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Trial registered on ANZCTR
Registration number
ACTRN12614000146695
Ethics application status
Approved
Date submitted
31/01/2014
Date registered
5/02/2014
Date last updated
5/02/2014
Type of registration
Prospectively registered
Titles & IDs
Public title
A feasibility study examining the effectiveness and acceptability of an internet-delivered education program, The Pain Course, for chronic pain patients with anxiety and depression in a tertiary pain service.
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Scientific title
A feasibility study examining the effectiveness and acceptability of an internet-delivered education program, The Pain Course, for chronic pain patients with anxiety and depression in a tertiary pain service.
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Secondary ID [1]
284011
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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:
Chronic Pain
291044
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Anxiety
291087
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Depression
291088
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Condition category
Condition code
Anaesthesiology
291384
291384
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0
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Pain management
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Mental Health
291385
291385
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0
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Depression
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Mental Health
291386
291386
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0
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Anxiety
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
All participants will complete 5 lessons of an internet-delivered cognitive behaviour therapy (iCBT) treatment, the Pain Course (Dear et al., 2013) focusing on the management of pain, anxiety, depression and disability. All 5 Lessons will be administered online (via the internet) and one lesson will be completed every 7 to 10 days. Each lesson will take about 15 minutes to complete. Participants will also have access to summaries of each lesson, and will read anonymous stories about other people with chronic pain, taking a further 20 minutes per summary. All participants will also receive weekly reminder emails and weekly phone calls by a clinical psychologist. The duration of the reminder emails and phone calls is expected to be 5-10 minutes per week. The duration of the program is 8 weeks. Study questionnaires will be administered at application, pre-treatment, during the treatment, post-treatment, and 3 months post-treatment. These questionnaires at application, pre-treatment, post-treatment and 3-months follow up will take about 10 minutes to complete. The questionnaires administered during the treatment will take approximately 2 minutes to complete. The software presenting the iCBT treatment course will also record information to inform adherence to the intervention (e.g. lessons completed, download history of other treatment materials in the course, number of logins, and duration of logins).
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Intervention code [1]
288694
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Treatment: Other
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Intervention code [2]
288727
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Behaviour
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Comparator / control treatment
N/A - This is a single group study.
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Patient Health Questionnaire 9-Item (PHQ9), which is a measure of depression.
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Assessment method [1]
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Timepoint [1]
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Application; pre-treatment; once per week throughout treatment; post-treatment, and; 3 month follow-up
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Primary outcome [2]
291375
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Generalized Anxiety Disorder 7-Item (GAD7), which is a measure of anxiety.
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Assessment method [2]
291375
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Timepoint [2]
291375
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Pre-treatment; once per week throughout treatment; post-treatment, and; 3 month follow-up
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Primary outcome [3]
291376
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Roland Morris Disability Questionnaire (RMDQ), which measures disability associated with pain.
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Assessment method [3]
291376
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Timepoint [3]
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Pre-treatment; post-treatment, and; 3 month follow-up
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Secondary outcome [1]
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Wisconsin Brief Pain Questionnaire (WBPQ), which is a general measure of the nature of participants pain including location, severity and duration.
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Assessment method [1]
306622
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Timepoint [1]
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Pre-treatment; post-treatment, and; 3 month follow-up
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Secondary outcome [2]
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Pain Self-Efficacy Questionnaire (PSEQ) which is a measure of self-rated pain-related self-efficacy beliefs.
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Assessment method [2]
306623
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Timepoint [2]
306623
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Pre-treatment; post-treatment, and; 3 month follow-up
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Secondary outcome [3]
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Tampa Scale of Kinesiophobia (TSK), which is a measure of fear of movement and re-injury.
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Assessment method [3]
306624
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Timepoint [3]
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Pre-treatment; post-treatment, and; 3 month follow-up
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Eligibility
Key inclusion criteria
- Has experienced Chronic Pain (i.e. Pain > 3 months)
- Self-reported difficulties with anxiety or depression.
- Internet access + Printer access
- Australian resident
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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
- Receiving concurrent CBT
- Severe symptoms of depression
- Severe depression, suicidal intent or plan (PHQ-9 total score > 23; or >2 to PHQ-9 question assessing frequency of self-harm or suicide ideation)
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Participants will be patients receiving treatment for chronic pain at the Pain Management Unit at Prince of Wales Hospital. Patients will be informed of the study by an invitation letter and the Participant Information Sheet delivered in person or by mail by nursing staff unrelated to the study. Participants returning consent forms will be contacted by a Clinical Psychologist in person or by phone at a time convenient to the participant to administer the PHQ-9 and a brief telephone interview to confirm the program is suitable for applicants.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
N/A. This is an open trial design.
