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Trial registered on ANZCTR
Registration number
ACTRN12619001557123
Ethics application status
Approved
Date submitted
18/09/2019
Date registered
12/11/2019
Date last updated
8/06/2021
Date data sharing statement initially provided
12/11/2019
Type of registration
Prospectively registered
Titles & IDs
Public title
Evaluation of the ELEMENTS tablet for post-stroke rehabilitation
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Scientific title
Evaluation of the ELEMENTS tablet for rehabilitation of cognition and dexterity of the upper limb in post-stroke rehabilitation
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Secondary ID [1]
299173
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Nil known
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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:
stroke
314282
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Condition category
Condition code
Stroke
312631
312631
0
0
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Haemorrhagic
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Stroke
312632
312632
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0
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Ischaemic
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Physical Medicine / Rehabilitation
312997
312997
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0
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Occupational therapy
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
The study is comprised of two cohorts: (1) hospital or inpatient based rehabilitation patients and (2) community based rehabilitation patients.
Both cohorts will complete 30 min of individual therapy sessions (conventional or experimental), 3 times weekly, prescribed by a senior Occupational/Physical Therapist specialist. The inpatient cohort will complete the interventions for 4 weeks as an inpatient and then an additional 8 weeks once discharged into the community and will be supported by a Specialist Occupational/Physical Therapist if and when required. The community based cohort will complete 8 weeks of therapy only and participants allocated to this group will complete all the therapy sessions in their own homes.
For the experimental intervention we will use the ELEMENTS-T tablet, an electronic device containing a computer software providing a mix of goal-directed and exploratory upper-limb movement and cognitive interactive tasks. The software will provide exercises of moderate intensity. Adherence to the therapy program will be monitored and recorded online, participants will be contacted by phone if/when required. Participants will complete all therapy session in hospital (inpatient cohort) and later at home (Community based cohort).
For the conventional intervention we will use the Graded Repetitive Arm Supplementary Program (GRASP), an evidence based exercise program designed for Stroke patients at the University of British Columbia https://neurorehab.med.ubc.ca/grasp/. This program provides a moderately intensive level of exercises and focus on part practice of the upper limb addressing strength, dexterity and rang of motion.
Participants will keep track and evidence of adherence to this program on a table and will receive regular phone calls to assess and monitor adherence.
Both cohorts will receive initially a 30 minute education session from a Senior Therapist and will be expected to complete the prescribed tasks in a self directed manner thereafter if able. Those participants requiring assistance with set up will have access to this from a family member or therapist, however they will be expected to complete all tasks with little to no intervention from another.
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Intervention code [1]
315480
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Rehabilitation
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Intervention code [2]
315701
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Treatment: Devices
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Intervention code [3]
315702
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Treatment: Other
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Comparator / control treatment
The control/comparator group will complete conventional treatment plus GRASP for the same dosage as the intervention group (3 times weekly 30 minutes exercise sessions).
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Control group
Active
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Outcomes
Primary outcome [1]
321289
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Unilateral gross manual dexterity measured using the Box and Blocks Test (BBT)
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Assessment method [1]
321289
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Timepoint [1]
321289
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Baseline
Post-treatment (Inpatient Assessments) at 4 weeks post commencement of interventions.
Post treatment (Community Based assessments) at 8 weeks post commencement of interventions.
3-months follow up assessment
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Primary outcome [2]
321290
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Cognitive functioning as measured by the Montreal Cognitive Assessment (MoCA)
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Assessment method [2]
321290
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Timepoint [2]
321290
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Baseline
Post-treatment (Inpatient Assessments) at 4 weeks post commencement of interventions.
Post treatment (Community Based assessments) at 8 weeks post commencement of interventions.
3-months follow up assessment
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Primary outcome [3]
321440
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Stroke Impact Scale
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Assessment method [3]
321440
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Timepoint [3]
321440
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Baseline
Post-treatment (Inpatient Assessments) at 4 weeks post commencement of interventions.
Post treatment (Community Based assessments) at 8 weeks post commencement of interventions.
3-months follow up assessment
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Secondary outcome [1]
374537
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Finger dexterity as measured by the 9-Hole Peg Test
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Assessment method [1]
374537
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Timepoint [1]
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Baseline
Post-treatment (Inpatient Assessments) at 4 weeks post commencement of interventions.
Post treatment (Community Based assessments) at 8 weeks post commencement of interventions.
3-months follow up assessment
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Secondary outcome [2]
374538
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CogState Computerised Brief Battery
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Assessment method [2]
374538
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Timepoint [2]
374538
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Baseline
Post-treatment (Inpatient Assessments) at 4 weeks post commencement of interventions.
Post treatment (Community Based assessments) at 8 weeks post commencement of interventions.
3-months follow up assessment
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Secondary outcome [3]
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Degree of disability as measured by the Modified Rankin Scale (mRS)
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Assessment method [3]
374949
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Timepoint [3]
374949
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Baseline
Post-treatment (Inpatient Assessments) at 4 weeks post commencement of interventions.
Post treatment (Community Based assessments) at 8 weeks post commencement of interventions.
