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Trial registered on ANZCTR
Registration number
ACTRN12611000151932
Ethics application status
Approved
Date submitted
11/01/2011
Date registered
9/02/2011
Date last updated
10/08/2012
Type of registration
Prospectively registered
Titles & IDs
Public title
An open pilot trial of an Internet-based clinician-guided Cognitive Behavioural Therapy (CBT) plus Eye Movement Desensitization and Reprocessing (EMDR) program for Posttraumatic Stress Disorder (PTSD)
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Scientific title
An open trial of the effects of Cognitive Behavioural Therapy (CBT) plus Eye Movement Desensitization and Reprocessing (EMDR) on symptoms of Posttraumatic Stress Disorder (PTSD) using an Internet-based education program for PTSD.
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Secondary ID [1]
253385
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Nil
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Universal Trial Number (UTN)
Nil
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Trial acronym
Nil
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Posttraumatic stress disorder
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Condition category
Condition code
Mental Health
259069
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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
Participants will be assigned to a treatment group whereby they will complete 6 lessons of Internet based treatment about management of symptoms of posttraumatic stress disorder (PTSD). One lesson will be completed every 7 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 PTSD, taking a further 20 minutes per summary. From week 2 in the program they will receive instructions on using eye movement desensitzation and reprocessing (EMDR) and will be encouraged to use EMDR twice weekly until the end of the program for up to 45 minutes each session of EMDR. All participants will also receive automatic email and weekly reminder phone calls by a clinical psychologist. The duration of the reminder emails/phone calls and contribution to the forum is expected to be 5-10 minutes per week. The duration of the program is 6 weeks, but participants will be contacted 3 months post program and asked to complete follow-up questionnaires. All participants will have symptoms of PTSD but do not need to meet Diagnostic and Statistical Manual of Mental Disorders 4th Edition (DSM-IV) criteria for PTSD. Study questionnaires will be administered at application, pre-education, post-education, and at 3-months post-education. These will take about 20-30 minutes to complete. The treatment materials are based on the Anxiety and PTSD Programs, which apply cognitive behavioural techniques.
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Intervention code [1]
257832
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Treatment: Other
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Comparator / control treatment
Not applicable.
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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PTSD is measured by the PTSD Checklist - Civilian version (PCL-C)
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Assessment method [1]
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Timepoint [1]
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Administered at 3 days pre-treatment, one day post-treatment, and at 3-months post-treatment
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Secondary outcome [1]
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Neuroticism is measured by using the NEO-Five Factor Inventory (NEO-FFI) Neuroticism scale
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Assessment method [1]
268829
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Timepoint [1]
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Administered at 3 days pre-treatment, one day post-treatment, and at 3-months post-treatment
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Secondary outcome [2]
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Disability is measured by the Sheehan Disability Scale (SDS)
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Assessment method [2]
268830
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Timepoint [2]
268830
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Administered at 3 days pre-treatment, one day post-treatment, and at 3-months post-treatment
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Secondary outcome [3]
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Psychological distress is measured by the Kessler 10-item scale (K-10)
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Assessment method [3]
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Timepoint [3]
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Administered at 3 days pre-treatment, one day post-treatment, and at 3-months post-treatment
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Secondary outcome [4]
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Symptoms and severity of depression is measured by the Patient Health Questionnaire-9 (PHQ-9)
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Assessment method [4]
268832
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Timepoint [4]
268832
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Administered at 3 days pre-treatment, one day post-treatment, and at 3-months post-treatment
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Secondary outcome [5]
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Anxiety is measured by the Generalised Anxiety Disorder 7 Item Scale (GAD-7)
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Assessment method [5]
268833
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Timepoint [5]
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Administered at 3 days pre-treatment, one day post-treatment, and at 3-months post-treatment
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Eligibility
Key inclusion criteria
- PTSD symptoms above a recommended clinical cutoff - Internet access + printer access - Australian resident - Males and females
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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
- Psychotic disorder - Current or planned psychological treatment during study duration - Change in medications during last 1 month or intended change during study duration - Actively suicidal - Highly dissociative
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Study design
Purpose of the study
Educational / counselling / training
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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 apply online, followed by a telephone interview to confirm diagnosis via structured diagnostic interview using the Mini Neuropsychiatric Interview Schedule (MINI 5.0.0).
