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Trial registered on ANZCTR
Registration number
ACTRN12606000511538
Ethics application status
Not yet submitted
Date submitted
7/12/2006
Date registered
8/12/2006
Date last updated
8/12/2006
Type of registration
Prospectively registered
Titles & IDs
Public title
Stroke incontinence study
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Scientific title
A randomised controlled trial to evaluate the effects of a continence promotion program including real time ultrasound as biofeedback for pelvic floor muscle rehabilitation, delivered to stroke survivors to reduce urinary incontinence and lower urinary tract symptoms.
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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:
Urinary incontinence after stroke
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Condition category
Condition code
Stroke
1583
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Renal and Urogenital
1584
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0
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Other renal and urogenital disorders
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Physical Medicine / Rehabilitation
1585
1585
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0
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Other physical medicine / rehabilitation
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Intervention Group will receive daily physiotherapy stroke rehabilitation. As well as this, they will receive specifically designed:
Continence promotion intervention that will be tailored to patient's requirements and might include:
Bladder training,
Pelvic floor muscle exercises,
Real Time Ultrasound Biofeedback for pelvic floor and transversus abdominis muscles.
Pelvic floor muscle exercises will be encouraged at each physiotherapy intervention. Bladder training protocols will need to be repeated daily since stroke patients often have problems with short term memory deficits.
Real time ultrasound provides images of muscles as they actually contract. Biofeedback using real time ultrasound will be used to teach patients how to contract pelvic floor muscles and abdominal muscles. It will be used daily until patients are aware of the muscle contraction and no longer require biofeedback. This will differ between patients
Information booklet based on succesfully developed continence promotion booklets previously produced by Dr Chiarelli aimed at different clinical groups e.g postpartum women, older people following surgery for fractured hip.
The "Waterworks after Stroke" information booklet will be designed using health promotion principles and with the assistance of speech pathologists who have special expertise in management of stroke patients. Booklet will be given to patients and their carers. Acceptability, understandability and relevance of the contents of the booklet will be tested in both patient and carer groups
Intervention progressed as required for the duration of patient's stay in Rehabiliation Unit
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Intervention code [1]
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Rehabilitation
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Comparator / control treatment
Control group to receive usual care consisting of routine physiotherapy post stroke rehabiliation tailored to individual patient needs.
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Control group
Active
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Outcomes
Primary outcome [1]
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Urinary incontinence, will be measured using:
24 hour pad test
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Assessment method [1]
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Timepoint [1]
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On admission to the rehabilitation unit and immediately prior to discharge
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Primary outcome [2]
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Urinary incontinence, will be measured using:
Validated questionnaire
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Assessment method [2]
2188
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Timepoint [2]
2188
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On admission to the rehabilitation unit and immediately prior to discharge
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Primary outcome [3]
2189
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Urinary incontinence, will be measured using :
Ultrasound assessment of pelvic floor and abdominal muscle function.
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Assessment method [3]
2189
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Timepoint [3]
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On admission to the rehabilitation unit and immediately prior to discharge
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Secondary outcome [1]
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Functional Independence measure
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Assessment method [1]
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Timepoint [1]
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Time points on admission to unit and immediately prior to discharge
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Secondary outcome [2]
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Trunk control test.
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Assessment method [2]
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Timepoint [2]
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Time points on admission to unit and immediately prior to discharge
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Eligibility
Key inclusion criteria
Admitted to stroke rehabilitation unit.
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Minimum age
No limit
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Maximum age
No limit
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Unaware of loss of bladder controlIndwelling urethral catheter in situdocumentation of pelvic organ prolapse, suffering chronic obstructive pulmonary disease, psychological problems, other neurological conditions, not understanding English, severely hearing impaired, severely sight impaired.
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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)
central randomisation by phone.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computer generated randomisation
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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
Assessors at final assessment at time of discharge from the unit will be blinded to patient's group allocation
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Phase
Phase 4
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
27/02/2007
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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
50
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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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University
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Name [1]
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University of Newcastle Faculty of Health
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Address [1]
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Country [1]
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Australia
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Primary sponsor type
Individual
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Name
Dr Pauline Chiarelli
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Address
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Country
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Secondary sponsor category [1]
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University
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Name [1]
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Centre for Research in Gender Health and Aging
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Address [1]
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Country [1]
1524
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Ethics approval
Ethics application status
Not yet submitted
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Ethics committee name [1]
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Rankin Park Hospital Stroke Rehabilitation Unit
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Ethics committee address [1]
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
3195
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Approval date [1]
3195
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Ethics approval number [1]
3195
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Ethics committee name [2]
3196
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Belmont District Hospital Stroke Rehabilitation Unit
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Ethics committee address [2]
3196
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Ethics committee country [2]
3196
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Australia
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Date submitted for ethics approval [2]
3196
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Approval date [2]
3196
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Ethics approval number [2]
3196
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Ethics committee name [3]
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Maitland Hospital Stroke Rehabilitation Unit
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Ethics committee address [3]
3197
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Ethics committee country [3]
3197
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Australia
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Date submitted for ethics approval [3]
3197
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Approval date [3]
3197
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Ethics approval number [3]
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Summary
Brief summary
A specifically designed continence promotion program including real time ultrasound as biofeedback for pelvic floor muscle rehabilitation, delivered to stroke survivors in stroke rehabilitation units will reduce urinary incontinence and lower urinary tract symptoms in stroke survivors
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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 Pauline Chiarelli
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Address
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Box 24 Hunter Building, University of Newcastle, Callaghan 2308 NSW
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Country
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Australia
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Phone
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61 2 49216046
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Fax
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61 2 497902
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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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Professor Julie Byles
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Address
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Director, Research Centre for Gender, Health and Ageing
Level 2, David Madison Sciences Block
Cnr King and Watt Sts
Newcastle NSW 2300
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Country
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Australia
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Phone
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61 2 4923 6643
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Fax
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61 2 492 36321
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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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