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Trial registered on ANZCTR
Registration number
ACTRN12617000122358
Ethics application status
Approved
Date submitted
17/01/2017
Date registered
24/01/2017
Date last updated
23/06/2021
Date data sharing statement initially provided
23/06/2021
Date results provided
23/06/2021
Type of registration
Prospectively registered
Titles & IDs
Public title
Can thinking about movement improve movement speed in older adults?
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Scientific title
Motor learning with motor imagery training: within session effects of motor imagery training in healthy older adults
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Secondary ID [1]
290941
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Nil known
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Universal Trial Number (UTN)
U1111-1191-7495
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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:
Elderly
301670
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Mobility
301671
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Condition category
Condition code
Physical Medicine / Rehabilitation
301378
301378
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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
Arm 1:
Kinesthetic motor imagery
Participants will be instructed to imagine themselves performing a previoulsy performed mobility task. The mobility task involves getting out of a chair, walking 10m, stepping over a step, going through a series of markers that require small changes of direction, then turning around 90 degrees, returning through markers, over step, walk a further 10m and return to sitting. This task includes a number of mobility related components essential for safe ambulation in older adults.
Participants will perform 20 imagined repetitions of a the mobility task over a period of 20 minutes with a 30second rest between each repetition. All repetitions will be completed within a single session.
Motor imagery training will be supervised by a physiotherapist with over 10 years experience
Arm 2:
Physical practice
Participants will be instructed to physically perform the combined mobility task. The mobility task involves getting out of a chair, walking 10m, stepping over a step, going through a series of markers that require small changes of direction, then turning around 90 degrees, returning through markers, over step, walk a further 10m and return to sitting. This task includes a number of mobility related components essential for safe ambulation in older adults.
Participants will perform 20 repetitions of the mobility task over a period of approximately 20minutes, with 30 seconds rest between repetitions. All repetitions will be completed within a single session.
The physical practice will be supervised by a physiotherapist with over 10 years experience
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Intervention code [1]
296880
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Treatment: Other
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Comparator / control treatment
They will be occupied watching/playing on an electronic device (iPad) for the equivalent time (~20minutes) as those involved in the motor imagery and physical training. Participants can choose from a small selection of games that require them to complete maths or language based problems. As such they will be required to concentrate but it is not anticipated to have any treatment value.
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Control group
Placebo
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Outcomes
Primary outcome [1]
300771
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Timed to complete the Combined mobility task once
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Assessment method [1]
300771
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Timepoint [1]
300771
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Baseline and immediately after training or control session
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Primary outcome [2]
300772
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Timed up and go
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Assessment method [2]
300772
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Timepoint [2]
300772
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Basleline and immediately after training or control session
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Secondary outcome [1]
330825
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Imagined timed up and go
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Assessment method [1]
330825
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Timepoint [1]
330825
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Baseline and immediately after training or control session
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Secondary outcome [2]
343430
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Gait variability is assessed on the GaitRite mat. The mat detects foot placements during gait.
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Assessment method [2]
343430
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Timepoint [2]
343430
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Baseline and immediately after training or control session
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Eligibility
Key inclusion criteria
independently mobile
can commit to the study time frames
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Minimum age
65
Years
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Maximum age
85
Years
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
any falls in the past 12 months
require a walking aid for indoor mobility
acute or terminal illness
unstable cardiovascular and/or respiratory disorder
neurological disease
joint replacement in the past six months.
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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 envelope
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computerised sequence generation
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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
This is a feasability study that will inform sample size calculations for furture interventions.
Analysis of variance will be used to determine whether changes from baseline to follow-up assessment are different between groups for primary outcome variables
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/02/2017
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Actual
7/02/2017
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Date of last participant enrolment
Anticipated
27/06/2017
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Actual
20/07/2017
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Date of last data collection
Anticipated
30/06/2017
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Actual
1/08/2017
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Sample size
Target
20
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Accrual to date
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Final
30
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Recruitment in Australia
Recruitment state(s)
QLD
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Recruitment postcode(s) [1]
15109
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4014 - Banyo
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Funding & Sponsors
Funding source category [1]
295359
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University
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Name [1]
295359
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Australian Catholic University
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Address [1]
295359
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1100 Nudgee Road Banyo QLD 4014
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Country [1]
295359
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Australia
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Primary sponsor type
Individual
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Name
Vaughan Nicholson
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Address
School of Physiotherapy
Australian Catholic University
1100 Nudgee Road Banyo QLD 4014
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Country
Australia
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Secondary sponsor category [1]
294184
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None
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Name [1]
294184
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Address [1]
294184
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Country [1]
294184
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
296691
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Australian Catholic University Human Research Ethics Committee
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Ethics committee address [1]
296691
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Australian Catholic University North Sydney Campus PO Box 968 NORTH SYDNEY, NSW 2059
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Ethics committee country [1]
296691
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Australia
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Date submitted for ethics approval [1]
296691
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14/11/2016
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Approval date [1]
296691
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03/01/2017
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Ethics approval number [1]
296691
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2016-285H
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Summary
Brief summary
Motor imagery is an imagining of an action without its physical execution; it is a dynamic state during which the representation of a given motor act is internally rehearsed or imagined within working memory without any overt muscle activation. Motor imagery activates brain regions that are activated during actual task performance and motor imagery training has been found to improve task performance. Motor imagery has been found to improve static balance in the elderly but its effect on dynamic balance or functional performance in older adults is unknown. The aim of this study is to determine whether imagining certain movements repeatedly promotes improvements in mobility. It is hypothesised that motor imagery will improve mobility but a point of diminishing gains will occur after multiple repetitions.
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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
71794
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Dr Vaughan Nicholson
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Address
71794
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School of Physiotherapy
Australian Catholic University, Brisbane Campus
1100 Nudgee Rd Banyo QLD 4014
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Country
71794
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Australia
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Phone
71794
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+61 7 36237687
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Fax
71794
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Email
71794
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[email protected]
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Contact person for public queries
Name
71795
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Vaughan Nicholson
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Address
71795
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School of Physiotherapy
Australian Catholic University, Brisbane Campus
1100 Nudgee Rd Banyo QLD 4014
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Country
71795
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Australia
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Phone
71795
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+61 7 36237687
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Fax
71795
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Email
71795
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[email protected]
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Contact person for scientific queries
Name
71796
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Vaughan Nicholson
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Address
71796
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School of Physiotherapy
Australian Catholic University, Brisbane Campus
1100 Nudgee Rd Banyo QLD 4014
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Country
71796
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Australia
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Phone
71796
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+61 7 36237687
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Fax
71796
0
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Email
71796
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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?
all of the individual participant data collected during the trial, after de-identification
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When will data be available (start and end dates)?
ending 5 years following main results publication
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Available to whom?
researchers who provide a methodologically sound proposal
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Available for what types of analyses?
any purpose
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How or where can data be obtained?
access subject to approvals by Principal Investigator -
[email protected]
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What supporting documents are/will be available?
No Supporting Document Provided
Doc. No.
Type
Citation
Link
Email
Other Details
Attachment
12208
Ethical approval
[email protected]
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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