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Trial registered on ANZCTR
Registration number
ACTRN12605000490673
Ethics application status
Approved
Date submitted
12/09/2005
Date registered
23/09/2005
Date last updated
20/06/2016
Type of registration
Retrospectively registered
Titles & IDs
Public title
Women's Lifestyle Study
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Scientific title
Women in action: a randomised controlled trial to evaluate the effects of a physical activity intervention on risk factors for diabetes and heart disease in 40-75yr old women
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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:
Risk factors associated with type 2 diabetes and heart disease
612
0
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Condition category
Condition code
Metabolic and Endocrine
684
684
0
0
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Diabetes
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Cardiovascular
685
685
0
0
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Coronary heart disease
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Intervention: Baseline measures followed by physical activity advice given by telephone over 5mths, a face-to-face visit with a research nurse at 6mths and further telephone contact at 9mths. Intervention complete at 9mths, outcomes assessed at 12 and 24mths.
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Intervention code [1]
480
0
Prevention
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Comparator / control treatment
Control: Baseline measures followed by reassessment at 12 and 24mths.
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Control group
Placebo
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Outcomes
Primary outcome [1]
835
0
Adherence to physical activity
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Assessment method [1]
835
0
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Timepoint [1]
835
0
At 12 and 24 months
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Primary outcome [2]
836
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Cost-effectiveness ratios
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Assessment method [2]
836
0
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Timepoint [2]
836
0
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Secondary outcome [1]
1647
0
Blood pressure
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Assessment method [1]
1647
0
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Timepoint [1]
1647
0
Measured at baseline and repeated at 12 and 24 months.
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Secondary outcome [2]
1648
0
Waist circumference
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Assessment method [2]
1648
0
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Timepoint [2]
1648
0
Measured at baseline and repeated at 12 and 24 months.
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Secondary outcome [3]
1649
0
Weight
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Assessment method [3]
1649
0
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Timepoint [3]
1649
0
Measured at baseline and repeated at 12 and 24 months.
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Secondary outcome [4]
1650
0
Fasting bloods including glucose
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Assessment method [4]
1650
0
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Timepoint [4]
1650
0
Measured at baseline and repeated at 12 and 24 months.
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Secondary outcome [5]
1651
0
Lipids
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Assessment method [5]
1651
0
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Timepoint [5]
1651
0
Measured at baseline and repeated at 12 and 24 months.
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Secondary outcome [6]
1652
0
HBA1c and insulin
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Assessment method [6]
1652
0
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Timepoint [6]
1652
0
Measured at baseline and repeated at 12 and 24 months.
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Secondary outcome [7]
1653
0
Physical fitness
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Assessment method [7]
1653
0
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Timepoint [7]
1653
0
Measured at baseline and repeated at 12 and 24 months.
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Eligibility
Key inclusion criteria
Able to participate in moderate intensity physical activity.
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Minimum age
40
Years
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Maximum age
75
Years
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Blood pressure >=200/110; deemed ineligible for participation in moderate intensity physical activity by GP (e.g. acutely unwell or injured).
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Study design
Purpose of the study
Prevention
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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)
Sealed envelope containing group allocation opened by studynurse at completion of baseline measures.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computer generated by independent researcher using STATA in random blocks with variable block sizes
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
24/11/2004
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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
1080
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
206
0
New Zealand
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State/province [1]
206
0
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Funding & Sponsors
Funding source category [1]
759
0
Charities/Societies/Foundations
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Name [1]
759
0
National Heart Foundation of NZ
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Address [1]
759
0
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Country [1]
759
0
New Zealand
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Funding source category [2]
760
0
Government body
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Name [2]
760
0
Hutt Valley District Health Board
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Address [2]
760
0
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Country [2]
760
0
New Zealand
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Funding source category [3]
761
0
Government body
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Name [3]
761
0
Lottery Health Research Grants Board
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Address [3]
761
0
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Country [3]
761
0
New Zealand
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Primary sponsor type
Commercial sector/Industry
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Name
National Heart Foundation of NZ
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Address
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Country
New Zealand
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Secondary sponsor category [1]
627
0
Government body
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Name [1]
627
0
Hutt Valley District Health Board
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Address [1]
627
0
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Country [1]
627
0
New Zealand
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Secondary sponsor category [2]
628
0
Government body
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Name [2]
628
0
Lottery Health Research Grants Board
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Address [2]
628
0
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Country [2]
628
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
2006
0
the Wellington Ethics Committee (now known as the Central Regional Ethics Committee)
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Ethics committee address [1]
2006
0
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Ethics committee country [1]
2006
0
New Zealand
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Date submitted for ethics approval [1]
2006
0
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Approval date [1]
2006
0
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Ethics approval number [1]
2006
0
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Summary
Brief summary
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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
36398
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Address
36398
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Country
36398
0
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Phone
36398
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Fax
36398
0
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Email
36398
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Contact person for public queries
Name
9669
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Dr Sally Rose
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Address
9669
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Department of Primary Health Care and General Practice
Wellington School of Medicine & Health Sciences
University of Otago
PO Box 7343
Wellington
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Country
9669
0
New Zealand
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Phone
9669
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+64 4 9186249
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Fax
9669
0
+64 4 3855473
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Email
9669
0
[email protected]
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Contact person for scientific queries
Name
597
0
Dr Beverley Lawton
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Address
597
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Department of Primary Health Care and General Practice
Wellington School of Medicine & Health Sciences
University of Otago
PO Box 7343
Wellington
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Country
597
0
New Zealand
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Phone
597
0
+64 4 3855995 ext. 4893
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Fax
597
0
+64 4 3855473
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Email
597
0
[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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