3-months follow up assessment
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Secondary outcome [4]
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Neurobehavioural Function Inventory (NFI)
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Assessment method [4]
374950
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Timepoint [4]
374950
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Baseline
Post-treatment (Inpatient Assessments) at 4 weeks post commencement of interventions.
Post treatment (Community Based assessments) at 8 weeks post commencement of interventions.
3-months follow up assessment
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Secondary outcome [5]
374951
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Utrecht Scale for Evaluation of Rehabilitation-Participation (USER-P)
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Assessment method [5]
374951
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Timepoint [5]
374951
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Baseline
Post-treatment (Inpatient Assessments) at 4 weeks post commencement of interventions.
Post treatment (Community Based assessments) at 8 weeks post commencement of interventions.
3-months follow up assessment
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Eligibility
Key inclusion criteria
1. Aged 18 years and above
2. English speaking
3. Sustained an ischemic or haemorrhagic stroke, subsequently confirmed on routine
neuroimaging
4. Admitted to the Rehabilitation Service of the Hospital (or respective hospital)
for treatment of identified upper limb rehabilitation needs
5. Able to provide informed consent
6. At least partial active anti-gravity upper limb movement at shoulder, elbow and forearm.
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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
1. Previous history of neurologic or psychiatric disorder
2. Pre-existent dementia (standardised cut-off of at least 3.6 on the short Informant Questionnaire on Cognitive Decline in the Elderly
3. Receptive aphasia preventing comprehension of instructions
4. Visual acuity deficit that prevents perception of visual material
5. Lack of a contact telephone to arrange follow-up
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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)
sealed opaque envelopes
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation using a randomisation table created by computer software (i.e. computerised sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people assessing the outcomes
The people analysing the results/data
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
Mixed-effects Analysis of Variance (ANOVA) will be used to compare the outcomes of participants (Conventional Treatment Group vs. Combined Treatment Group) at each time point (baseline, post-inpatient intervention/post-outpatient intervention, and 3-month follow-up). Correlation and hierarchical regression analyses will be used to identify and determine the impact of moderator/predictor variables on motor, cognitive, and functional outcomes. Finally, the effect sizes of primary and secondary outcome measures and 95% confidence intervals will be calculated.
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
18/11/2019
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Actual
25/11/2019
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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
32
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Accrual to date
19
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Final
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Recruitment in Australia
Recruitment state(s)
NSW
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Recruitment hospital [1]
14719
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Prince of Wales Hospital - Randwick
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Recruitment postcode(s) [1]
27759
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2031 - Randwick
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Funding & Sponsors
Funding source category [1]
303716
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Commercial sector/Industry
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Name [1]
303716
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AusIndustry
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Address [1]
303716
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Department of Industry, Innovation and Science,
GPO 2013,
Canberra, ACT, 2601.
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Country [1]
303716
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Australia
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Primary sponsor type
University
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Name
Australian Catholic University
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Address
115 Victoria Parade, Fitzroy Vic 3065
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Country
Australia
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Secondary sponsor category [1]
303830
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University
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Name [1]
303830
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University of Sydney
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Address [1]
303830
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The University of Sydney
Camperdown NSW 2050
Australia
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Country [1]
303830
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
304241
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South Eastern Sydney Local Health District - Human Research Ethics Committee
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Ethics committee address [1]
304241
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Room G71 East Wing,
Edmund Blacket Building
Prince of Wales Hospital
Randwick NSW 2031
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Ethics committee country [1]
304241
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Australia
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Date submitted for ethics approval [1]
304241
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Approval date [1]
304241
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05/03/2019
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Ethics approval number [1]
304241
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Summary
Brief summary
We anticipate that participants recovering from stroke will be able to participate in inpatient and home-based ELEMENTS-T therapy effectively and will show enhanced motivation to engage in therapy as a result of their involvement. This will fulfil the principle that rehabilitation methods that encourage intense interaction are most beneficial. With the ELEMENTS-T system, intensity is ‘given for free’ because the therapy is fun and the benefits accrue incidentally as a function of active and playful interaction. We expect that the user interaction afforded by the system will enable inpatients to make significant gains in motor and cognitive function, compared to treatment as usual.
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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
96250
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Dr Jeffrey Rogers
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Address
96250
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The University of Sydney
Camperdown NSW 2050
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Country
96250
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Australia
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Phone
96250
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+61 2 9351 9261
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Fax
96250
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Email
96250
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[email protected]
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Contact person for public queries
Name
96251
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Dr Jeffrey Rogers
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Address
96251
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The University of Sydney
Camperdown NSW 2050
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Country
96251
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Australia
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Phone
96251
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+61 2 9351 9261
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Fax
96251
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Email
96251
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[email protected]
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Contact person for scientific queries
Name
96252
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Dr Jeffrey Rogers
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Address
96252
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The University of Sydney
Camperdown NSW 2050
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Country
96252
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Australia
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Phone
96252
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+61 2 9351 9261
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Fax
96252
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Email
96252
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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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
Home-based (virtual) rehabilitation improves motor and cognitive function for stroke patients: a randomized controlled trial of the Elements (EDNA-22) system.
2021
https://dx.doi.org/10.1186/s12984-021-00956-7
N.B. These documents automatically identified may not have been verified by the study sponsor.
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