NCT05134103

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

15
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Timeline
Completed

Started Nov 2021

Shorter than P25 for not_applicable major-depressive-disorder

Status
withdrawn

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

Completed
27 days until next milestone

Study Start

First participant enrolled

November 1, 2021

Completed
17 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 18, 2021

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 18, 2021

Completed
6 days until next milestone

First Posted

Study publicly available on registry

November 24, 2021

Completed
Last Updated

April 18, 2023

Status Verified

April 1, 2023

Enrollment Period

17 days

First QC Date

October 5, 2021

Last Update Submit

April 14, 2023

Conditions

Keywords

Depression

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

EXPERIMENTAL

Participants randomized to this condition will receive immediate Therapist-Guided Internet-CBT for Depression for 12 weeks.

Behavioral: Mindbeacon Therapist Guided, Internet Cognitive Behavioral Therapy for Depression

Waitlist Control Group

OTHER

Participants 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.

Other: Waitlist Control Group

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.

Also known as: Internet-CBT
Mindbeacon TAI-CBT for Depression group

Participants assigned to this arm will wait for 12 weeks before receiving active treatment condition

Waitlist Control Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

MeSH Terms

Conditions

Depressive Disorder, MajorDepression

Condition Hierarchy (Ancestors)

Depressive DisorderMood DisordersMental DisordersBehavioral SymptomsBehavior

Study Officials

  • Phil Klassen, MD

    Ontario Shores Hospital

    PRINCIPAL INVESTIGATOR
0

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
CROSSOVER
Model Details: This is a waitlist-controlled, randomized controlled trial.
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.