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Trial registered on ANZCTR
Registration number
ACTRN12619001688178
Ethics application status
Approved
Date submitted
24/09/2019
Date registered
2/12/2019
Date last updated
2/12/2019
Date data sharing statement initially provided
2/12/2019
Type of registration
Retrospectively registered
Titles & IDs
Public title
Virtual reality based training for subjects with stroke
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Scientific title
Virtual reality training using X-Box Kinect in stroke subjects
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Secondary ID [1]
299394
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None
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Universal Trial Number (UTN)
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Trial acronym
SRT
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Stroke
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Balance
314568
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Functional independence
314569
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Reduced Mobility
314570
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Risk of fall
314571
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Condition category
Condition code
Stroke
312908
312908
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0
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Haemorrhagic
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Stroke
312909
312909
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0
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Ischaemic
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Physical Medicine / Rehabilitation
312910
312910
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0
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Physiotherapy
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
X-Box Kinect training for 30 minutes, three times a week for 8 weeks. The participants will play X-Box Kinect based games under supervision of qualified physiotherapist. X-Box kinect comes with a body motion sensor and allows the subject to play games and do exercises in virtual environment. The subjects would be reminded to come for their session via text messages.
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Intervention code [1]
315649
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Rehabilitation
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Comparator / control treatment
Balance training exercises: Tandem walk, high step walk, walking sideways, walking with alternate arm raise (Each with 10-15 steps in every session, having 3 sessions a week for 8 weeks)
Upper limb strengthening exercises: Straight push, circle movements, punching movement, pushing, unweighted and weighted bicep curls,side arm raise, overhead press. (Each with 10-12 repetitions with 2-3 minutes rest time between exercises to avoid fatigue in one session, 3 sessions will be given in a week for 8 weeks))
Core strengthening exercises: Trunk rotations, trunk lateral flexion, leg rotations, leg raise, bridges, crunches, knee to chest, Toe taps. (Each with 10-12 repetitions with 2-3 minutes rest time between exercises to avoid fatigue in one sessions, 3 sessions per week will be given for 8 weeks)
The interventions would be provided by qualified physiotherapist in safe environment.
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Control group
Active
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Outcomes
Primary outcome [1]
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Balance by using Berg Balance Scale
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Assessment method [1]
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Timepoint [1]
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Before receiving intervention and after 8 weeks of commencement of intervention
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Primary outcome [2]
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Fall risk assessment by using Morse fall assessment scale
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Assessment method [2]
321513
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Timepoint [2]
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Before starting intervention and after 8 weeks of commencement of intervention
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Primary outcome [3]
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Functional independence by functional independence measure
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Assessment method [3]
321514
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Timepoint [3]
321514
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Before starting intervention and after 8 weeks of commencement of intervention
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Secondary outcome [1]
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Mobility level by using timed up and go test
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Assessment method [1]
375195
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Timepoint [1]
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Before starting the intervention and after 8 weeks of commencement of intervention
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Eligibility
Key inclusion criteria
Vitally stable subjects who suffered stroke at least 3 months ago, with mild to moderately affected upper limb functions,
Berg balance score 21-40 and independent standing for at least 10 seconds.
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Minimum age
45
Years
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Maximum age
65
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
Subjects undergone any surgical procedures and suffering from other systemic diseases.
Presence of synergy patterns
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Study design
Purpose of the study
Educational / counselling / training
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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 randomization using sealed opaque envelopes
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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
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Statistical methods / analysis
Data will be analysed by SPSS 21, parametric and non parametric tests would be used accordingly to get the results
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
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Actual
2/09/2019
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Date of last participant enrolment
Anticipated
30/11/2019
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Actual
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Date of last data collection
Anticipated
14/12/2019
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Actual
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Sample size
Target
50
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Accrual to date
46
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Final
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Recruitment outside Australia
Country [1]
21884
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Pakistan
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State/province [1]
21884
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Islamabad Capital Territory
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Funding & Sponsors
Funding source category [1]
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Hospital
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Name [1]
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Shifa International Hospital
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Address [1]
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Rehabilitation department, Shifa International Hospital, H8/4 Islamabad
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Country [1]
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Pakistan
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Primary sponsor type
Individual
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Name
Nasir Sultan
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Address
Rehabilitation Department, Shifa international Hospital, H8/4, Islamabad
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Country
Pakistan
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Secondary sponsor category [1]
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Individual
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Name [1]
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Kiran Khushnood
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Address [1]
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Department of Physical Therapy, Shifa Tameer-e-Millat University, H8/4 Islamabad
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Country [1]
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Pakistan
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Institutional Review Board and Ethics Committee, Shifa International Hospital
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Ethics committee address [1]
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Shifa International Hospital, H-8/ 4, Islamabad
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Ethics committee country [1]
304409
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Pakistan
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Date submitted for ethics approval [1]
304409
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12/06/2019
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Approval date [1]
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04/07/2019
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Ethics approval number [1]
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IRB# 169-659-2019
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Summary
Brief summary
Stroke is one of the leading pathology that has high morbidity and mortality and is more prevalent in developing countries. Several intervention strategies have been and are being used to counter the symptoms and complications of stroke. Virtual reality is the trend for the era of rehabilitation and has been experimented a lot upon since last decade. Evidences have also shown its positive effects on stroke subjects. Effects and duration for outcome depends upon the type of device used and frequency of usage. Upper limb functions and balance can be improved by virtual reality in stroke patients. Xbox Kinect is a virtual reality device that can be used to improve physical activity along with whole body movements in stroke subjects. Evidence supports use of Xbox Kinect for improving postural control and balance in stroke patients. The proposed study would use Xbox Kinect to improve functional independence, balance, mobility and to reduce risk of fall in subjects with stroke.
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Trial website
None
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Trial related presentations / publications
None
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Public notes
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Contacts
Principal investigator
Name
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Mr Nasir Sultan
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Address
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Rehabilitation Department, Shifa International Hospital, H-8/4, Islamabad
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Country
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Pakistan
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Phone
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+92 321 9804117
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Kiran Khushnood
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Address
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Department of Physical Therapy, Shifa Tameer-e-Millat University, H-8/1, Islamabad
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Country
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Pakistan
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Phone
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+92 333 5993417
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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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Kiran Khushnood
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Address
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Department of Physical Therapy, Shifa Tameer-e-Millat University, H-8/1, Islamabad
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Country
96852
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Pakistan
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Phone
96852
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+92 333 5993417
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Fax
96852
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Email
96852
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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)?
Yes
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What data in particular will be shared?
Individual participant data underlying published results only
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When will data be available (start and end dates)?
Immediately following publication with no end date
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Available to whom?
Healthcare professionals, students and organizations working on stroke and it's rehabilitation
Researchers working on stroke rehabilitation
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Available for what types of analyses?
IPD meta-analysis
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How or where can data be obtained?
access subject to approvals by Principal Investigator
Email:
[email protected]
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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
No additional documents have been identified.
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