rehabilitation in regional/rural/remote Australian breast cancer survivors
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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:
Breast cancer
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Condition category
Condition code
Cancer
239970
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0
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Breast
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Intervention group: Half of women recruited into the study will be randomly assigned to a telephone-delivered exercise rehabilitation program and will receive an exercise workbook, an exercise tracker to log their physical activity and telephone support calls over 8 months from a study-trained Exercise Physiologist. Exercise Physiologists will contact participants regularly over 8 months to assist them to progress through their workbook to develop a safe and appropriate exercise regimen (16 calls over 8 months).
The final goal is to have women exercising at least 4 times per week, at moderate intensities, with exercise sessions lasting 45+ minutes. To achieve this goal, the exercise programs will be gradually progressed across the weeks by introducing different types of exercise and slowly increasing their intensity and duration. Progression in exercise will depend on the participant and how she is dealing with the exercises and her breast cancer treatment.
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Intervention code [1]
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Rehabilitation
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Comparator / control treatment
Control group: The other half of women recruited into the study will be randomly assigned to the usual care control group and will participate in all study assessments and receive usual care from their treating clinicians, which generally includes information booklets on recovery following breast cancer treatment. Duration of the intervention is 8 months.
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Control group
Active
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Outcomes
Primary outcome [1]
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Quality of Life using the Functional Assessment of Cancer Therapy for Breast Cancer (FACT-B) instrument
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Assessment method [1]
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Timepoint [1]
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Measured at 3 time points: 4 weeks post breast cancer surgery (baseline), 6 months post-surgery and 12 months post-surgery
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Primary outcome [2]
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Upper body function using the Disability of the Arm, Shoulder and Hand (DASH) instrument
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Assessment method [2]
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Timepoint [2]
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Measured at 3 time points: 4 weeks post breast cancer surgery (baseline), 6 months post-surgery and 12 months post-surgery
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Primary outcome [3]
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Fatigue using the Functional Assessment of Chronic Illness Therapy - Fatigue (FACIT-fatigue) instrument
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Assessment method [3]
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Timepoint [3]
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Measured at 3 time points: 4 weeks post breast cancer surgery (baseline), 6 months post-surgery and 12 months post-surgery
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Primary outcome [4]
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Feasibility measured by the following indicators: Consent rate; % intervention group participants receiving 75% or more of scheduled calls; participant satisfaction ratings
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Assessment method [4]
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Timepoint [4]
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Measured at 12 months post-surgery
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Secondary outcome [1]
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Physical activity levels using the Active Australia Survey and the Community Healthy Activities Models Program for Seniors (CHAMPS) survey
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Assessment method [1]
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Timepoint [1]
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Measured at 3 time points: 4 weeks post breast cancer surgery (baseline), 6 months post-surgery and 12 months post-surgery
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Secondary outcome [2]
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Lymphoedema assessed via self-report questionnaire items
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Assessment method [2]
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Timepoint [2]
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Measured at 3 time points: 4 weeks post breast cancer surgery (baseline), 6 months post-surgery and 12 months post-surgery
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Eligibility
Key inclusion criteria
First diagnosis of breast cancer; residing in a regional, remote or rural area according to the Australian Standard Geographical Classification (2001); willing to accept a random assignment to the control or exercise rehabilitation program group
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Minimum age
20
Years
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Maximum age
69
Years
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Those planning on moving away from current residence during the study period; those pregnant, lactating or planning to fall pregnant during the study period; those planning to have additional surgery during the study period; those who have a medical condition or are taking medications that would prohibit participation in any of the research protocols
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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)
Randomisation by computer after eligibility status determined
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computer generated
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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
1/03/2007
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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
140
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
QLD
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Funding & Sponsors
Funding source category [1]
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Charities/Societies/Foundations
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Name [1]
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National Breast Cancer Foundation
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Address [1]
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Level 3, 18-20 York Street
SYDNEY NSW 2000
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Country [1]
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Australia
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Primary sponsor type
University
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Name
Cancer Prevention Research Centre, School of Population Health, The University of Queensland
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Address
Level 3, Public Health Building
The University of Queensland
Herston Road
Herston QLD 4006
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
237072
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Country [1]
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Behavioural & Social Sciences Ethical Review Committee
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Ethics committee address [1]
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The Ethics Officer Research andResearch Training Division Cumbrae-Stewart Building The University of Queensland ST. LUCIA QLD 4072
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
243748
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Approval date [1]
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06/02/2007
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Ethics approval number [1]
243748
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EC00176
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Ethics committee name [2]
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Toowoomba & Darling Downs Health Service District Human Research Ethics Committee
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Ethics committee address [2]
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Level 2 Cossart House TDDHSD Locked Bag 2 TOOWOOMBA QLD 4350
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Ethics committee country [2]
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Australia
