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Trial registered on ANZCTR
Registration number
ACTRN12623000213640
Ethics application status
Approved
Date submitted
16/02/2023
Date registered
28/02/2023
Date last updated
11/08/2024
Date data sharing statement initially provided
28/02/2023
Type of registration
Prospectively registered
Titles & IDs
Public title
Exploring the efficacy of remote stepped care treatment for obsessive-compulsive disorder: A feasibility study.
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Scientific title
Exploring the efficacy of remote stepped care treatment for obsessive-compulsive disorder in adults: A feasibility study.
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Secondary ID [1]
309008
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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:
obsessive compulsive disorder
329050
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Condition category
Condition code
Mental Health
326031
326031
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0
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Anxiety
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Mental Health
326032
326032
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0
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Other mental health disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
In Step 1 of this stepped care treatment all participants will read a self-help book 'Stop Obsessing: How to Overcome Your Obsessions and Compulsions' by Edna Foa and Reid Wilson, which will be sent to them in the mail over an 8 week period, along with a suggested reading schedule. During these 8 weeks participants also receive weekly email support from a provisional psychologist or psychologist to answer any questions as they work through the book. Adherence to the readings will be monitored in the weekly emails to participants. We estimate that participants will spend approximately 1 hour per week reading the book and working on the skills.
After completing Step 1, participants symptoms of obsessive-compulsive disorder (OCD) will be re-assessed. Participants whose symptoms of OCD do not improve according to the response criteria (Yale Brown Obsessive Compulsive Scale (YBOCS) reduction of greater than or equal to 25% and a Clinical Global Impression Improvement Scale (CGI-I) score of less than or equal to 3) will go onto receive Step 2 of the remote stepped care treatment.
Step 2 of the stepped-care treatment consists of individually delivered internet-videoconferencing delivered CBT [(VCBT); 8 weekly 50-minute sessions)]. The VCBT will be manualised and will focus on the construction of an exposure hierarchy and graded exposure exercises to items on the exposure hierarchy, combined with refraining of engaging in compulsive behaviours (participants will be asked to cease their compulsions). Exposure hierarchy items will be individualised for each participant and may include items related to contamination/washing, responsibility/checking, unacceptable thoughts/mental rituals or symmetry obsessions/compulsions. The VCBT treatment will be provided by a provisional psychologist or psychologist with experience ranging from 1-5 years. Adherence to the treatment will be monitored by the clinician each week.
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Intervention code [1]
325450
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Behaviour
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Intervention code [2]
325451
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Treatment: Other
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Comparator / control treatment
This is an open trial. There is no control group.
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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OCD symptom severity assessed using the Yale Brown Obsessive Compulsive Scale
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Assessment method [1]
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Timepoint [1]
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Pre-treatment
Weekly in step 1
Mid-treatment (week 5 of step 1)
Post step 1 (week 9 post-commencement of intervention)
Weekly in step 2
Post step 2 (week 17 post-commencement of intervention; primary endpoint)
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Primary outcome [2]
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OCD symptom severity assessed using the Dimensional Obsessive Compulsive Scale
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Assessment method [2]
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Timepoint [2]
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Pre-treatment
Mid-treatment (week 5 of step 1)
Post step 1 (week 9 post-commencement of intervention)
Post step 2 (week 17 post-commencement of intervention; primary endpoint)
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Primary outcome [3]
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Acceptability will be measured with the Client Satisfaction Questionnaire
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Assessment method [3]
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Timepoint [3]
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Post step 1 (week 9 post-commencement of intervention)
Post step 2 (week 17 post-commencement of intervention; primary endpoint)
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Secondary outcome [1]
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Depressive symptom severity assessed using the Patient Health Questionnaire - 9 item
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Assessment method [1]
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Timepoint [1]
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Pre-treatment
Weekly in step 1
Mid-treatment (week 5 of step 1)
Post step 1 (week 9 post-commencement of intervention)
Weekly in step 2
Post step 2 (week 17 post-commencement of intervention)
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Secondary outcome [2]
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OCD symptom severity assessed using the Clinical Global Impression Scale - Severity
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Assessment method [2]
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Timepoint [2]
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Pre-treatment
Mid-treatment (week 5 of step 1)
Post step 1 (week 9 post-commencement of intervention)
Post step 2 (week 17 post-commencement of intervention)
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Secondary outcome [3]
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OCD symptom improvement assessed using the Clinical Global Impression Scale - Improvement Scale
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Assessment method [3]
418635
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Timepoint [3]
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Mid-treatment (week 5 of step 1)
Post step 1 (week 9 post-commencement of intervention)
Post step 2 (week 17 post-commencement of intervention)
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Secondary outcome [4]
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Obsessive Beliefs Questionnaire
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Assessment method [4]
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Timepoint [4]
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Pre-treatment
Mid-treatment (week 5 of step 1)
Post step 1 (week 9 post-commencement of intervention)
Post step 2 (week 17 post-commencement of intervention)
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Secondary outcome [5]
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Core Beliefs Questionnaire
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Assessment method [5]
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Timepoint [5]
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Pre-treatment
Mid-treatment (week 5 of step 1)
Post step 1 (week 9 post-commencement of intervention)
Post step 2 (week 17 post-commencement of intervention)
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Secondary outcome [6]
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Feasibility will be assessed by monitoring participant dropout rates through file audit.
