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Trial registered on ANZCTR
Registration number
ACTRN12612001016820
Ethics application status
Approved
Date submitted
19/09/2012
Date registered
20/09/2012
Date last updated
20/09/2012
Type of registration
Prospectively registered
Titles & IDs
Public title
Safety, feasibility and efficacy of a dance intervention for people with Parkinson's disease: a pilot study
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Scientific title
A randomised controlled trial of the safety and efficacy of a dance intervention compared to usual care on gait in people with Parkinson's disease
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Secondary ID [1]
281264
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Nil
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Universal Trial Number (UTN)
Nil
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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:
Idiopathic Parkinson's disease
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Condition category
Condition code
Neurological
287799
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0
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Parkinson's disease
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Physical Medicine / Rehabilitation
287806
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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
Participants will complete 1 hour weekly dance classes for 8 weeks, led by a professional dance instructor under guidance of experienced physiotherapists. Participants will also be asked to adhere to a 1 hour weekly home-based mental rehearsal program
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Intervention code [1]
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Rehabilitation
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Comparator / control treatment
Usual care control group. Particpants in this group will be able to continue with usual physiotherapy or exercise routines throughout the study
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Control group
Active
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Outcomes
Primary outcome [1]
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Feasibility assessed by adherence, safety, attrition and participant acceptibility. Safety will be assessed by monitoring and reporting any adverse events that occur during the 8 dance classes. Participant acceptibility information will be collected and assessed during an open focus group for the dance participants after the 8 weeks of dancing.
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Assessment method [1]
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Timepoint [1]
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Adherence, safety and attrition will be monitored and assessed for the 8 week interevention period. Participant acceptibility will be assessed at 8 weeks.
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Primary outcome [2]
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Gait speed measured by 6-meter walk test
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Assessment method [2]
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Timepoint [2]
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at baseline and at 8 week and 3 month follow-up assessments
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Secondary outcome [1]
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Functional mobility measured by the Timed-up and Go
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Assessment method [1]
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Timepoint [1]
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at baseline and at 8 week and 3 month follow-up assessments
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Secondary outcome [2]
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Balance measured by the Mini BESTest
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Assessment method [2]
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Timepoint [2]
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at baseline and at 8 week and 3 month follow-up assessments
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Secondary outcome [3]
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Self efficacy measured by the Ambulatory self-confidence questionnaire and the Activities-specific balance confidence scale
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Assessment method [3]
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Timepoint [3]
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at baseline and at 8 week and 3 month follow-up assessments
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Secondary outcome [4]
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Quality of life measured by the PDQ-39
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Assessment method [4]
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Timepoint [4]
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at baseline and at 8 week and 3 month follow-up assessments
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Eligibility
Key inclusion criteria
1. Diagnosed with idiopathic Parkinson's disease by a Neurologist
2. Living in the community/at home
3. Aged under 75 years of age
4. Between Hoehn and Yahr stage 1-3
5. Be medically safe to participate in an active exercise program, as assessed by the patients Neurologist, GP or other medical practitioner
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Minimum age
18
Years
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Maximum age
75
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. Unable to communicate in English
2. Have dementia, score less than 24 on the Mini Mental State Examination (MMSE) or are unable to provide informed consent
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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)
A blinded independent person will assign participants with sealed opaque envelopes
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
An independent person will randomly allocate participants using a computer generated number sequence
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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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
Safety/efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
15/10/2012
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Actual
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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
20
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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]
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University
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Name [1]
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La Trobe University
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Address [1]
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La Trobe University
Plenty Road
Bundoora, VIC 3086
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Country [1]
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Australia
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Primary sponsor type
Individual
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Name
Prof Meg Morris
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Address
Faculty of Health Sciences
La Trobe University
Bundoora, VIC 3086
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Country
Australia
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Secondary sponsor category [1]
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Individual
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Name [1]
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Dr Jenny McGinley
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Address [1]
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The University of Melbourne
200 Berkeley Street
Carlton, VIC 3010
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Country [1]
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Australia
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Other collaborator category [1]
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Individual
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Name [1]
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Rebecca Twyerould
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Address [1]
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The University of Melbourne
200 Berkeley Street
Carlton, VIC 3010
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Country [1]
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Behavioral and Social Sciences Human Ethics sub-committee
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Ethics committee address [1]
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Human Research Ethics Level 5, Alan Gilbert Building, 161 Barry St Carlton, VIC 3053
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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Approval date [1]
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19/09/2012
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Ethics approval number [1]
288082
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1237989
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Summary
Brief summary
The aim of this pilot study is to explore the feasibility and efficacy of a rehabilitative dance intervention designed to reduce disability and to improve quality of life in a small sample of adults with Parkinson’s disease. Twenty adults with PD will be recruited and randomly allocated to either a usual care group or an 8-week dance intervention. Gait, balance and quality of life will be measured in all participants at baseline, 8 weeks and 3 months. Additionally, the intervention will be assessed for feasibility in terms of adherence, attrition safety and participant acceptability. The results of this study are designed to inform and verify the methodology for a larger subsequent RCT and to determine the feasibility of dancing for a small group of people with PD
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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
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Prof Meg Morris
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Address
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Faculty of Health Sciences La Trobe University
Bundoora, VIC 3086
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Country
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Australia
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Phone
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+61 3 9479 6080
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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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Prof Meg Morris
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Address
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Faculty of Health Sciences La Trobe University
Bundoora, VIC 3086
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Country
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Australia
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Phone
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+61 3 9479 6080
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Fax
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Email
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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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