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Trial registered on ANZCTR
Registration number
ACTRN12611000797976
Ethics application status
Approved
Date submitted
26/07/2011
Date registered
29/07/2011
Date last updated
7/10/2015
Type of registration
Prospectively registered
Titles & IDs
Public title
Can patients reproduce partial weight bearing orders?
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Scientific title
Partial weight bearing in orthopaedic in-patients: ability to reproduce partial weight bearing orders, factors influencing this and effect on clinical outcomes.
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Secondary ID [1]
262699
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Nil.
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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:
Orthopaedic inpatients who are prescribed partial weight bearing as part of their management
270403
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Condition category
Condition code
Musculoskeletal
270545
270545
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0
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Other muscular and skeletal disorders
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Intervention/exposure
Study type
Observational
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
All participants will receive standard medical, nursing and allied health care during and after their hospital admission. This care, including instruction in partial weight bearing during mobilisation by physiotherapists, will not change as a result of participation in the current study. Our physiotherapists currently use the hand-under-foot or bathroom scale method to instruct patients in partial weight bearing, with the method chosen at the discretion of the treating physiotherapist. Instruction is repeated until the patient and physiotherapist are confident that the patient can reproduce the partial weight bearing orders. Further instruction on subsequent episodes of mobilisation is undertaken as deemed necessary. Additionally, when mobilising patients, physiotherapy staff observe the patient’s style of mobilisation and estimate whether partial weight bearing to the prescribed level is occurring. Repeated instruction is provided for patients when over-loading is suspected.
Instruction in partial weight bearing status will occur only during the period of hospitalisation.
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Intervention code [1]
267047
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Not applicable
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Comparator / control treatment
Uncontrolled
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
269290
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Maximum difference between the target load and actual load will be recorded (in kg) using the SmartStep monitor.
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Assessment method [1]
269290
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Timepoint [1]
269290
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Daily weekday basis during the period of hospitalisation.
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Primary outcome [2]
269291
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Mean (standard deviation) weight during the period of mobilisation will also be recorded using the SmartStep monitor.
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Assessment method [2]
269291
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Timepoint [2]
269291
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Daily weekday basis during the period of hospitalisation.
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Secondary outcome [1]
279312
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In order to investigate factors that could potentially impact on patients' ability to reproduce partial weight bearing orders, descriptive data will be collected. These data will include age, sex, body mass index, primary diagnosis, medical conditions that could affect patients' ability to perform partial weight bearing (eg, musculoskeletal or neurological conditions), conditions that could affect patients' ability to understand partial weight bearing instructions (eg, English as a second language, cognitive impairment) and pain at the time of mobilisation (measured on a verbal analogue scale where 0 = no pain and 10 = worst pain imaginable). These data will collected by one of the investigators (SK, TM or CJ) from medical records or by questioning the patient.
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Assessment method [1]
279312
0
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Timepoint [1]
279312
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Daily weekday basis during the period of hospitalisation.
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Secondary outcome [2]
279313
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Broad clinical outcomes will be retrieved from data routinely recorded on a form which is completed by orthopaedic surgeons/registrars when patients attend Orthopaedic Outpatient clinics. This form includes information about patients' ability to walk, pain, range of motion, complications and xray findings. Importantly, the latter two points (ie, complications and xray findings) will indicate whether there has been a clinically important loss of fracture reduction and/or implant loosening, which would be the most important adverse effects that might result from excessive weight bearing during the period of fracture healing and/or recovery from orthopaedic surgery.
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Assessment method [2]
279313
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Timepoint [2]
279313
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Three months post-injury.
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Eligibility
Key inclusion criteria
Adult patients admitted to the Royal Adelaide Hospital with an orthopaedic problem/condition where the management includes the prescription of partial weight bearing.
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Minimum age
18
Years
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Maximum age
No limit
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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
Unwilling to participate
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Study design
Purpose
Natural history
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Duration
Longitudinal
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Selection
Convenience sample
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Timing
Prospective
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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
1/09/2011
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Actual
22/02/2012
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Date of last participant enrolment
Anticipated
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Actual
19/03/2012
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
47
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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]
267519
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Hospital
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Name [1]
267519
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Royal Adelaide Hospital Allied Health Research Grant
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Address [1]
267519
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Royal Adelaide Hospital
North Terrace
Adelaide
South Australia 5000
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Country [1]
267519
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Australia
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Primary sponsor type
Hospital
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Name
Royal Adelaide Hospital
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Address
North Terrace
Adelaide
South Australia 5000
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Country
Australia
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Secondary sponsor category [1]
266561
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None
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Name [1]
266561
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Address [1]
266561
0
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Country [1]
266561
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
269485
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Royal Adelaide Hospital Research Ethics Committee
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Ethics committee address [1]
269485
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Research Ethics Committee Level 3, Hanson Institute Royal Adelaide Hospital North Terrace Adelaide South Australia 5000
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Ethics committee country [1]
269485
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Australia
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Date submitted for ethics approval [1]
269485
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26/07/2011
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Approval date [1]
269485
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26/07/2011
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Ethics approval number [1]
269485
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110711
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Summary
Brief summary
The main purpose of this study is to determine objectively whether orthopaedic in-patients are able to reproduce partial weight bearing orders by assessing dynamic weight bearing using a highly accurate insole monitor. The study also seeks to investigate factors that influence patients’ ability to accurately reproduce partial weight bearing orders. Finally, the study will investigate, in a preliminary manner, whether the ability to accurately reproduce partial weight bearing orders affects clinical outcomes.
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Trial website
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Trial related presentations / publications
Publication: Yu S, McDonald T, Jesudason C, Stiller K, Sullivan T (2014) Orthopedic in-patients’ ability to accurately reproduce partial weight bearing orders. Orthopedics 37:e10-e18. Presentation: October 2013; Yu S, McDonald T, Jesudason C, Stiller K, Sullivan T (2013) Orthopaedic in-patients’ ability to reproduce partial weight bearing orders: factors influencing this and effect on clinical outcomes. An observational study. Australian Physiotherapy Association Physiotherapy Conference, Melbourne, Australia.
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Public notes
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Contacts
Principal investigator
Name
32923
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Dr Kathy Stiller
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Address
32923
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Physiotherapy Department Royal Adelaide Hospital North Terrace Adelaide South Australia 5000
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Country
32923
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Australia
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Phone
32923
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61 8 82225334
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Fax
32923
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61 8 82224279
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Email
32923
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[email protected]
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Contact person for public queries
Name
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Kathy Stiller
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Address
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Physiotherapy Department
Royal Adelaide Hospital
North Terrace
Adelaide
South Australia 5000
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Country
16170
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Australia
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Phone
16170
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61 8 82225334
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Fax
16170
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61 8 82224279
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Email
16170
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[email protected]
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Contact person for scientific queries
Name
7098
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Kathy Stiller
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Address
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Physiotherapy Department
Royal Adelaide Hospital
North Terrace
Adelaide
South Australia 5000
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Country
7098
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Australia
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Phone
7098
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61 8 82225334
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Fax
7098
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61 8 82224279
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Email
7098
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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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