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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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
Completed
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Date of first participant enrolment
Anticipated
4/07/2011
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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
15
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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]
258302
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Charities/Societies/Foundations
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Name [1]
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New South Wales Institute for Psychiatry
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Address [1]
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Cumberland Hospital
5 Fleet Street, North Parramatta, NSW, 2151
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Country [1]
258302
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Australia
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Primary sponsor type
University
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Name
eCentreClinic
Centre for Emotional Health, Macquarie University
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Address
Macquarie University, Ryde, NSW, 2019
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
257466
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Country [1]
257466
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
260286
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Macquarie University of New South Wales Human Research Committee
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Ethics committee address [1]
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E11A, Macquarie University NSW 2109
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Ethics committee country [1]
260286
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Australia
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Date submitted for ethics approval [1]
260286
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Approval date [1]
260286
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06/01/2011
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Ethics approval number [1]
260286
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5201100382
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Summary
Brief summary
The purpose of this project is to explore whether a clinician-guided treatment program can help to reduce PTSD symptoms in a population of adults (aged 18-75), when administered over the internet. A secondary purpose is to determine how acceptable people find this form of treatment. The study will inform how services can best improve future treatment programs for adults with PTSD.
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Trial website
www.ecentreclinic.org
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Trial related presentations / publications
- Andrews, G. and N. Titov, Alternate models of care. Treating people you never see: Internet-based treatment of the internalizing mental disorders. Australian Health Review, In Press.
- Titov, N., et al., The Shyness Program: Longer Term Benefits, Cost-Effectiveness, and Acceptability. Australian & New Zealand Journal of Psychiatry, 2009. 43(1): p. 36-44.
- Titov, N, G. Andrews, and P.M. McEvoy, Key components in low intensity interventions for anxiety. Oxford Guide, submitted
- Titov, N. & G. Andrews, Email and brief internet based mental health interventions. Oxford Guide, submitted.
- Titov, N., et al., Brief Internet Treatment for Social Phobia reduces Comorbidity Australian and New Zealand Journal of Psychiatry in press.
- Titov N, Andrews G, Schwencke G: Shyness 2: Treating social phobia online: replication and extension. Australian and New Zealand Journal of Psychiatry 2008 42(7):595-605.
- Titov N, Andrews G, Schwencke G, Drobny J, Einstein D: Shyness 1: Distance treatment for social over the Internet. A randomized controlled trial. Australian & New Zealand Journal of Psychiatry 2008; 42(7):585-594.
- Titov N, Andrews G, Choi I, Schwencke G, Mahoney A: Shyness 3: An RCT of guided vs unguided internet based CBT for social phobia. Australian & New Zealand Journal of Psychiatry 2008; 42(12):1030-1040.
- Titov N. Status of computerized cognitive behavioural therapy for adults. Australian & New Zealand Journal of Psychiatry 2007; 41(2):95-114.
- Titov N, Andrews G, Robinson E, Schwencke G, Johnston L, Solley K, Choi I. Clinician-assisted internet treatment is effective for generalized anxiety disorder: randomized controlled trial. Australian and New Zealand Journal of Psychiatry 2009, 43:10, 905-912.
- Titov, N., Dear, B. F., Schwencke, G., Andrews, G., Johnston, L., Craske, M., & McEvoy, P. (submitted). Transdiagnostic internet treatment for anxiety and depression:
A randomised controlled trial. Behaviour Research and Therapy.
- Wims E, Titov N, Andrews G: The Climate Panic program: an open trial of Internet-based treatment for panic disorder. Electronic Journal of Applied Psychology 2008; 4(2)
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Dr Nickolai Titov
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Address
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Centre for Emotional Health, Macquarie University, Ryde, NSW, 2019
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Country
15326
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Australia
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Phone
15326
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+612 9850 9901
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Fax
15326
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+612 9850 8062
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Email
15326
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[email protected]
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Contact person for scientific queries
Name
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Dr Nickolai Titov
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Address
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Centre for Emotional Health, Macquarie University, Ryde, NSW, 2019
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Country
6254
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Australia
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Phone
6254
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+612 9850 9901
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Fax
6254
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+612 9850 8062
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Email
6254
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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
Source
Title
Year of Publication
DOI
Dimensions AI
Internet-delivered eye movement desensitization and reprocessing (iEMDR): an open trial
2013
https://doi.org/10.12688/f1000research.2-79.v2
N.B. These documents automatically identified may not have been verified by the study sponsor.
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