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Trial registered on ANZCTR
Registration number
ACTRN12615000580572
Ethics application status
Approved
Date submitted
15/05/2015
Date registered
3/06/2015
Date last updated
16/02/2017
Type of registration
Retrospectively registered
Titles & IDs
Public title
The effectiveness of functional motor control exercise training in patients with chronic low back pain
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Scientific title
The effectiveness of functional motor control exercise training versus general exercise on movement control ability, pain intensity, disability in patients with chronic low back pain
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Secondary ID [1]
286711
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None
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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:
Chronic low back pain
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Condition category
Condition code
Musculoskeletal
295318
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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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Physiotherapy
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Functional motor control exercise including core muscle strengthening, spine segmental control, trunk and extremity dissociated movement control retraining will be administered by a physiotherapist. Participants in this group will receive 16 one-to-one sessions (45 minutes/session), twice a week for 8 weeks.
The exercise programs will be tailored to individual patient. Outcome will be assessed upon completion of the 8-week program and at 6-week follow-up after the treatment.
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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
General exercise will include trunk and extremity strengthening, stretching exercises. Each patient will receive at least 10 sessions (30 minutes/session) of treatment in 8 weeks. The program will be one-to-one sessions with a physiotherapist. The maximum number of sessions that may be administered is 16.
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Control group
Active
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Outcomes
Primary outcome [1]
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Movement control ability assessed by a battery of movement control tests including 7 flexion control tests and 7 extension control tests
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Assessment method [1]
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Timepoint [1]
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baseline, upon completion of 8-week training, 6-week follow-up
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Primary outcome [2]
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Psychological impairment: Fear avoidance beliefs questionnaire (FABQ)
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Assessment method [2]
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Timepoint [2]
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baseline, upon completion of 8-week training, 6-week follow-up
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Secondary outcome [1]
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Pain intensity: Numeric rating scale
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Assessment method [1]
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Timepoint [1]
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baseline, upon completion of 8-week training, 6-week follow-up
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Secondary outcome [2]
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Disability: Oswestry low back pain disability questionnaire
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Assessment method [2]
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Timepoint [2]
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baseline, upon completion of 8-week training, 6-week follow-up
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Secondary outcome [3]
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Movement confidence: Low back activity confidence scale (LoBACS)
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Assessment method [3]
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Timepoint [3]
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baseline, upon completion of 8-week training, 6-week follow-up
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Secondary outcome [4]
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Perceived improvement: Global rating of change scale (GRoCS)
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Assessment method [4]
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Timepoint [4]
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upon completion of 8-week training, 6-week follow-up
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Secondary outcome [5]
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Function: Patient specific functional scale (PSFS)
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Assessment method [5]
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Timepoint [5]
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baseline, upon completion of 8-week training, 6-week follow-up
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Secondary outcome [6]
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Physical performance: Repeated sit-to-stand test
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Assessment method [6]
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Timepoint [6]
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baseline, upon completion of 8-week training, 6-week follow-up
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Eligibility
Key inclusion criteria
1. Aged 20-65 patients with chronic low back pain (more than 3 months)
2. Pain intensity (numeric rating scale) > 4/10
3. No lower extremity symptoms
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Minimum age
20
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
1. Tumor
2. Spinal/lower extremity surgery
3. Osteoporosis
4. Hip/knee osteoarthritis
5. Pregnancy
6. Experiencing any of the spinal inflammatory diseases (such as ankylosing spondylitis, rheumatoid arthritis)
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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
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
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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
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/07/2014
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Actual
25/07/2014
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Date of last participant enrolment
Anticipated
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Actual
8/09/2015
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Date of last data collection
Anticipated
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Actual
15/01/2016
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Sample size
Target
60
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Accrual to date
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Final
52
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Recruitment outside Australia
Country [1]
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Taiwan, Province Of China
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State/province [1]
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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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Wendy Tzyy-Jiuan Wang
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Address [1]
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155, Sec. 2, Li-Nong St.
Beitou District, Taipei 11221
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Country [1]
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Taiwan, Province Of China
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Primary sponsor type
University
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Name
National Yang-Ming University
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Address
155, Sec. 2, Li-Nong St.
Beitou District, Taipei 11221
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Country
Taiwan, Province Of China
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Secondary sponsor category [1]
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Hospital
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Name [1]
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Cheng Hsin General Hospital
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Address [1]
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No.45, Cheng Hsin St., Baitou District, Taipei, 11220
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Country [1]
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Taiwan, Province Of China
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Institutional Review Board of Cheng Hsin General Hospital
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Ethics committee address [1]
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No. 45, Cheng Hsin St., Baitou District, Taipei, 11220
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Ethics committee country [1]
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Taiwan, Province Of China
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Date submitted for ethics approval [1]
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Approval date [1]
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01/07/2014
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Ethics approval number [1]
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Summary
Brief summary
Our study purpose is to compare the improvement of movement control ability and clinical outcomes in patients with chronic low back pain after functional motor control exercise training. Our hypothesis is that patients in the functional motor control exercise group will demonstrate better improvement of movement control ability and clinical outcomes than those in the general exercise group.
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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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A/Prof Wendy Tzyy-Jiuan Wang
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Address
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155, Sec. 2, Li-Nong St. Beitou District, Taipei, 11221
National Yang-Ming University
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Country
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Taiwan, Province Of China
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Phone
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+886228267091
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Fax
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+886228201841
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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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Wendy Tzyy-Jiuan Wang
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Address
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155, Sec. 2, Li-Nong St. Beitou District, Taipei 11221
National Yang-Ming University
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Country
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Taiwan, Province Of China
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Phone
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+886228267091
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Fax
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+886228201841
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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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Wendy Tzyy-Jiuan Wang
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Address
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155, Sec. 2, Li-Nong St. Beitou District, Taipei, 11221
National Yang-Ming University
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Country
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Taiwan, Province Of China
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Phone
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+886228267091
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Fax
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+886228201841
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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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