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Trial registered on ANZCTR
Registration number
ACTRN12617001284358
Ethics application status
Approved
Date submitted
30/08/2017
Date registered
6/09/2017
Date last updated
22/12/2021
Date data sharing statement initially provided
13/11/2019
Date results provided
22/12/2021
Type of registration
Prospectively registered
Titles & IDs
Public title
Can an allied health and nursing expanded scope Treatment Access Pathway (TAP) improve health outcomes for people with persistent pain? A pragmatic randomised controlled trial
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Scientific title
Can an allied health and nursing expanded scope Treatment Access Pathway (TAP) improve health outcomes for people with persistent pain? A pragmatic randomised controlled trial
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Secondary ID [1]
292463
0
None
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Universal Trial Number (UTN)
U1111-1199-4668
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Trial acronym
TAP RCT
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Persistent Pain
304080
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Condition category
Condition code
Public Health
303416
303416
0
0
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Health service research
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Physical Medicine / Rehabilitation
303417
303417
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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
A pragmatic randomised controlled trial design will be employed - analysis and comparison of cross over waitlist group outcomes. The proposed study has two separate study areas. The first part of the project will compare treatment from day 1 of referral (TAP without wait) to a waitlist control (Waitlist). This will provide data on clinical outcomes of treatment versus no treatment. Participants who are allocated to the treatment group (TAP without wait) will enter the TAP pathway and receive treatment. At six months, participants in the treatment group will attend an appointment with a research assistant to re-collect the measures that were administered at time 1.. This study will not directly address the question of whether TAP is effective if delivered, as it will be in routine practice, after several months of waiting for treatment (i.e., following the decline in functioning and increased pain that occurs after 6 months of waiting for treatment). This study limitation, and associated critique that RCT TAP outcomes may be inflated due to earlier treatment than can be achieved in routine service delivery, may impede implementation of TAP, should it be demonstrated to exhibit positive clinical and cost-effectiveness outcomes. Therefore, the second part of the study proposes to evaluate the clinical and cost-effectiveness of TAP in regards to likely real-world delivery (i.e., after waiting 6 months for treatment) (TAP with wait).
The treatment access pathway (TAP) TAP utilises existing allied health and nursing staffing, within the context of a GP shared care model, to provide a multidisciplinary pain centre entry point for non-urgent patients that is not contingent on receipt of a Pain Specialist assessment. TAP is an allied health and nursing expanded scope of practice model of care with full-scope (first-contact, referring to other professionals, criteria-led discharge) and extended-scope (trans-disciplinary skill sharing assessment and discharge) clinics. Components of TAP in order are Pain Services Introduction, Choose your Path (group or individual assessment) and then a combination of group only, group and individual allied health or individual allied health only interventions depending on what the patient chooses. Further explanation of the interventions on offer are below:
Pain Service Introduction:
A 90-minute large group introduction to the IPPC including service aims and expectations; an introduction to pain physiology; and further information about IPPC treatment components. At the end of this session patients elect to continue with IPPC assessment and treatment, or can elect to self-discharge if they do not require the service.
Choose Your Path Assessment:
A 5 hour small group session to assess and identify areas that may be contributing to ongoing pain. Education provided from psychology, occupational therapy, physiotherapy, nursing and pharmacy on pain physiology, thoughts and emotions, daily activities, physical health, lifestyle and medications. A modified 90 minute session is available for patients unsuitable for a group setting due to hearing, vision, cognitive, emotional or language barriers. Patients are guided to develop an individual pain management plan that provides the basis for their treatment pathway through the IPPC.
Treatment interventions
Patients then complete a combination of multidisciplinary group and individual allied health treatments, tailored to their individual pain management plan established at the Choose Your Path group assessment.
PACE (Pain Activity Coping Education) - group:
An intensive multidisciplinary program involving 8 sessions run two days per week over 4 weeks (44 hours total). Includes education and practical sessions about understanding pain; movement (QiGong, aquatic physiotherapy, strength, stretch sessions), graded walking programs, activity pacing, managing daily activities, acceptance and commitment therapy, relaxation, mindfulness, healthy lifestyles, medication and community resources.
