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Trial registered on ANZCTR
Registration number
ACTRN12614000085673
Ethics application status
Approved
Date submitted
15/01/2014
Date registered
23/01/2014
Date last updated
23/01/2014
Type of registration
Prospectively registered
Titles & IDs
Public title
Does targeted management of sub-acute back pain patients on a surgical clinic waiting list reduce chronic pain and disability? Phase 1: Risk screening.
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Scientific title
Risk-screening questionnaires provided to sub-acute back pain patients on a surgical clinic waiting list: does screening itself reduce chronic pain and disability?
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Secondary ID [1]
283909
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Nil
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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:
Back pain
290982
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Condition category
Condition code
Musculoskeletal
291259
291259
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0
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Other muscular and skeletal disorders
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Public Health
291327
291327
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0
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Health service research
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Participants will be initiallly contacted by telephone and will subsequently receive 3 questionnaires via mail to complete and return. These questionnaires aim to screen for risk of developing chronic pain and disability and will be evaluated for their usefulness in this patient group. Follow-up will occur after 4 months. Two of these questionnaires have been previously validated: (i) The Orebro Musculoskeltal Pain Screening Questionnaire (short version) and (ii) The STarT Back Screening Tool. The third screening tool - The 3 Item Screening Questionnaire, has been specifically developed for this study. All questionnaires are sent together at the initial timepoint.
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Intervention code [1]
288589
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Early detection / Screening
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Comparator / control treatment
Participants in the control group will not receive any screening questionnaires. They will be evaluated at the 4 month timepoint.
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Control group
Active
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Outcomes
Primary outcome [1]
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Pain Numeric Rating Scale score
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Assessment method [1]
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Timepoint [1]
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At 4 month follow up
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Primary outcome [2]
291256
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Disability Numeric Rating Scale score
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Assessment method [2]
291256
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Timepoint [2]
291256
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At 4 month follow-up
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Secondary outcome [1]
306352
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Roland Morris Disability Questionnaire
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Assessment method [1]
306352
0
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Timepoint [1]
306352
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4 month follow-up
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Secondary outcome [2]
306353
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Pain Catastrophising Scale
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Assessment method [2]
306353
0
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Timepoint [2]
306353
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4 month follow-up
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Secondary outcome [3]
306354
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Hospital Anxiety and Depression Score
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Assessment method [3]
306354
0
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Timepoint [3]
306354
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4 month follow-up
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Secondary outcome [4]
306355
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Pain-Self-Efficacy Questionnaire
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Assessment method [4]
306355
0
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Timepoint [4]
306355
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4 month follow-up
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Eligibility
Key inclusion criteria
Patients with sub-acute lumbar spine disorders who have been referred to the RAH Orthopaedic Spinal Outpatients, triaged (from documented referral information) and placed on a Spinal Outpatient Clinic waiting list.
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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
- Unable to speack and understand English (interpreter requested in referral)
- Previous lumbar spine surgery reported in referral
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Study design
Purpose of the study
Prevention
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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)
After satisfying the selection criteria (assessed from referral information provided) participants will be randomly assigned to the screening group or the control group. This will be achieved through central randomisation via computer.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation of participants will occur using a computer software generated randomisation table.
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Masking / blinding
Open (masking not 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
Efficacy
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Statistical methods / analysis
Sample size is based upon published variance measures for the primay outcome variables: 11 point (0-10) numerical rating scales for pain and disability. The pain measure shows the higher variance - the mean (SD) pain score for patients with subacute low back pain is 5.3 (2.2) and the limiting factor will be the comparison of those patients who are screened and those who are not. As such, in order to detect a 2 point difference between these groups and obtain likelihood ratios with acceptable confidence intervals, with an alpha of 0.005 and 80% power, we will need 196 patients.
The research team will continue to work with a biostatistician to formulate and analysis framework as the project progresses.
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
5/02/2014
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Actual
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Date of last participant enrolment
Anticipated
5/11/2014
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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
196
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
SA
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Recruitment hospital [1]
1968
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The Royal Adelaide Hospital - Adelaide
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Recruitment postcode(s) [1]
7700
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5000 - Adelaide
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Funding & Sponsors
Funding source category [1]
288549
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Hospital
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Name [1]
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Royal Adelaide Hospital
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Address [1]
288549
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North Terrace, Adelaide, SA, 5000
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Country [1]
288549
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Australia
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Primary sponsor type
Hospital
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Name
Royal Adelaide Hospital
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Address
North Terrace, Adelaide, SA, 5000
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Country
Australia
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Secondary sponsor category [1]
287261
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University
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Name [1]
287261
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University of South Australia
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Address [1]
287261
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GPO Box 2471, Adelaide, SA, 5000
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Country [1]
287261
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
290413
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Royal Adelaide Hospital Research Ethics Committee
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Ethics committee address [1]
290413
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North Terrace, Adelaide, SA, 5000
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Ethics committee country [1]
290413
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Australia
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Date submitted for ethics approval [1]
290413
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Approval date [1]
290413
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09/12/2013
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Ethics approval number [1]
290413
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131202
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Summary
Brief summary
This investigation involves the collection of data via postal questionnaires from patients with low back pain who have been placed on a waiting list for surgical opinion. The questionnaires aim to identify those at risk of developing chronic back pain and will be evaluated for their usefulness in this patient group. Additionally, this study will ask the question of whether screening itself reduces pain and disability. This investigation will lay the critical platform for an investigation of treatment aimed at reducing risk.
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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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Mrs Emma Karran
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Address
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Physiotherapy Department
Royal Adelaide Hospital
North Terrace
Adelaide
SA 5000
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Country
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Australia
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Phone
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61 8 82225334
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Emma Karran
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Address
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Physiotherapy Department
Royal Adelaide Hospital
North Terrace
Adelaide
SA 5000
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Country
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Australia
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Phone
45567
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61 8 82225334
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Fax
45567
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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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Emma Karran
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Address
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Physiotherapy Department
Royal Adelaide Hospital
North Terrace
Adelaide
SA 5000
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Country
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Australia
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Phone
45568
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61 8 82225334
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Fax
45568
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Email
45568
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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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