Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12617000825358
Ethics application status
Approved
Date submitted
18/05/2017
Date registered
6/06/2017
Date last updated
18/07/2024
Date data sharing statement initially provided
6/05/2019
Date results provided
19/06/2024
Type of registration
Prospectively registered

Titles & IDs
Public title
The cannabidiol youth anxiety pilot study (CAPS): a 12-week open- label pilot study of cannabidiol for anxiety disorders
Scientific title
The cannabidiol youth anxiety pilot study (CAPS): a 12-week open- label pilot study of the safety, tolerability and efficacy of cannabidiol for anxiety disorders
Secondary ID [1] 291931 0
Nil known.
Universal Trial Number (UTN)
Trial acronym
CAPS
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Anxiety 303295 0
Condition category
Condition code
Mental Health 302723 302723 0 0
Anxiety

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Experimental intervention: All participants will receive open-label cannabidiol (CBD) for 12 weeks.
Background intervention: All participants will be offered biweekly cognitive-behaviour therapy (CBT) for 12 weeks (5 sessions). CBT will be administered as one-on-one sessions (1hr) by a qualified clinician at the study site (one of four headspace centres).

CBD will be administered on a fixed–flexible schedule beginning with 200 mg (oral capsule) per day and adjusted up to 800 mg per day by week 8. Until week 8, participants who are considered to have failed to improve using the CGI-I (operationalised as a score of >=3) and who are tolerating the medication are eligible for dose increases at each assessment. Dose escalation can occur with 200 mg/day increments, with at least a 4-week gap between dose increments, except for the first dose increase (200mg/day to 400mg/day), which can occur at the end of week 1 after tolerance of the initial dose of the study medication has been established. Participants who receive 400mg/day after week 1 are also eligible for the next dose increase at week 4. Adherence to the trial medication will be assessed by pill count.
Intervention code [1] 298073 0
Treatment: Drugs
Intervention code [2] 298074 0
Treatment: Other
Comparator / control treatment
No control group.
Control group
Uncontrolled

Outcomes
Primary outcome [1] 302118 0
Anxiety severity after 12 weeks, measured on the Overall Anxiety Severity and Impairment Scale (OASIS). Total scores on this scale range from 0-20.
Timepoint [1] 302118 0
Week 12
Secondary outcome [1] 334849 0
Diagnosis of an anxiety disorder, as diagnosed by the Structured Clinical Interview for DSM-5.
Timepoint [1] 334849 0
Week 12
Secondary outcome [2] 334850 0
The Clinical Global Impression–Improvement (CGI-I) scale, which ranges from 1 to 7, with lower scores indicating more improvement, as compared with baseline. A score of 1 or 2 reflects a substantial, clinically meaningful improvement in anxiety severity.
Timepoint [2] 334850 0
Week 12
Secondary outcome [3] 334851 0
The Hamilton Anxiety Rating (HAM-A) is is one of the most used composite rating scales to measure anxiety in both clinical and research settings. It is clinician-rated and consists of 14 items, each defined by a series of symptoms, and measures both psychic anxiety (mental agitation and psychological distress) and somatic anxiety (physical complaints related to anxiety).
Timepoint [3] 334851 0
Week 12
Secondary outcome [4] 334852 0
The Quick Inventory Depression Symptomatology (QIDS) assesses the criterion symptom domains for DSM-5 major depressive disorder. The scale has been shown to be a reliable tool for assessing adolescent depression, making it one of the few depression scales that has been validated across adolescent and adult populations.
Timepoint [4] 334852 0
Week 12
Secondary outcome [5] 334853 0
The Social and Occupational Functional Assessment Scale (SOFAS) is a widely-used global rating of current functioning, ranging from 0 to 100, with lower scores representing lower functioning.
Timepoint [5] 334853 0
Week 12
Secondary outcome [6] 334854 0
The Cannabis Withdrawal Scale (CWS) assess any symptoms of withdrawal as the study medication is ceased.
Timepoint [6] 334854 0
Weeks 13
Secondary outcome [7] 334911 0
Adverse events (AEs), assessed with non-leading questions. Known AEs of CBD include sleepiness/mild sedation, decreased or increased appetite, diarrhea and fatigue.
Timepoint [7] 334911 0
Week 12
Secondary outcome [8] 335553 0
Serious AEs (SAEs), assessed with non-leading questions. Known SAEs include convulsion.
Timepoint [8] 335553 0
Week 12