Bounce Back - group:
Specific to neck and back pain, this small group runs 2 hours per week for 4 weeks with both pre- and post-assessment sessions (10 hours total), and provides education on pain, anatomy, muscles and nerves of the back. Includes creation of walking and exercise programs, postures for daily activities, and managing flare ups.
Mindfulness - group:
2 hours per week for 6 weeks (12 hours total), this is a modified Mindfulness Stress Based Reduction Program. Introduces the principles and practices of mindfulness, as a strategy to cope with stress, pain, and improve quality of life.
Aquatic Physiotherapy - group:
1 hour per week for 4 weeks (4 hours total) to develop and practice an individual water-based movement program.
Individual allied health sessions:
• Psychology: Assessment and formulation of biological, psychological and social factors that predispose precipitate and perpetuate an individual’s experience of persistent pain. Treatment provided with the view to foster greater quality of life and improved mental health and well-being.
• Physiotherapy: Aims to improve quality of life by increasing level of activity and participation. Assessment and treatment can focus on pathology, movement patterns or function, with education and self-empowerment to facilitate active management of persistent pain.
• Occupational Therapy: Aims for people to participate in the activities of everyday life. Assessment focuses on the impact of pain on daily life and quality of life. Treatment provided to optimise occupational performance and engagement, develop self- efficacy and pain self-management skills.
• Pharmacy: Assessment of current and past medication, adherence and appropriateness. Education provided on safe and effective use of medications, appropriate medication-taking behaviours. Recommendations provided to optimise all treatment options including management of relevant concurrent disease processes, and review following commencement of new medication.
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Intervention code [1]
298645
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Treatment: Other
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Intervention code [2]
298691
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Rehabilitation
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Comparator / control treatment
Participants allocated to the waitlist control will remain on the waitlist for six months. Nil treatment will be provided by the IPPC during that time.
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Control group
Active
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Outcomes
Primary outcome [1]
302845
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BPI - Interference
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Assessment method [1]
302845
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Timepoint [1]
302845
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TAP treatment group: T1 (day 1) and T2 (6 months post day 1)
TAP with wait group : T1 (day 1), T2 (6 months post day 1) and T3 (12 months post day 1)
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Secondary outcome [1]
337227
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BPI - Pain scale
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Assessment method [1]
337227
0
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Timepoint [1]
337227
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TAP treatment group: T1 (day 1) and T2 (6 months post day 1) TAP with wait group : T1 (day 1), T2 (6 months post day 1)
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Secondary outcome [2]
337230
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DASS - Depression
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Assessment method [2]
337230
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Timepoint [2]
337230
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TAP treatment group: T1 (day 1) and T2 (6 months post day 1) TAP with wait group : T1 (day 1), T2 (6 months post day 1)
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Secondary outcome [3]
337232
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Patient Global Impression of Change
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Assessment method [3]
337232
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Timepoint [3]
337232
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TAP treatment group: T1 (day 1) and T2 (6 months post day 1) TAP with wait group : T1 (day 1), T2 (6 months post day 1)
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Secondary outcome [4]
337233
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NIH toolbox - Motor - 2MWT (2 minute walk test)
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Assessment method [4]
337233
0
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Timepoint [4]
337233
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TAP treatment group: T1 (day 1) and T2 (6 months post day 1) TAP with wait group : T1 (day 1), T2 (6 months post day 1)
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Secondary outcome [5]
337234
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CPAQ - Pain Willingness domain
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Assessment method [5]
337234
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Timepoint [5]
337234
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TAP treatment group: T1 (day 1) and T2 (6 months post day 1) TAP with wait group : T1 (day 1), T2 (6 months post day 1)
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Secondary outcome [6]
337235
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CPAQ - Activity Engagement domain
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Assessment method [6]
337235
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Timepoint [6]
337235
