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Trial registered on ANZCTR
Registration number
ACTRN12614000631606
Ethics application status
Approved
Date submitted
29/05/2014
Date registered
13/06/2014
Date last updated
23/01/2017
Type of registration
Retrospectively registered
Titles & IDs
Public title
Cognition and Bimanual Performance in Children with Unilateral Cerebral Palsy
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Scientific title
Cognition and Bimanual Performance in Children with Unilateral Cerebral Palsy
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Secondary ID [1]
284701
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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:
Cerebral palsy
292054
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Condition category
Condition code
Neurological
292390
292390
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0
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Other neurological disorders
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Intervention/exposure
Study type
Observational
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Patient registry
False
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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
Not applicable: Observational study. Eligible children will be assessed on a single occasion using a range of outcome measures relating to upper limb bimanual performance, motor planning, neuropsychological function and static magnetic resonance imaging (MRI).
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Intervention code [1]
289489
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Not applicable
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Assisting Hand Assessment - Bimanual upper limb performance
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Assessment method [1]
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Timepoint [1]
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Single occasion only. Cross sectional study
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Primary outcome [2]
292254
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Box and Blocks Test - Unilateral upper limb speed and dexterity
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Assessment method [2]
292254
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Timepoint [2]
292254
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Single occasion only. Cross sectional study
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Primary outcome [3]
292255
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ABILHAND-Kids - Manual ability
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Assessment method [3]
292255
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Timepoint [3]
292255
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Single occasion only. Cross sectional study
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Secondary outcome [1]
308554
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The “Sword Test” - Anticipatory motor planning
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Assessment method [1]
308554
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Timepoint [1]
308554
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Single occasion only. Cross sectional study
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Secondary outcome [2]
308555
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Wechsler Intelligence Scale for Children (4th Ed) - Intelligence
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Assessment method [2]
308555
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Timepoint [2]
308555
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Single occasion only. Cross sectional study
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Secondary outcome [3]
308556
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NEPSY-II - Executive function and attention, language, memory and learning, sensorimotor, visuospatial processing, social perception
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Assessment method [3]
308556
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Timepoint [3]
308556
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Single occasion only. Cross sectional study
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Secondary outcome [4]
308557
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Test of Everyday Attention for Children (TEA-Ch) - Attention
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Assessment method [4]
308557
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Timepoint [4]
308557
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Single occasion only. Cross sectional study
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Secondary outcome [5]
308558
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Tower of London - Executive functioning
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Assessment method [5]
308558
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Timepoint [5]
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Single occasion only. Cross sectional study
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Secondary outcome [6]
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Sky Search DT - Sustained-divided attention
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Assessment method [6]
308559
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Timepoint [6]
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Single occasion only. Cross sectional study
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Secondary outcome [7]
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Conners 3rd Edition - Everyday executive abilities
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Assessment method [7]
308560
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Timepoint [7]
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Single occasion only. Cross sectional study
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Secondary outcome [8]
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The Behaviour Rating Inventory of Executive Function (BRIEF) – Parent Version - Parent ratings of current functional, emotional and behavioural manifestations of executive dysfunction.
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Assessment method [8]
308561
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Timepoint [8]
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Single occasion only. Cross sectional study
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Secondary outcome [9]
308562
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Automated Working Memory Assessment (AWMA) - Visuospatial working memory
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Assessment method [9]
308562
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Timepoint [9]
308562
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Single occasion only. Cross sectional study
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Secondary outcome [10]
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Static Magnetic Resonance Imaging - Type and severity of brain injury
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Assessment method [10]
308734
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Timepoint [10]
308734
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Single occasion only. Cross sectional study
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Eligibility
Key inclusion criteria
1. Diagnosis of congenital unilateral cerebral palsy as diagnosed and reported in the medical history by a medical specialist (i.e. neurologist, paediatrician);
2. Age 6 to 12 years at the time of recruitment.
3. Sufficient cooperation to complete the assessments (ie. Ascent).
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Minimum age
6
Years
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Maximum age
12
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
1. Upper limb surgery within 12 months of assessment.
2. Injection of Botulinum toxin-A within 3 months of assessment.
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Study design
Purpose
Natural history
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Duration
Cross-sectional
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Selection
Defined population
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Timing
Prospective
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Statistical methods / analysis
A sample size of 150 is sufficient to detect a minimum effect size of 0.12 (Cohen’s f2) with 10 predictors at 80% power and a probability level of 0.05.
Sample characteristics, including full cognitive functioning, motor functioning, demographic and data will be explored using descriptive data analysis. Descriptive data analyses will be completed by examining distributions and measures of the middle and spread in continuously scaled variables and by constructing frequency distributions for categorical variables.
Descriptive data analyses will be used to explore the data, and will be completed by examining distributions and measures of the middle and spread in continuously scaled variables and by constructing frequency distributions for categorical variables.
The primary hypothesis (a relationship exists among how well children with unilateral CP use their two hands together and aspects of their cognition function such as attention, goal setting, information processing and everyday executive abilities) will be assessed in two ways. To assess the association between and among bimanual upper limb motor performance (Assisting Hand Assessment) and measures of cognition, we will produce scatter plots and calculate correlation coefficients. We will examine the association between bimanual upper limb performance and cognition variable using univariable linear regression. Variables where there is a significant association with bimanual upper limb performance (p=0.1) will then be retained to be entered into a multivariable regression analysis adjusting for variables such as sex and age and others that could confound associations between bimanual upper limb performance and cognition.