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Date submitted for ethics approval [2]
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Approval date [2]
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14/12/2006
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Ethics approval number [2]
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EC00182
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Ethics committee name [3]
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St Vincent's and Holy Spirit Health
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Ethics committee address [3]
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PO Box 555 SPRING HILL QLD 4004
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Ethics committee country [3]
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Australia
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Date submitted for ethics approval [3]
243751
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Approval date [3]
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08/12/2006
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Ethics approval number [3]
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EC00324
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Ethics committee name [4]
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Rockhampton Health Service District Human Research Ethics Committee
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Ethics committee address [4]
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C/- Executive director of Medical Services Rockhampton Hospital Canning Street ROCKHAMPTON QLD 4700
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Ethics committee country [4]
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Australia
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Date submitted for ethics approval [4]
243752
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Approval date [4]
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08/12/2006
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Ethics approval number [4]
243752
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EC00173
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Ethics committee name [5]
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Royal Brisbane and Women's Hospital Human Research Ethics Committee
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Ethics committee address [5]
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RBWH Human Research Ethics Level 7, Block 7 Royal Brisbane and Women's Hospital Butterfield Street
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Ethics committee country [5]
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Australia
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Date submitted for ethics approval [5]
243753
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Approval date [5]
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16/02/2007
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Ethics approval number [5]
243753
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EC00172
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Ethics committee name [6]
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Greenslopes Private Hospital Human Research Ethics Committee
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Ethics committee address [6]
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Greenslopes Private Hospital Ethics Committee Newdgate Street GREENSLOPES QLD 4120
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Ethics committee country [6]
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Australia
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Date submitted for ethics approval [6]
243754
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Approval date [6]
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13/02/2007
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Ethics approval number [6]
243754
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EC00161
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Ethics committee name [7]
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Cairns & Hinterland Health Service District Ethics Committee
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Ethics committee address [7]
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Cairns & Hinterland Health Service District HREC Cairns Base Hospital PO Box 902 CAIRNS QLD 4870
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Ethics committee country [7]
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Australia
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Date submitted for ethics approval [7]
243755
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Approval date [7]
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01/03/2007
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Ethics approval number [7]
243755
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EC00157
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Ethics committee name [8]
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Mater Health Services Human Research Ethics Committee
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Ethics committee address [8]
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Mater Health Services Research Ethics Room 235, Level 2, Aubigny Place Raymond Terrace SOUTH BRISBANE QLD 4101
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Ethics committee country [8]
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Australia
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Date submitted for ethics approval [8]
243756
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Approval date [8]
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07/12/2006
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Ethics approval number [8]
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EC00332
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Summary
Brief summary
The long-term presence of physical and psychosocial symptoms following breast cancer treatment is well established. However, Queensland is a geographically dispersed state, where many women with breast cancer live in rural and remote areas with limited support resources. Queensland-based research highlights that these women are more likely to have more extensive surgeries, and experience poorer quality of life and higher unmet needs. Exercise is one strategy with a large evidence base supporting its effectiveness in reducing symptoms and improving quality of life (QoL) among women following breast cancer. However, the majority of studies have been conducted overseas, and with women in urban areas. This pilot study will evaluate the feasibility of a telephone-delivered exercise-based rehabilitation support program for women newly diagnosed with breast cancer living in regional, rural and remote areas of Queensland, Australia. Feasibility and effect size data from the pilot study will be used to refine the intervention and to inform a subsequent application for a fully powered randomized controlled trial. This study forms an arm of a larger study that is currently being undertaken (ACTRN12606000233527) with an urban sample of women who have received breast cancer treatment via Brisbane-based hospitals (Royal Brisbane & Women’s Hospital, Mater Hospital and Wesley Hospital).
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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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Elizabeth Eakin
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Address
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Cancer Prevention Research Centre, School of Population Health, Level 3 Public Health Building, The University of Queensland, Herston Road Herston QLD 4006
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Country
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Australia
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Phone
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+61 7 3346 4692
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Fax
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+61 7 3365 5540
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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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Elizabeth Eakin
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Address
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Cancer Prevention Research Centre, School of Population Health, Level 3 Public Health Building, The University of Queensland, Herston Road Herston QLD 4006
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Country
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Australia
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Phone
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+61 7 3346 4692
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Fax
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+61 7 3365 5540
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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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