Study Stopped
Sponsor pulled out of study
Mindbeacon Therapist Assisted Internet Delivered CBT for Depression
A 12-week Randomized Waitlist-Controlled Trial of Mindbeacon Therapist Assisted Internet Delivered CBT for Depression
1 other identifier
interventional
N/A
0 countries
N/A
Brief Summary
Utilization of therapist Assisted internet-delivered cognitive behavioural therapy (TAiCBT) for treating depression and anxiety disorders in stepped-care models, such as the UK's Improving Access to Psychological Therapies (IAPT) and the Ontario Structured Psychotherapy Program (SPP), is a potential solution for addressing the treatment gap in mental health. Investigators propose to investigate the effectiveness of Beacon TAiCBT for Depression to demonstrate the potential value of TAiCBT in a stepped care model. Investigators propose to conduct a 12-week pragmatic randomized controlled trial with a 1:1 (iCBT intervention: waiting-list) allocation, for participants referred to the Anxiety and Mood, Prompt Anxiety and Mood, and Trauma Programs at Ontario Shores Centre for Mental Health Sciences and on a waiting-list to receive clinical service. The primary outcome measures will be the Improving Access to Psychological Therapies (IAPT) definitions of Recovery, Reliable Improvement, and Reliable Recovery which are derived using the PHQ-9 and GAD-7 . The PHQ-9 (Depression), GAD-7 (anxiety) and WSAS (functional impairment) will be used as secondary outcome measures for all participants. Over the course of the study, 200 participants will be randomized (iCBT, 100; waiting-list, 100). Statistical analyses will include intention-to-treat analyses to test the interaction effects for the primary outcome measures at discharge/12-weeks and 3, and 12 months post-treatment. It is predicted that participants in the treatment condition will show significantly reduced symptoms of depression related to the waitlist control. It is predicted that this will be maintained through follow up.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started Nov 2021
Shorter than P25 for not_applicable major-depressive-disorder
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 5, 2021
CompletedStudy Start
First participant enrolled
November 1, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 18, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
November 18, 2021
CompletedFirst Posted
Study publicly available on registry
November 24, 2021
CompletedApril 18, 2023
April 1, 2023
17 days
October 5, 2021
April 14, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (9)
IAPT Definition of "Recovery" (Change between Baseline and Post-treatment)
The IAPT criteria for 'Recovery' are met when patients move from 'caseness' at the beginning of the intervention (e.g., scoring \>9 on the PHQ-9 or \>7 on the GAD-7) to 'non-caseness' at the end of treatment (thus scoring below the cut-off)
GAD-7 and PHQ-9 which are used to compute this outcome measure are administered at baseline (initial screening) and "post-treatment" which is week 12 of treatment)
IAPT Definition of "Recovery" (Change between baseline and 3 month follow-up)
The IAPT criteria for 'Recovery' are met when patients move from 'caseness' at the beginning of the intervention (e.g., scoring \>9 on the PHQ-9 or \>7 on the GAD-7) to 'non-caseness' at the end of treatment (thus scoring below the cut-off)
GAD-7 and PHQ-9 which are used to compute this outcome measure are administered at baseline (initial screening) and 3 month follow-up (3 months after "post-treatment" which is week 12 of treatment)
IAPT Definition of "Recovery" (Change between baseline and 12 month follow-up)
The IAPT criteria for 'Recovery' are met when patients move from 'caseness' at the beginning of the intervention (e.g., scoring \>9 on the PHQ-9 or \>7 on the GAD-7) to 'non-caseness' at the end of treatment (thus scoring below the cut-off)
GAD-7 and PHQ-9 which are used to compute this outcome measure are administered at baseline (initial screening) and 12 month follow-up (12 months after "post-treatment" which is week 12 of treatment)
IAPT Definition of "Reliable improvement" (Change between Baseline and Post-treatment)
Reliable improvement is defined as when the patient has a 'reliable' decrease in their PHQ-9 / GAD-7 (reduction in PHQ-9 score of 6 or more, and reduction in GAD-7 score of 4 or more) score upon completion of their course of treatment
GAD-7 and PHQ-9 which are used to compute this outcome measure are administered at baseline (initial screening) and "post-treatment" which is week 12 of treatment)
IAPT Definition of "Reliable improvement" (Change between baseline, and 3 month follow-up)
Reliable improvement is defined as when the patient has a 'reliable' decrease in their PHQ-9 / GAD-7 (reduction in PHQ-9 score of 6 or more, and reduction in GAD-7 score of 4 or more) score upon completion of their course of treatment
GAD-7 and PHQ-9 which are used to compute this outcome measure are administered at baseline (initial screening) and 3 month follow-up (3 months after "post-treatment" which is week 12 of treatment)
IAPT Definition of "Reliable improvement" (Change between baseline and 12 month follow-up)
Reliable improvement is defined as when the patient has a 'reliable' decrease in their PHQ-9 / GAD-7 (reduction in PHQ-9 score of 6 or more, and reduction in GAD-7 score of 4 or more) score upon completion of their course of treatment
GAD-7 and PHQ-9 which are used to compute this outcome measure are administered at baseline (initial screening) and 12 month follow-up (12 months after "post-treatment" which is week 12 of treatment)
IAPT definition of "Reliable recovery" (Change between Baseline and Post-treatment)
Reliable recovery is defined as when the patient meets the criteria for both recovery and reliable improvement as defined above. Thus, a patient who moves from caseness to non-caseness, and also shows a 'reliable' (reduction in PHQ-9 score of 6 or more, and reduction in GAD-7 score of 4 or more) decrease in their symptom scores, is said to have a reliable recovery
