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Trial registered on ANZCTR
Registration number
ACTRN12607000458437
Ethics application status
Approved
Date submitted
29/08/2007
Date registered
11/09/2007
Date last updated
12/10/2010
Type of registration
Prospectively registered
Titles & IDs
Public title
Telephone coaching for return to usual activity.
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Scientific title
Randomised control trial of telephone coaching versus usual care in non-chronic non-specific low back pain to reduce activity limitation
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Secondary ID [1]
252856
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Telephone coaching for return to usual activity.
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Universal Trial Number (UTN)
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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:
Non-specific low back pain (NSLBP)
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Condition category
Condition code
Musculoskeletal
2408
2408
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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
Telephone-based health coaching in addition to usual physiotherapy care. Coaching will assess the importance of return to usual activity for the participant and if necessary use motivational interviewing and cognitive behavioural techniques to increase the importance. Coaching will also assess the participant's confidence to return to usual activities and apply goal setting and action plans to increase confidence to return. Particiapants will be coached once per week for four weeks and once three weeks after the fourth session. Each coaching session will last approximately 30 minutes.
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Intervention code [1]
2029
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Treatment: Other
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Comparator / control treatment
Usual care physiotherapy treatment (including referral to other health care services) as deemed necessary by the treating physiotherapist.
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Control group
Active
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Outcomes
Primary outcome [1]
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Mean difference on Oswestry disability index
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Assessment method [1]
3306
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Timepoint [1]
3306
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Baseline, 4, 12 weeks after randomisation.
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Primary outcome [2]
3307
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Mean difference on modified Patient Specific Functional scale
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Assessment method [2]
3307
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Timepoint [2]
3307
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Baseline, 4, 12 weeks after randomisation
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Secondary outcome [1]
5508
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Mean difference on pain Self Efficacy Questionnaire
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Assessment method [1]
5508
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Timepoint [1]
5508
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Baseline, 4, 12 weeks after randomisation.
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Secondary outcome [2]
5509
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Mean difference on Kessler 10 questionnaire
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Assessment method [2]
5509
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Timepoint [2]
5509
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Baseline, 4, 12 weeks after randomisation.
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Secondary outcome [3]
5510
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Number of physiotherapy treatment sessions
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Assessment method [3]
5510
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Timepoint [3]
5510
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12 weeks after randomisation.
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Secondary outcome [4]
5511
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Mean difference in recovery expectation for return to usual activity
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Assessment method [4]
5511
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Timepoint [4]
5511
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Baseline, 4, 12 weeks after randomisation.
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Eligibility
Key inclusion criteria
NSLBP for less than 8 weeks duration (first or new episode). Recovery expectation less than 8 out of 10 for return to all activities in next month. English speaking. Access to telephone.
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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
Low back pain due to a specific pathology NSLBP episode longer than 8 weeks. Histroy of surgery for back pain
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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)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
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Type of endpoint/s
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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
1/11/2007
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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
30
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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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Bundoora VIC 3086
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Country [1]
2568
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Australia
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Primary sponsor type
Individual
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Name
Ross Iles
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Address
School of Physiotherapy
La Trobe University
Bundoora VIC 3086
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Country
Australia
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Secondary sponsor category [1]
2323
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Individual
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Name [1]
2323
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Professor Nicholas Taylor
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Address [1]
2323
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School of Physiotherapy
La Trobe University
Bundoora VIC 3086
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Country [1]
2323
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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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La Trobe University Human Ethics Committee
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Ethics committee address [1]
4489
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La Trobe University Bundoora Victoria Australia 3086
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Ethics committee country [1]
4489
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Australia
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Date submitted for ethics approval [1]
4489
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03/09/2007
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Approval date [1]
4489
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27/09/2007
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Ethics approval number [1]
4489
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FHEC07/166
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Ethics committee name [2]
259854
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Eastern Health Researc and Ethics Committee
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Ethics committee address [2]
259854
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Level 2, Clive Ward Centre 16 Arnold St Box Hill Australia 3128
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Ethics committee country [2]
259854
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Australia
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Date submitted for ethics approval [2]
259854
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13/02/2008
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Approval date [2]
259854
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13/02/2008
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Ethics approval number [2]
259854
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E21/0708
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Summary
Brief summary
This study will examine whether adding telephone coaching (named BackReady coaching) intervention when added to usual physiotherapy care leads to a decrease in activity limitation in people at risk for long term activity limitation in non-specific low back pain. It is anticiapted that BackReady coaching will lead to a decrease in activity limitation and a greater number of participants returning to their primary non-leisure activity.
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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
28015
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Country
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Phone
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Fax
28015
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Email
28015
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Contact person for public queries
Name
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Ross Iles
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Address
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School of Physiotherapy
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 94795851
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Fax
11172
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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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Ross Iles
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Address
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School of Physiotherapy
La Trobe University
Bundoora VIC 3086
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Country
2100
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Australia
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Phone
2100
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+61 3 94795851
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Fax
2100
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Email
2100
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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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