This is an additional primary outcome
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Assessment method [6]
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Timepoint [6]
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Post step 1 (week 9 post-commencement of intervention)
Post step 2 (week 17 post-commencement of intervention; primary endpoint)
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Eligibility
Key inclusion criteria
(a) English speaking;
(b) Australian resident;
(c) 18 years-of-age or above;
(d) Have regular access to the internet;
(e) No suicidal plans or intention, or recent history of suicide attempts or deliberate self-harm;
(f) A score of at least 16 on the Yale-Brown Obsessive Compulsive Scale (YBOCS);
(g) A score of at least 7 on the Dimensional Obsessive Compulsive Scale (DOCS);
(h) Meet criteria for OCD as primary on the Diagnostic Interview for Anxiety, Mood, Obsessive-Compulsive and other Neuropsychiatric Disorders (DIAMOND).
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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
None
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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)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
1/03/2023
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Actual
31/05/2023
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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
14
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Final
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Recruitment in Australia
Recruitment state(s)
ACT,NSW,NT,QLD,SA,TAS,WA,VIC
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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University of Technology Sydney
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Address [1]
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Discipline of Clinical Psychology. Graduate School of Health. PO Box 123. Broadway. NSW 2007.
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Country [1]
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Australia
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Primary sponsor type
University
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Name
University of Technology Sydney
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Address
Discipline of Clinical Psychology. Graduate School of Health. PO Box 123. Broadway. NSW 2007.
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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]
314942
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Country [1]
314942
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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University of Technology Sydney Human Research Ethics Committee
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Ethics committee address [1]
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University of Technology Sydney, Ultimo, NSW, 2007
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
312451
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Approval date [1]
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15/02/2023
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Ethics approval number [1]
312451
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Summary
Brief summary
The purpose of this project is to assess the acceptability and feasibility of a remote stepped care treatment for individuals with obsessive-compulsive disorder. After assessment all participants will commence clinician-guided cognitive-behavioural bibliotherapy (BCBT) for 8 weeks. Participants who do not meet the predefined response criteria (YBOCS reduction of greater than or equal to 25% and a CGI-I score of less than or equal to 3) will then complete 8 sessions of internet-videoconferencing cognitive-behavioural therapy (VCBT) with a psychologist.
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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 Bethany Wootton
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Address
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Discipline of Clinical Psychology. Graduate School of Health.University of Technology Sydney
PO Box 123. Broadway. NSW 2007
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Country
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Australia
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Phone
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+61 2 9514 3942
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Fax
124714
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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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Bethany Wootton
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Address
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Discipline of Clinical Psychology. Graduate School of Health.University of Technology Sydney
PO Box 123. Broadway. NSW 2007
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Country
124715
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Australia
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Phone
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+61 2 9514 3942
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Fax
124715
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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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Bethany Wootton
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Address
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Discipline of Clinical Psychology. Graduate School of Health.University of Technology Sydney
PO Box 123. Broadway. NSW 2007
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Country
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Australia
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Phone
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+61 2 9514 3942
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Fax
124716
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Email
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
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What data in particular will be shared?
Non-identifiable individual participant data of published results for primary outcome measures.
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When will data be available (start and end dates)?
At the completion of the study and after all relevant manuscripts are published for a period of 5 years.
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Available to whom?
Any academic who has expertise in the field of obsessive compulsive disorder
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Available for what types of analyses?
Any
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How or where can data be obtained?
From the Chief Investigator (
[email protected]
)
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What supporting documents are/will be available?
No Supporting Document Provided
Doc. No.
Type
Citation
Link
Email
Other Details
Attachment
18362
Study protocol
Study protocol
385414-(Uploaded-16-02-2023-15-35-20)-Study-related document.doc
18363
Informed consent form
Participant Information Sheet and Consent Form
385414-(Uploaded-16-02-2023-15-35-34)-Study-related document.doc
18364
Ethical approval
Ethical approval letter
385414-(Uploaded-16-02-2023-15-35-48)-Study-related document.pdf
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.
Download to PDF