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TAP treatment group: T1 (day 1) and T2 (6 months post day 1) TAP with wait group : T1 (day 1), T2 (6 months post day 1)
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Secondary outcome [7]
337237
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DASS - Anxiety
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Assessment method [7]
337237
0
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Timepoint [7]
337237
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TAP treatment group: T1 (day 1) and T2 (6 months post day 1) TAP with wait group : T1 (day 1), T2 (6 months post day 1)
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Secondary outcome [8]
338346
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DASS -Stress
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Assessment method [8]
338346
0
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Timepoint [8]
338346
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TAP treatment group: T1 (day 1) and T2 (6 months post day 1) TAP with wait group : T1 (day 1), T2 (6 months post day 1)
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Secondary outcome [9]
338347
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Pain Self Efficacy Questionnaire (PSEQ)
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Assessment method [9]
338347
0
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Timepoint [9]
338347
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TAP treatment group: T1 (day 1) and T2 (6 months post day 1) TAP with wait group : T1 (day 1), T2 (6 months post day 1)
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Secondary outcome [10]
338348
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Pain Catastrophising Scale (PCS)
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Assessment method [10]
338348
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Timepoint [10]
338348
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TAP treatment group: T1 (day 1) and T2 (6 months post day 1) TAP with wait group : T1 (day 1), T2 (6 months post day 1)
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Secondary outcome [11]
338350
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Tampa Scale of Kinesiophobia (TSK)
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Assessment method [11]
338350
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Timepoint [11]
338350
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TAP treatment group: T1 (day 1) and T2 (6 months post day 1) TAP with wait group : T1 (day 1), T2 (6 months post day 1)
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Eligibility
Key inclusion criteria
Greater than or equal to 18 years of age;
Have experienced chronic non-cancer pain for more than 3 months;
Be proficient in written and spoken English;
Have a referral triaged as a category 3 (routine); and
Be deemed suitable for TAP by their GP.
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Minimum age
18
Years
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Maximum age
No limit
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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
Have a medical/psychiatric condition that would prevent TAP engagement;
Be scheduled for surgical or interventional treatment related to their pain condition within next 6 months;
Have been engaged with IPPC within the last 12 months.
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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)
Central randomisation by computer
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Permuted block randomisation
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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
Other
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Other design features
Study 1: TAP no wait group is parallel with waitlist
Study 2: One arm crossover - waitlist group crosses over and becomes TAP with wait group and receives treatment.
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
A-priori power analysis was completed to determine the necessary sample size N of the study, given a desired alpha level, a desired power level (1-B), and the size of the effect to be detected. The G*Power statistical package was used (Faul, F. 2007). Preliminary clinical data (unpublished) of the outcome measures shows a range of effect size between 0.3 (Depression) and 0.68 (Pain Acceptance).
Using a one tail t-test of independent groups at a significance level of p < 0.05 and a power of 80% with an effect size of 0.4 (moderate range) a sample size of N = 156 (78 in each group) will be required to reject the null hypothesis. If the groups are not of a normal distribution an increase in sample size of 28 (14 in each group) will be required. Attrition of 20% between commencement and 6 months is expected and will be accounted for with an additional 40 recruits (20 in each group) i.e. 196 participants will be recruited in total.. It is expected that 78 participants will be crossed over from waitlist to TAP (i.e., ‘TAP with wait’ group), and data for 78 participants will be available from the ‘TAP without wait’ group.
Data analyst will be masked to group allocation. Comparisons will be made between pre-post changes in outcomes for the two groups (i.e., ‘TAP without wait’ vs ‘TAP with wait’). Measures at 6 months will be analysed using a linear mixed model 45 (choice based on Akaike Information Criteria),46 with group, subjects and baseline measures as fixed factors, a random effect and covariate, respectively. SPSS (v22) will be used to analyse by intention to treat with two-tailed alpha set at 0.05. A t-test (alpha=0.05) will be used to test whether mean pre-post changes in outcome variables are different between groups (i.e., TAP without wait’ vs ‘TAP with wait’).
A t-test of independent groups will be used to examine whether the mean TAP costs/QALY gained is significantly different to $73,000 (inflation adjusted value).
