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Trial registered on ANZCTR
Registration number
ACTRN12606000284561
Ethics application status
Not yet submitted
Date submitted
4/07/2006
Date registered
5/07/2006
Date last updated
5/07/2006
Type of registration
Retrospectively registered
Titles & IDs
Public title
A Lifestyle Intervention Program to treat Mild to Moderate Obstructive Sleep apnoea
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Scientific title
A Diet and Exercise Program to Improve Sleep-Disordered Breathing, lose weight and improve fitness in patients with Obstructive Sleep Apnoea
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Universal Trial Number (UTN)
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Trial acronym
nil
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Obstructive Sleep Apnoea
1259
0
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Condition category
Condition code
Respiratory
1345
1345
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0
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Sleep apnoea
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
The following interventions are implemented together for 4 months:
1. Diet - using very low energy liquid meal replacement (Optifast) in combination with low fat and low carbohydrate meals.
2. Exercise - both aerobic using exercise bikes and resistance using weights in a hospital gym, as well as at home. The hospital based sessions are for 40 minutes to 1 hour, 3 times each week for 8 weeks then once each week for 8 weeks. In addition, subjects are asked to exercise at home for 30-60 minutes on the days that they do not attend the hospital gym.
There are no drugs involved.
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Intervention code [1]
874
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Lifestyle
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Comparator / control treatment
No comparator.
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Apnoea Hypopnoea Index
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Assessment method [1]
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Timepoint [1]
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Measured at the end of the 4 month treatment period.
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Secondary outcome [1]
3214
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Weight Loss
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Assessment method [1]
3214
0
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Timepoint [1]
3214
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Measured at the end of the 4 month treatment period.
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Secondary outcome [2]
3215
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Fitness
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Assessment method [2]
3215
0
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Timepoint [2]
3215
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Measured at the end of the 4 month treatment period.
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Secondary outcome [3]
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Blood Pressure
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Assessment method [3]
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Timepoint [3]
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Measured at the end of the 4 month treatment period.
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Secondary outcome [4]
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Daytime Function
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Assessment method [4]
3217
0
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Timepoint [4]
3217
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Measured at the end of the 4 month treatment period.
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Eligibility
Key inclusion criteria
AHI at least 10waist circumference at least 95cm in females, 100cm in males.
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Minimum age
18
Years
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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
Physical or psychological co-morbiditiesInability to exerciseDietary restrictionsInsulin requiring diabetesRenal or liver disease.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
N/A
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not 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
Stopped early
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Data analysis
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Reason for early stopping/withdrawal
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Date of first participant enrolment
Anticipated
1/04/2006
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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
10
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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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Funding & Sponsors
Funding source category [1]
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Other
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Name [1]
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Institute for Breathing and Sleep
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Address [1]
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Country [1]
1472
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Australia
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Primary sponsor type
Other
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Name
Institute for Breathing and Sleep
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Address
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Country
Australia
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Secondary sponsor category [1]
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Charities/Societies/Foundations
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Name [1]
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Physiotherapy Research Foundation
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Address [1]
1299
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Country [1]
1299
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Australia
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Ethics approval
Ethics application status
Not yet submitted
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Ethics committee name [1]
2854
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Austin Health Human Research Ethics Committee
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Ethics committee address [1]
2854
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Ethics committee country [1]
2854
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Australia
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Date submitted for ethics approval [1]
2854
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Approval date [1]
2854
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Ethics approval number [1]
2854
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Summary
Brief summary
Subjects with mild to moderate obstructive sleep apnoea will be invited to participate in a supervised 4-month diet and exercise program. We will measure daytime function, quality of life and severity of sleep-disordered breathing before and after the study, and in addition will followup subjects for 12 months after they complete the active intervention protocol.
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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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Dr Maree Barnes
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Address
10063
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Institute for Breathing and Sleep
Austin Health
Studley Road
Heidelberg
VIC
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Country
10063
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Australia
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Phone
10063
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61 3 9496 5756
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Fax
10063
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61 3 9496 5124
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Email
10063
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[email protected]
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Contact person for scientific queries
Name
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Dr Maree Barnes
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Address
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Institute for Breathing and Sleep
Austin Health
Studley Road
Heidelberg
Victoria
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Country
991
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Australia
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Phone
991
0
61 3 9496 5756
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Fax
991
0
61 3 9496 5124
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Email
991
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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