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Trial registered on ANZCTR
Registration number
ACTRN12609000536268
Ethics application status
Approved
Date submitted
28/06/2009
Date registered
3/07/2009
Date last updated
6/07/2012
Type of registration
Prospectively registered
Titles & IDs
Public title
Efficacy of Clinical Pilates versus general exercise for chronic low back pain: a randomised controlled trial.
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Scientific title
Effect on low back function of Clinical Pilates versus general exercise in adults with chronic low back pain
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Secondary ID [1]
252114
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Effect on chronic low back pain and function of Clinical Pilates
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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 low back pain
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Condition category
Condition code
Musculoskeletal
237435
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0
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Other muscular and skeletal disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
People with chronic low back pain will be screened via telephone and undergo a physical screening. Baseline testing will be performed at The University of Melbourne and the participant randomised into one of two groups (i) Clinical Pilates (ii) General Exercise. the intervention will last for 6 weeks after which all participants will be reassessed by the same blinded assessor. Both interventions will comprise 12X1 hour visits for supervised exercise over 6 weeks (2 per week) to the trial clinic plus home exercises daily. The supervised sessions will be conducted by a physiotherapist in small group format with up to four participants. An exercise diary will be kept and monitored by the supervising physiotherapist. The Clinical Pilates programs are tailor-made Pilates exercises based on a history and physical assessment. The exercises are chosen according to findings on assessment and are performed on pilates equipment, with home exercises prescribed as an adjunct to the equipment-based exercises.
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Intervention code [1]
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Treatment: Other
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Comparator / control treatment
The general exercise program is a standardised set of exercises including exercise bike, abdominal, back and limb strengthening using weights, exercise ball and theraband tubing.
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Control group
Active
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Outcomes
Primary outcome [1]
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Quebec Low back Pain questionnaire
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Assessment method [1]
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Timepoint [1]
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Baseline and 6 weeks following randomisation, with follow up at 3 months and 6 months following completion of (6 week) program
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Secondary outcome [1]
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Low Back pain with a Visual Analogue Scale (VAS)
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Assessment method [1]
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Timepoint [1]
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Baseline and 6 weeks following randomisation, with follow up at 3 months and 6 months following completion of (6 week) program
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Secondary outcome [2]
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Function with a Patient Specific Functional Scale (PSFS)
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Assessment method [2]
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Timepoint [2]
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Baseline and 6 weeks following randomisation, with follow up at 3 months and 6 months following completion of (6 week) program
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Secondary outcome [3]
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Quality of Life with a 36-Item Short-Form Health Survey (SF 36)
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Assessment method [3]
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Timepoint [3]
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Baseline and 6 weeks following randomisation, with follow up at 3 months and 6 months following completion of (6 week) program
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Secondary outcome [4]
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Self Efficacy with a Pain Self Efficacy Questionnaire
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Assessment method [4]
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Timepoint [4]
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Baseline and 6 weeks following randomisation, with follow up at 3 months and 6 months following completion of (6 week) program
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Secondary outcome [5]
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Saggital Spinal Posture and Range of Motion with a Digital Dual Inclinometer
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Assessment method [5]
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Timepoint [5]
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Baseline and 6 weeks following randomisation
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Eligibility
Key inclusion criteria
Low back pain with or without leg pain on most days for the last three months, pain greater than 4/10,
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Minimum age
18
Years
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Maximum age
70
Years
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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
Back Surgery, Spinal Infection, Fractures , Osteoporosis, Hip Osteoarthritis, Ankylosing Spondylitis, Rheumatoid Arthritis, Low back pain of non-musculoskeletal origin, Workcover, Transport Accident Commission or legal claim, Pregnancy, Acute disc prolapse, treatment involving exercise in the last six months
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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)
After screening procedures, eligible volunteers allocated to a group at random. Sealed opaque envelopes kept in central location and opened after baseline testing by administrator
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Block randomisation , computer generated random number list. Variable block sizes will be used , stratified for age.
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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
Independent blinded assessor
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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
Active, not recruiting
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Date of first participant enrolment
Anticipated
21/07/2009
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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
86
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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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Commercial sector/Industry
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Name [1]
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DMA Clinical Pilates
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Address [1]
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1 Yarra Street South Yarra Victoria 3141
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Country [1]
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Australia
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Primary sponsor type
Individual
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Name
Henry Wajswelner
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Address
Centre for Health Exercise and Sports Medicine, Melbourne Physiotherapy School, The University of Melbourne 200 Berkeley Street Carlton VIC 3053
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Country
Australia
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Secondary sponsor category [1]
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Individual
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Name [1]
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Professor Kim Bennell
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Address [1]
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Centre for Health Exercise and Sports Medicine, Melbourne Physiotherapy School, The University of Melbourne 200 Berkeley Street Carlton VIC 3053
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Country [1]
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Australia
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Other collaborator category [1]
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Individual
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Name [1]
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Mr Tim Wrigley
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Address [1]
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Centre for Health Exercise and Sports Medicine, Melbourne Physiotherapy School, The University of Melbourne 200 Berkeley Street Carlton VIC 3053
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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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The University of Melbourne Human Research Ethics Committee
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Ethics committee address [1]
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Melbourne Research Office The University of Melbourne Level 5, Alan Gilbert Building VIC 3010
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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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16/06/2009
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Approval date [1]
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24/06/2009
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Ethics approval number [1]
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0931800
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Summary
Brief summary
In people with chronic low back pain, a randomised controlled trial comparing the effect of a six week clinical pilates program with a general exercise program on back function with a 3 and 6 month follow up.
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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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Henry Wajswelner
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Address
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617 Canning street North Carlton VIC 3054
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Country
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Australia
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Phone
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+61 3 93889387
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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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Henry Wajswelner
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Address
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617 Canning street North Carlton VIC 3054
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Country
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Australia
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Phone
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+61 428292265
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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
Source
Title
Year of Publication
DOI
Embase
Exercise therapy for chronic low back pain.
2021
https://dx.doi.org/10.1002/14651858.CD009790.pub2
N.B. These documents automatically identified may not have been verified by the study sponsor.
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