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
11/09/2017
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Actual
11/09/2017
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Date of last participant enrolment
Anticipated
25/06/2018
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Actual
3/05/2019
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Date of last data collection
Anticipated
8/05/2020
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Actual
8/05/2020
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Sample size
Target
196
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Accrual to date
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Final
181
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Recruitment in Australia
Recruitment state(s)
QLD
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Recruitment hospital [1]
8587
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Gold Coast University Hospital - Southport
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Recruitment postcode(s) [1]
16694
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4215 - Southport
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Funding & Sponsors
Funding source category [1]
297031
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Government body
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Name [1]
297031
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Health Practitioner Research Scheme, Queensland Health
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Address [1]
297031
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Allied Health Professions’ Office of Queensland, Clinical Excellence Division
Department of Health
Level 1, 15 Butterfield Street,
Herston, QLD 4006
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Country [1]
297031
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Australia
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Funding source category [2]
297414
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Hospital
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Name [2]
297414
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Gold Coast Hospital and Health Service
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Address [2]
297414
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1 Hospital Blvd, Southport QLD 4215
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Country [2]
297414
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Australia
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Primary sponsor type
Individual
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Name
Margaret Vandermost
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Address
Interdisciplinary Persistent Pain Centre
2 Investigator Drive, Robina, Queensland 4226
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Country
Australia
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Secondary sponsor category [1]
296033
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Hospital
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Name [1]
296033
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Interdisciplinary Persistent Pain Centre
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Address [1]
296033
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2 Investigator Drive, Robina, Queensland4226
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Country [1]
296033
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Australia
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Other collaborator category [1]
279695
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Individual
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Name [1]
279695
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Prof Michele Sterling
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Address [1]
279695
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Griffith University
School of Allied Health,
Menzies Health Institute
Parklands Drive
SOUTHPORT QLD 4222
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Country [1]
279695
0
Australia
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Other collaborator category [2]
279696
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Individual
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Name [2]
279696
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Karl Bagraith
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Address [2]
279696
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Interdisciplinary Persistent Pain Centre
2 Investigator Drive, Robina, Queensland 4226
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Country [2]
279696
0
Australia
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Other collaborator category [3]
279697
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Individual
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Name [3]
279697
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Hannah Kennedy
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Address [3]
279697
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Interdisciplinary Persistent Pain Centre
2 Investigator Drive, Queensland 4226
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Country [3]
279697
0
Australia
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Other collaborator category [4]
279698
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Individual
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Name [4]
279698
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Darren Doherty
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Address [4]
279698
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Interdisciplinary Persistent Pain Centre
2 Investigator Drive, Robina Queensland 4226
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Country [4]
279698
0
Australia
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Other collaborator category [5]
279699
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Individual
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Name [5]
279699
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Simon Kilner
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Address [5]
279699
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Interdisciplinary Persistent Pain Centre
2 Investigator Drive, Robina, Queensland 4226
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Country [5]
279699
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Australia
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Other collaborator category [6]
281249
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Individual
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Name [6]
281249
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Associate Professor - Biostatistician Mark Jones
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Address [6]
281249
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Institute for Evidence-Based Healthcare, Faculty of Health Sciences & Medicine, Level 4, Building 5, Faculty of Health Sciences & Medicine, Bond University, 14 University Drive, Robina QLD 4226
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Country [6]
281249
0
Australia
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Other collaborator category [7]
281250
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Individual
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Name [7]
281250
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Professor David Henry