Eligibility
Key inclusion criteria
(1) age 12-25 inclusive;
(2) ability to give informed consent and adhere to study procedures
(parental or guardian consent will be obtained for those under the age of 18);
(3) sufficient fluency in English;
(4) diagnosis of a DSM-5 anxiety disorder (i.e., social anxiety
disorder, panic disorder, separation anxiety disorder, specific
phobia, agoraphobia, generalized anxiety disorder);
(5) failure to show substantial, clinically meaningful improvement in anxiety severity during the last 8 to 16 weeks of CBT (minimum of 5 sessions), indicated by a score of 3 or higher on the Clinical Global Impression–Improvement scale (the CGI rating
will be provided by the CBT therapist)
Minimum age
12 Years
Maximum age
25 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
(1) DSM-5 schizophrenia spectrum disorder, delusional disorder, bipolar I disorder, substance/medication induced psychotic disorder;
(2) prior sensitivity or allergy to CBD or any cannabis-derived product;
(3) current treatment with antipsychotic medication, anxiolytic medication or mood stabiliser; or any medication that either interacts with the metabolism of CBD or is affected by CBD and in the view of the study doctor cannot be co-administered safely
(4) if prescribed antidepressive medication, the individual must have been on a stable and sufficient dose for a minimum of 6 weeks;
(5) pregnancy, lactation, or if sexually active, no effective contraception;
(6) haematological findings that result in medically significant liver, thyroid or other conditions
(7) acute or unstable systemic medical disorder;
(8) psychiatric condition due to a medical condition;
(9) acute suicidality
(10) previous or current severe drug or severe alcohol dependence;
(11) severe disturbance, such that the person is unable to comply
with either the requirements of informed consent or the treatment protocol





(6) haematological findings that result in medically significant liver, thyroid or other conditions

(9) acute suicidality

(10) previous or current severe drug or severe alcohol dependence;

Study design
Purpose of the study
Treatment
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
N/A
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
N/A
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Open-label study.
Phase
Phase 2
Type of endpoint/s
Safety/efficacy
Statistical methods / analysis
The main analysis will be based on all enrolled participants with at least one post-baseline observation (intention-to-treat population). The primary efficacy analysis will assess average differences for the primary outcome measure (OASIS total score) over the entire study period and will use a likelihood based mixed-effects model, repeated measures approach (MMRM).

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
16/05/2018
Actual
25/05/2018
Date of last participant enrolment
Anticipated
Actual
28/06/2019
Date of last data collection
Anticipated
31/12/2019
Actual
24/09/2019
Sample size
Target
30
Accrual to date
Final
31
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 8034 0
Headspace Glenroy - Glenroy
Recruitment postcode(s) [1] 16005 0
3046 - Glenroy

Funding & Sponsors
Funding source category [1] 296435 0
Charities/Societies/Foundations
Name [1] 296435 0
The Lambert Initiative for Cannabinoid Therapeutics
Country [1] 296435 0
Australia
Funding source category [2] 296461 0
Other
Name [2] 296461 0
Orygen, The National Centre for Excellence in Youth Mental Health
Country [2] 296461 0
Australia
Primary sponsor type
Other
Name
Orygen, The National Centre for Excellence in Youth Mental Health
Address
35 Poplar Road
Parkville, VIC 3052
Country
Australia
Secondary sponsor category [1] 295417 0
None
Name [1] 295417 0
Address [1] 295417 0
Country [1] 295417 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 297668 0
Bellberry Ltd.
Ethics committee address [1] 297668 0
Ethics committee country [1] 297668 0
Australia
Date submitted for ethics approval [1] 297668 0
12/05/2017
Approval date [1] 297668 0
05/09/2017
Ethics approval number [1] 297668 0
2017-02-107

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 74754 0
Prof G. Paul Amminger
Address 74754 0
Orygen, 35 Poplar Road, Parkville, VIC 3052
Country 74754 0
Australia
Phone 74754 0
+61 0399669100
Fax 74754 0
Email 74754 0
[email protected]
Contact person for public queries
Name 74755 0
Paul Amminger
Address 74755 0
Orygen, 35 Poplar Road, Parkville, VIC 3052
Country 74755 0
Australia
Phone 74755 0
+61 0399669100
Fax 74755 0
Email 74755 0
[email protected]
Contact person for scientific queries
Name 74756 0
G. Paul Amminger
Address 74756 0
Orygen, 35 Poplar Road, Parkville, VIC 3052
Country 74756 0
Australia
Phone 74756 0
+61 0399669100
Fax 74756 0
Email 74756 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
What data in particular will be shared?
All data, anonymised.
When will data be available (start and end dates)?
Data are available immediately for an indefinite time.
Available to whom?
Data will potentially be available to researchers from not-for profit organisations, commercial organisations or other based in any location. All data requests will be considered by the data custodian and the primary sponsor on a case-by-case basis. Requests must include a methodologically sound proposal. Specific conditions of use may apply and will be specified in a data sharing agreement (or similar) that the requester must agree to before access is granted. For further information, see Orygen data management policy.
Available for what types of analyses?
To any type of analyses. Assessed on a case-by-case basis
How or where can data be obtained?
Access can be requested via the Health Data Australia catalogue (https://researchdata.edu.au/health). Search for the ANZTRN number in the catalogue to find datasets associated with this trial.


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
SourceTitleYear of PublicationDOI
EmbaseCannabidiol for Treatment-Resistant Anxiety Disorders in Young People: An Open-Label Trial.2022https://dx.doi.org/10.4088/JCP.21m14130
N.B. These documents automatically identified may not have been verified by the study sponsor.