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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
Single group
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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
Not yet recruiting
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Date of first participant enrolment
Anticipated
10/02/2014
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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)
NSW
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Recruitment hospital [1]
2024
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Prince of Wales Private Hospital - Randwick
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Funding & Sponsors
Funding source category [1]
288631
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Hospital
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Name [1]
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Pain Management Unit, Prince of Wales Hospital
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Address [1]
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Barker St, Randwick NSW 2031
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Country [1]
288631
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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
eCentreClinic, The Centre For Emotional Health (CEH), Department of Psychology, Macquarie University, NSW, 2109, Australia.
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Country
Australia
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Secondary sponsor category [1]
287338
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None
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Name [1]
287338
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Address [1]
287338
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Country [1]
287338
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Other collaborator category [1]
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Individual
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Name [1]
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Ms Catherine Courtney
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Address [1]
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Pain Management Unit, Prince of Wales Hospital, Barker St, Randwick, NSW, 2031
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Country [1]
277791
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Australia
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Other collaborator category [2]
277792
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Individual
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Name [2]
277792
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Dr Blake Dear
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Address [2]
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Department of Psychology, Macquarie University, NSW, 2109
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Country [2]
277792
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Australia
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Other collaborator category [3]
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Individual
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Name [3]
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Dr Luke James Johnston
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Address [3]
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Department of Psychology, Macquarie University, NSW, 2109
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Country [3]
277793
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Australia
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Other collaborator category [4]
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Individual
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Name [4]
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Professor Nickolai Titov
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Address [4]
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Department of Psychology, Macquarie University, NSW, 2109
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Country [4]
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Australia
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Other collaborator category [5]
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Individual
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Name [5]
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Dr Kok Eng Khor
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Address [5]
277795
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Pain Management Unit, Prince of Wales Hospital, Barker St, Randwick, NSW, 2031
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Country [5]
277795
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
290488
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NSW Health South Eastern Sydney Local Health District Human Research Ethics Committee
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Ethics committee address [1]
290488
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Room G71 East Wing Edmund Blacket Building Prince of Wales Hospital Randwick NSW 2031
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Ethics committee country [1]
290488
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Australia
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Date submitted for ethics approval [1]
290488
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Approval date [1]
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06/11/2013
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Ethics approval number [1]
290488
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13/175
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Summary
Brief summary
This project builds on an earlier projects and seeks to examine the efficacy and acceptability of the Pain Course when provided in a tertiary pain service. We expect that participants will report improvements in symptoms of anxiety, depression and disability levels.
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Trial website
www.ecentreclinic.org
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Trial related presentations / publications
- Dear, BF., Titov, N., Perry, KN., Johnston, L., Wootton, B., Terides, M., Rapee, R., Hudson, J. (2013). The Pain Course: A randomised controlled trial of clinician-guided internet-delivered cognitive behaviour therapy program for managing chronic pain and emotional wellbeing. Pain, 154, 942-950. - Dear, B. F., Titov, N., Schwencke, G., Andews, G., Johnston, L., Craske, M. G., & McEvoy, P. (2011). An open trial of a brief transdiagnostic treatment for anxiety and depression. Behaviour Research and Therapy, 49, 830-837. - Johnston, L., Titov, N., Andrews, G., Spence, J., & Dear, B.F. (2011). A RCT of a transdiagnostic internet-delivered treatment for three anxiety disorders: Examination of support roles and disorder-specific outcomes. PLoS ONE 6(11): e28079. - Titov N., Dear B.F., Schwencke G., Andrews G., Johnston L., Craske M., & McEvoy, P. (2011). Transdiagnostic Internet treatment of anxiety and depression: A randomised controlled trial. Behaviour Research and Therapy, 49, 441-452. - Titov, N., Andrews, G., Johnston, L., Robinson, E., & Spence, J. (2010). Transdiagnostic Internet treatment for anxiety disorders: A randomized controlled trial. Behaviour Research and Therapy, 48, 890-899.
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Public notes
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Contacts
Principal investigator
Name
45930
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Ms Catherine Courtney
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Address
45930
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Pain Management Unit, Prince of Wales Hospital, Barker St, Randwick, NSW 2031
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Country
45930
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Australia
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Phone
45930
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61 2 9382 2958
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Fax
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Email
45930
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[email protected]
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Contact person for public queries
Name
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Catherine Courtney
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Address
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Pain Management Unit, Prince of Wales Hospital, Barker St, Randwick, NSW 2031
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Country
45931
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Australia
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Phone
45931
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61 2 9382 2958
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Fax
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Email
45931
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[email protected]
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Contact person for scientific queries
Name
45932
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Blake Dear
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Address
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eCentreClinic, The Centre for Emotional Health, Department of Psychology, Macquarie University, NSW, 2109.
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Country
45932
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Australia
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Phone
45932
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61 2 9850 9979
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Fax
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Email
45932
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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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