Our second hypothesis (the relationship among cognition and bimanual hand function is influenced by underlying brain pathology) will be evaluated using logistic regression analysis because the outcome measurement is dichotomous (MRI lesion characteristics – as per protocol). We will examine the association between neuropathology (MRI), bimanual upper limb performance and cognitive variables. Variables where there is a significant association with neuropathology and bimanual upper limb performance (p=0.1) and neuropathology and cognitive variables (p=0.1) will be retained to be entered into a multivariable regression analysis adjusting for variables such as sex and age and other variables that could confound associations between the dependent variable and covariate.
All statistical analyses will be conducted on Stata V12.1 and led by a biostatistician with input from the clinical and research team.
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/01/2013
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Actual
25/01/2013
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Date of last participant enrolment
Anticipated
31/12/2014
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Actual
14/08/2015
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Date of last data collection
Anticipated
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Actual
24/08/2015
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Sample size
Target
150
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Accrual to date
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Final
131
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Recruitment in Australia
Recruitment state(s)
NSW,QLD,WA,VIC
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Recruitment hospital [1]
2520
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Monash Medical Centre - Clayton campus - Clayton
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Recruitment hospital [2]
2521
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Royal Children's Hospital - Herston
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Recruitment hospital [3]
2523
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The Royal Childrens Hospital - Parkville
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Recruitment hospital [4]
2524
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Princess Margaret Hospital - Subiaco
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Funding & Sponsors
Funding source category [1]
289323
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Charities/Societies/Foundations
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Name [1]
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Cerebral Palsy International Research Foundation
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Address [1]
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186 Princeton Hightstown Road; Building 4, 2nd Floor
Princeton Junction, NJ 08550
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Country [1]
289323
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United States of America
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Funding source category [2]
295409
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Charities/Societies/Foundations
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Name [2]
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Cerebral Palsy Alliance
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Address [2]
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187 Allambie Road, Allambie Heights, NSW 2100
PO Box 6427, Frenchs Forest NSW 2086
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Country [2]
295409
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Australia
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Primary sponsor type
Hospital
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Name
Monash Children's Hospital
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Address
246 Clayton Rd, Clayton, Victoria, 3168
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Country
Australia
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Secondary sponsor category [1]
287992
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None
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Name [1]
287992
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Address [1]
287992
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Country [1]
287992
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
291084
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Monash Health
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Ethics committee address [1]
291084
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Research Directorate Monash Health Monash Medical Centre 246 Clayton Road Clayton Victoria 3168
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Ethics committee country [1]
291084
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Australia
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Date submitted for ethics approval [1]
291084
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21/06/2012
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Approval date [1]
291084
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05/09/2012
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Ethics approval number [1]
291084
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12167B
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Ethics committee name [2]
291085
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Royal Children's Hospital, Melbourne
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Ethics committee address [2]
291085
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50 Flemington Rd Parkville, Victoria, 3052
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Ethics committee country [2]
291085
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Australia
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Date submitted for ethics approval [2]
291085
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01/11/2012
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Approval date [2]
291085
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16/11/2012
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Ethics approval number [2]
291085
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32232 A
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Ethics committee name [3]
291086
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Royal Children's Hospital, Queensland
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Ethics committee address [3]
291086
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Level 3, RCH Foundation Building Royal Children’s Hospital Herston QLD 4029
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Ethics committee country [3]
291086
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Australia
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Date submitted for ethics approval [3]
291086
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03/12/2012
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Approval date [3]
291086
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17/12/2012
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Ethics approval number [3]
291086
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HREC/121QRCHl218
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Ethics committee name [4]
291087
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Cerebral Palsy Alliance
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Ethics committee address [4]
291087
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187 Allambie Rd, Allambie Heights, NSW, 2100
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Ethics committee country [4]
291087
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Australia
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Date submitted for ethics approval [4]
291087
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03/12/2012
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Approval date [4]
291087
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30/12/2012
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Ethics approval number [4]
291087
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2012-12-03
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Ethics committee name [5]
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Princess Margaret Hospital for Children
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Ethics committee address [5]
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Roberts Road Subiaco, Western Australia, 6008
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Ethics committee country [5]
291149
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Australia
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Date submitted for ethics approval [5]
291149
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06/05/2013
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Approval date [5]
291149
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03/09/2013
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Ethics approval number [5]
291149
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2013062EP
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Summary
Brief summary
This project is a cross-sectional observational study examining the association between and among cognition, type and severity of brain injury and upper limb bimanual performance in a large sample of children (n=150), aged 6 to 12 years, with unilateral CP. The project will be conducted across 5 Australian sites specializing in the management of children with CP. The aim of this Project is to: (a) describe the association between and among cognition and upper limb bimanual performance in children with unilateral CP; (b) describe the association between and among cognition and upper limb bimanual performance and type and severity of brain injury in children with unilateral CP.
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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
48838
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Dr Brian Hoare
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Address
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Monash Children's Hospital
246 Clayton Rd
Clayton, Victoria, 3168
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Country
48838
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Australia
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Phone
48838
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+61395944620
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Fax
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Email
48838
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[email protected]
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Contact person for public queries
Name
48839
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Brian Hoare
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Address
48839
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Monash Children's Hospital
246 Clayton Rd
Clayton, Victoria, 3168
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Country
48839
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Australia
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Phone
48839
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+61395944620
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Fax
48839
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Email
48839
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[email protected]
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Contact person for scientific queries
Name
48840
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Brian Hoare
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Address
48840
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Monash Children's Hospital
246 Clayton Rd
Clayton, Victoria, 3168
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Country
48840
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Australia
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Phone
48840
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+61395944620
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Fax
48840
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Email
48840
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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
Windmill-task as a New Quantitative and Objective Assessment for Mirror Movements in Unilateral Cerebral Palsy: A Pilot Study.
2018
https://dx.doi.org/10.1016/j.apmr.2018.01.035
N.B. These documents automatically identified may not have been verified by the study sponsor.
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