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Address [7]
281250
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Professor of Evidence-Based Practice, Institute for Evidence-Based Healthcare Faculty of Health Sciences & Medicine,
Level 4, Building 5, Faculty of Health Sciences & Medicine, Bond University, 14 University Drive, Robina QLD 4226
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Country [7]
281250
0
Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
298216
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Gold Coast Hospital and Health Service Human Research Ethics Committee (EC00160)
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Ethics committee address [1]
298216
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Research Directorate Level 2, Pathology and Education Building 1 Hospital Boulevard Southport QLD 4215
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Ethics committee country [1]
298216
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Australia
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Date submitted for ethics approval [1]
298216
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25/05/2016
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Approval date [1]
298216
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19/10/2016
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Ethics approval number [1]
298216
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HREC/16/QGC/156
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Summary
Brief summary
The first part of the study aims to investigate whether an innovative allied health expanded scope Treatment Access Pathway (TAP) improves health outcomes compared to a waitlist control. The second part of the study (crossover) will investigate the clinical effectiveness of TAP following 6 months waiting for treatment. Measures of health outcomes will be objective measures of function and patient self-reports of physical function, pain, mood, acceptance, self-efficacy and health related quality of life. A secondary aim of the project is to investigate the cost-effectiveness of TAP utilising a cost-utility ratio, based on delivery cost/quality adjusted life years. We anticipate 196 participants referred to the Gold Coast Interdisciplinary Persistent Pain Centre (IPPC) will be recruited into the study. Participants will be included if they are over 18 years of age, have non-cancer pain of greater than 3 months duration, and able to read and write adequate English to complete questionnaires. Data will be collected from participants from two cohorts: 1) those receiving standard treatment through TAP (treatment) and 2) those on the waitlist (control). As part of routine practice, all IPPC patients receiving treatment complete objective measures and a battery of self-report questionnaires about their health-related quality of life at regular time points. Both the waitlist and treatment groups will complete the questionnaires following referral to the service (time 1) and at 6 months post referral (time 2). Additionally, the waitlist group (who will crossover into the “TAP with wait” treatment group at 6 months post referral) will complete the questionnaires at 12 months post referral (time 3). Study 1 Primary Hypothesis: Treatment Access Pathway (TAP) patients at six months will have clinically important changes in objective physical function and self-report outcome measures (pain, mood, acceptance, self-efficacy, catastrophising and HRQOL) compared with waitlist patients. Secondary Hypothesis: The TAP delivery cost/quality adjusted life year gained will be less than $73,000/QALY 21,23. Study 2 Primary Hypothesis: There is no significant difference in clinical outcomes (changes in pain, objective physical function, mood, acceptance, self-efficacy, and HRQOL) between patients that wait (6 months) and do not wait for TAP. Secondary Hypothesis: There is no significant difference in cost-effectiveness (TAP delivery cost/quality adjusted life year gained) between patients that wait (6 months) and do not wait for TAP.
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Trial website
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Trial related presentations / publications
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Public notes
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Attachments [1]
1904
1904
0
0
/AnzctrAttachments/373328-HREC 16 QGC 156 AM01 approval, dated 31.03.2017.pdf
(Ethics approval)
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Attachments [2]
1905
1905
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0
/AnzctrAttachments/373328-Authorisation 16 160, dated 23.02.2017.pdf
(Ethics approval)
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Contacts
Principal investigator
Name
76370
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Mrs Margaret Vandermost
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Address
76370
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Interdisciplinary Persistent Pain Centre
2 Investigator Drive, Robina Queensland 4226
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Country
76370
0
Australia
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Phone
76370
0
+617 5668 6825
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Fax
76370
0
+617 5680 9539
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Email
76370
0
[email protected]
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Contact person for public queries
Name
76371
0
Hannah Kennedy
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Address
76371
0
Interdisciplinary Persistent Pain Centre
2 Investigator Drive, Robina Queensland 4226
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Country
76371
0
Australia
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Phone
76371
0
+617 5668 6825
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Fax
76371
0
+617 5680 9539
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Email
76371
0
[email protected]
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Contact person for scientific queries
Name
76372
0
Margaret Vandermost
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Address
76372
0
Interdisciplinary Persistent Pain Centre
2 Investigator Drive, Robina Queensland 4226
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Country
76372
0
Australia
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Phone
76372
0
+617 5668 6825
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Fax
76372
0
+617 5680 9539
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Email
76372
0
[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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What supporting documents are/will be available?
No Supporting Document Provided
Doc. No.
Type
Citation
Link
Email
Other Details
Attachment
5675
Study protocol
373328-(Uploaded-04-11-2019-16-06-25)-Study-related document.docx
5676
Ethical approval
373328-(Uploaded-04-11-2019-16-07-06)-Study-related document.pdf
7413
Statistical analysis plan
373328-(Uploaded-03-03-2020-09-01-03)-Study-related document.docx
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Embase
Improvement in pain interference and function by an allied health pain management program: Results of a randomized trial.
2021
https://dx.doi.org/10.1002/ejp.1836
N.B. These documents automatically identified may not have been verified by the study sponsor.
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