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Trial registered on ANZCTR
Registration number
ACTRN12612000304831
Ethics application status
Approved
Date submitted
15/03/2012
Date registered
16/03/2012
Date last updated
31/07/2012
Type of registration
Prospectively registered
Titles & IDs
Public title
To investigate the effects of spinal manipulation for Achilles tendinopathy; a pilot study
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Scientific title
To investigate the effects of spinal manipulation for Achilles tendinopathy; a pilot study
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Secondary ID [1]
280139
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Nil
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Universal Trial Number (UTN)
U1111-1129-1365
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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:
chronic Achilles tendinopathy
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Condition category
Condition code
Injuries and Accidents
286260
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0
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Other injuries and accidents
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Musculoskeletal
286262
286262
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0
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Other muscular and skeletal disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
The intervention is a high velocity, low amplitude thrust manipulation, applied to the mid part of the spine (thoracic spine). It will take approximately 2 minutes to position the volunteer for this manipulation, and will take seconds to deliver the thrust. Volunteers will receive the manipulation during each physiotherapy appointment (i.e. twice weekly, for a total of 4 weeks).
The physiotherapy appointments will take about 20 minutes each, and during this time eccentric exercises will be monitored and modified as appropriate, and secondary outcome measures (blood pressure and pulse rate) will also be recorded.
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Intervention code [1]
284473
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Rehabilitation
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Comparator / control treatment
The comparator group will receive eccentric exercises only. Eccentric exercises are a special type of exercise known to be beneficial for the rehabilitation of Achilles tendinopathy. For both groups, these exercises will be completed twice daily, for a total of four weeks. All participants will receive education and an information sheet, outlining how these exercises are to be preformed. The comparator group will attend for physiotherapy twice weekly, for four weeks. During these 20 minute appointments they will receive education on the exercise regime, and secondary outcome measures (blood pressure and pulse rate) will be recorded.
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Control group
Active
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Outcomes
Primary outcome [1]
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The Victorian Institute of Sports Assessment - Achilles questionnaire (VISA-A) score will be the primary outcome. This questionnaire is designed to assess Achilles tendinopathy severity.
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Assessment method [1]
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Timepoint [1]
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Measures will be assessed before the initial intervention and after the final physiotherapy appointment, at the end of 4 weeks
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Primary outcome [2]
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The numeric pain rating scale (NPRS) will be the other primary measure taken. The scale assesses the intensity of pain.
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Assessment method [2]
286726
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Timepoint [2]
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Measures will be assessed before the initial intervention and during each physiotherapy appointment, for 4 consecutive weeks. This outcome measure will also be taken after the final physiotherapy appointment, at the end of 4 weeks.
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Secondary outcome [1]
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Blood pressure and pulse rate will be measured using an electronic blood pressure cuff.
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Assessment method [1]
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Timepoint [1]
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Twice weekly for the first four weeks.
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Eligibility
Key inclusion criteria
18-65 years old; diagnosis chronic AT by an advanced physiotherapist (i.e. post graduate practitioner); available twice weekly for a 20 minute physiotherapy appointment over 4 consecutive weeks.
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Minimum age
18
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
Contraindications to spinal manipulation such as osteoprosis, rheumatoid arthritis or the presence of cancer; bilateral tendinopathy involvement; Scheuermanns disease; neurological disease; pregnancy; inability to understand intervention or protocol.
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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)
Volunteers will be recruited through an advertisement in the local paper. The lead investigator will assess volunteers against the inclusion and exclusion criteria. Concealed allocation will be carried out; volunteers will be asked to draw from 20 sealed opaque envelopes. The envelopes will contain the volunteers number and allocation group. The clinic receptionist will then organise the volunteer’s appointments for the following 4 weeks.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
computerized sequence generation
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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
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
17/07/2012
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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 outside Australia
Country [1]
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New Zealand
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State/province [1]
4204
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Dunedin
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Funding & Sponsors
Funding source category [1]
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Self funded/Unfunded
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Name [1]
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Address [1]
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Country [1]
284889
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Primary sponsor type
Individual
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Name
Laura Kingston
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Address
School of Physiotherapy
University of Otago
PO Box 56
Dunedin
9045
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Country
New Zealand
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
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Country [1]
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New Zealand
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Other collaborator category [1]
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Individual
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Name [1]
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Dr. Steve Tumilty
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Address [1]
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School of Physiotherapy
University of Otago
PO Box 56
Dunedin
9045
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Country [1]
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New Zealand
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Other collaborator category [2]
260622
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Individual
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Name [2]
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Dr. Leica Claydon
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Address [2]
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School of Physiotheraoy
University of Otago
PO BOx 56
Dunedin
9045
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Country [2]
260622
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New Zealand
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Other collaborator category [3]
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Individual
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Name [3]
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Professor David Baxter
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Address [3]
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School of Physiotherapy University of Otago PO Box 56 Dunedin 9045
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Country [3]
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New Zealand
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
286886
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New Zealand Health and Disability Ethics Committee - Lower South Regional Ethics Committee
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Ethics committee address [1]
286886
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Ministry of Health No 1 The Terrace PO Box 5013 Wellington
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Ethics committee country [1]
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New Zealand
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Date submitted for ethics approval [1]
286886
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24/04/2012
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Approval date [1]
286886
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21/06/2012
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Ethics approval number [1]
286886
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Summary
Brief summary
The goal of this trial is to assess if spinal manipulation, in addition to eccentric exercises, has an impact on the functional recovery of Achilles tendinopathy. The hypothesis is that both groups will improve after 4 weeks of eccentric exercises, and that the intervention group (receiving the spinal manipulation), will improve more than the group receiving eccentric exercises alone.
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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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Laura Kingston
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Address
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School of Physiotherapy
University of Otago
PO Box 56
Dunedin 9054
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Country
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New Zealand
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Phone
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N/A
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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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Laura Kingston
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Address
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School of Physiotherapy
University of Otago
PO Box 56
Dunedin 9054
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Country
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New Zealand
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Phone
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N/A
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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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