GAD-7 and PHQ-9 which are used to compute this outcome measure are administered at baseline (initial screening) and post-treatment (week 12 of treatment)
IAPT definition of "Reliable recovery" (Change between baseline and 3 month follow-up)
Reliable recovery is defined as when the patient meets the criteria for both recovery and reliable improvement as defined above. Thus, a patient who moves from caseness to non-caseness, and also shows a 'reliable' (reduction in PHQ-9 score of 6 or more, and reduction in GAD-7 score of 4 or more) decrease in their symptom scores, is said to have a reliable recovery
GAD-7 and PHQ-9 which are used to compute this outcome measure are administered at baseline (initial screening) and 3 month follow-up (3 months after "post-treatment" which is week 12 of treatment)
IAPT definition of "Reliable recovery" (Change between baseline and 12 month follow-up)
Reliable recovery is defined as when the patient meets the criteria for both recovery and reliable improvement as defined above. Thus, a patient who moves from caseness to non-caseness, and also shows a 'reliable' (reduction in PHQ-9 score of 6 or more, and reduction in GAD-7 score of 4 or more) decrease in their symptom scores, is said to have a reliable recovery
GAD-7 and PHQ-9 which are used to compute this outcome measure are administered at baseline (initial screening) and 12 month follow-up (12 months after "post-treatment" which is week 12 of treatment)
Secondary Outcomes (9)
Work and Social Adjustment Scale (WSAS) - (Change between Baseline and Post-treatment)
Administered at baseline (initial screening) and post-treatment (week 12 of treatment)
Work and Social Adjustment Scale (WSAS) - (Change between baseline and 3 month follow-up)
Administered at baseline (initial screening) and 3 month follow-up (3 months after "post-treatment" which is week 12 of treatment)
Work and Social Adjustment Scale (WSAS) - (Change between baseline and 12 month follow-up)
Administered at baseline (initial screening) and 12 month follow-up (12 months after "post-treatment" which is week 12 of treatment)
Patient Health Questionnaire 9 (PHQ-9) - (Change between baseline and post-treatment)
Administered at baseline (initial screening) and post-treatment (week 12 of treatment)
Patient Health Questionnaire 9 (PHQ-9) - (Change between baseline and 3 month follow-up)
Administered at baseline (initial screening) and 3 month follow-up (3 months after "post-treatment" which is week 12 of treatment)
- +4 more secondary outcomes
Study Arms (2)
Mindbeacon TAI-CBT for Depression group
EXPERIMENTALParticipants randomized to this condition will receive immediate Therapist-Guided Internet-CBT for Depression for 12 weeks.
Waitlist Control Group
OTHERParticipants randomized to this condition will remain on the waitlist for 12 weeks before crossing over and receiving Therapist-Guided Internet-CBT for Depression for 12 weeks.
Interventions
The treatment consists of 11 depression modules delivered approximately once per week (at therapists' discretion) over a period of 12 weeks. Additionally, the therapist typically tailors treatment to client's individual needs by including supplementary modules for a variety of issues such as generalized anxiety, panic, social anxiety, post-traumatic stress, insomnia, pain, and relationships etc. Clients can complete the readings, exercises, and worksheets at any convenient time, using their web-enabled smartphone, tablet, or computer. Access to the modules and all messaging is provided through the secure platform. Messaging is "asynchronous" meaning participants can message their therapist as often as they choose and expect a response within 1-2 business days. After 12 weeks of active treatment, they will have unguided access (without therapist support) to the treatment materials that were covered for an additional 40 weeks.
Participants assigned to this arm will wait for 12 weeks before receiving active treatment condition
Eligibility Criteria
You may qualify if:
- Minimum age of 18 years
- Meets Diagnostic Assessment Research Tool (DART) screening criteria for a primary diagnosis of depression and reports being at least moderately depressed according to the PHQ-9
- Sufficient language proficiency to understand the treatment materials written at grade 10 reading level
- Understands what TAiCBT and is open and interested to participating in a study using this treatment modality
- Is able to reliably access the internet, and has basic computer skills to navigate the internet using a web browser
- Willing to participate in a waitlist-control study and be followed for 12 months
You may not qualify if:
- Suicidal intent or clinically significant suicidal ideation
- Clinically significant self-harm
- Active psychotic illness
- Currently participating in psychological treatment for depression and/or receiving evidence-based treatment (other than medication) for depression
- Clinically significant alcohol and/or other substance use including prescription and over the counter medication that would likely interfere with treatment
- Current or previous diagnosis of Borderline Personality Disorder
- Does not meet DART criteria for a primary diagnosis of depression
- Change in psychotropic medication within 3 weeks of treatment baseline
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Ontario Shores Centre for Mental Health Scienceslead
- Mindbeaconcollaborator
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Phil Klassen, MD
Ontario Shores Hospital
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 5, 2021
First Posted
November 24, 2021
Study Start
November 1, 2021
Primary Completion
November 18, 2021
Study Completion
November 18, 2021
Last Updated
April 18, 2023
Record last verified: 2023-04
Data Sharing
- IPD Sharing
- Will not share
Individual Participant Data will not be shared with other researchers. Anonymized/deidentified aggregate data for the study may be shared.