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Trial registered on ANZCTR
Registration number
ACTRN12610000508077
Ethics application status
Approved
Date submitted
3/06/2010
Date registered
21/06/2010
Date last updated
6/09/2012
Type of registration
Prospectively registered
Titles & IDs
Public title
Intra-oral myofascial therapy compared to education and self care for chronic myogenous temporomandibular disorder. A randomised trial
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Scientific title
In patients with chronic myogenous temporomandibular disorder is manual therapy of the jaw muscles more effective than education and self care in decreasing pain and increasing interincisal opening range of the jaw?
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Secondary ID [1]
251947
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none
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Universal Trial Number (UTN)
U1111-1115-4495
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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 myogenous temporomandibular disorder
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Condition category
Condition code
Musculoskeletal
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0
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Other muscular and skeletal disorders
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Physical Medicine / Rehabilitation
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0
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Other physical medicine / rehabilitation
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Manual therapy (intra-oral myofascial manual therapy) of jaw muscles involving two treatments of 10-15 minutes duration each session per week for five weeks
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Intervention code [1]
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Rehabilitation
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Intervention code [2]
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Treatment: Other
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Comparator / control treatment
A short scripted dialogue of 10 minutes duration on jaw pain pathophysiology and anatomy administered face to face with a trained therapist, plus self care jaw exercises (demonstrated by the therapist during the first session and then the participant is monitored performing them once each session for a total of 5 sessions, once a week for 5 weeks). The exercises are also to be performed at home 2x daily for 5 minutes for the duration of the trial (5 weeks)
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Control group
Active
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Outcomes
Primary outcome [1]
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jaw pain on an 11 point graded chronic pain scale
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Assessment method [1]
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Timepoint [1]
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baseline, six weeks
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Secondary outcome [1]
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jaw opening range in mm using vernier calipers
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Assessment method [1]
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Timepoint [1]
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baseline, six weeks
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Eligibility
Key inclusion criteria
chronic jaw pain 3/10 or greater on a graded chronic pain scale of at least 3 months duration
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Minimum age
18
Years
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Maximum age
50
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
head and neck trauma, neoplasia of head and neck, edentulous patients, less than 3/10 on a graded chronic pain scale
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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)
enrollment by blinded receptionist, who contacted a volunteer who held the randomization schedule (computer generated) off premises
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
computer generated randomization schedule (www.randomizer.org)
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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
Completed
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Date of first participant enrolment
Anticipated
1/07/2010
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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
60
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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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Macquarie University
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Address [1]
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North Ryde NSW 2109
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Country [1]
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Australia
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Primary sponsor type
University
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Name
Macquarie University
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Address
North Ryde NSW 2109
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Country
Australia
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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]
256367
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Country [1]
256367
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Macquarie University Human Ethics Review Committee
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Ethics committee address [1]
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North Ryde NSW 2109
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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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04/06/2010
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Approval date [1]
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Ethics approval number [1]
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5201000771
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Summary
Brief summary
The primary purpose of the study is to test whether intra-oral myofascial therapy for chronic myogenous temporomandibular disorder is more effective than education and self care in the short term
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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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Allan Kalamir
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Address
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249 Edensor Road Edensor Park NSW 2176
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Country
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Australia
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Phone
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+61-2-98220066
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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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Allan Kalamir
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Address
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249 Edensor Road Edensor Park NSW 2176
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Country
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Australia
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Phone
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+61-2-98220066
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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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