search
Back to results

Non-Inferiority RCT Comparing Online and On-Site CBT in MDDi

Primary Purpose

Major Depressive Disorder

Status
Not yet recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Standard psychiatry and cognitive behavioral online intervention
Standard psychiatry and cognitive behavioural in-person intervention
Sponsored by
York University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Major Depressive Disorder focused on measuring internet-based intervention, major depressive disorder, health coaching

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Beck Depression Inventory-II of at least mild severity (BDI-II score ≥ 14) with no upper severity limit;
  • Psychiatrist diagnosis of Major Depression Disorder;
  • MINI International Neuropsychiatric Interview-confirmed diagnosis of Major Depression Disorder;
  • fluent in English.

Exclusion Criteria:

  • individuals currently receiving weekly structured psychotherapy;
  • individuals who meet DSM-V criteria for severe alcohol/substance use disorder (in the past 3 months), borderline personality disorder, schizophrenia or any other primary psychotic disorder, bipolar disorder or obsessive-compulsive disorder;
  • individuals who manifest clinically significant suicidal ideation defined as imminent intent or attempted suicide (in the past 6 months);
  • individuals who are judged to have treatment resistant depression (TRD), as defined by failure in at least two trials of antidepressant medications and/or a course of psychotherapy during the current depressive episode

Sites / Locations

  • York University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Standard psychiatry and cognitive behavioural online intervention

Standard psychiatry and cognitive behavioural in-person intervention

Arm Description

The online group CBT-M program combines software-based workbooks with phone-based Navigator-Coaching that coordinates software interactions (e.g., secure text messaging, Fitbit tracked walking, food monitoring via photography). Navigation coaching is supplied by students who were pursuing graduate degrees (MSc, MA, PhD) in kinesiology and health science, education, and psychology.

The on-site, usual-care CBT group follows the structure of the Mind Over Mood workbook in reviewing CBT concepts and procedures. A series of work sheets assist participants in differentiating moods, and in differentiating moods from thoughts and situational influences, leading to modifications of thinking, behaviour, emotion and mood. Group leaders are standard leaders in the CAMH group-CBT program who have Masters-level degrees in psychology, social work and occupational therapists.

Outcomes

Primary Outcome Measures

Change in Beck Depression Inventory - 2 (0 to 63 - higher score indicates worse outcome)
Frequently used and validated self report measure

Secondary Outcome Measures

Change in Beck Anxiety Inventory (0 to 63 - higher score indicates worse outcome)
Frequently used and validated self report measure
Change in Quick Inventory of Depressive Symptoms (0 to 48 - higher score indicates worse outcome)
Frequently used and validated self report measure
Change in Hamilton Depression Rating Scale - 24-item version (0 to 72) Hamilton Depression Rating Scale - 24 item (0 - 96 - higher score indicates worse outcome)
Frequently used and validated interview-based evaluation instrument
Change in 5-Facet Mindfulness Questionnaire - 39-item version (39 to 195 - higher score indicates better outcome) Five-Facet Mindfulness Questionnaire
Frequently used and validated self report measure
Change in Brief Pain Inventory - 11 item (0 - 176 - high score indicates worse outcome)
Frequently used and validated self report measure
Change in EQ-5D Quality of Life Instrument - 5 items - 0 - 25 - high score - worse outcome)
Frequently used and validated self report measure

Full Information

First Posted
March 21, 2021
Last Updated
March 30, 2021
Sponsor
York University
search

1. Study Identification

Unique Protocol Identification Number
NCT04825535
Brief Title
Non-Inferiority RCT Comparing Online and On-Site CBT in MDDi
Official Title
A Non-Inferiority Randomized Controlled Trial Comparing Online and On-Site Cognitive Behaviour Therapy in Major Depressive Disorder
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Not yet recruiting
Study Start Date
April 2021 (Anticipated)
Primary Completion Date
April 2025 (Anticipated)
Study Completion Date
April 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
York University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
In recent years, Cognitive Behavioral Therapy has been integrated with mindfulness meditation (CBT-M) following evidence for increased efficacy when modalities are combined. We will assess whether online group CBT-M plus standard psychiatric care is non-inferior in efficacy and more cost-effective than office-based, on-site group CBT-M (plus standard psychiatric care) per outcomes at post-intervention and at 6-month follow up in adults with major depressive disorder (MDD). This non-inferiority randomized controlled trial will employ both assessor-blinded and self-report outcome measures and will include a full economic evaluation.
Detailed Description
Depression is a commonly diagnosed mental health disorder that represents the most prevalent cause of disability worldwide. Cognitive Behavioural Therapy (CBT) is the best-evidenced treatment for depression, but despite demonstrated efficacy, many individuals cannot access adequate psychotherapeutic treatment due to the limitations of face-to-face delivery. In recent years, CBT has been integrated with mindfulness meditation (CBT-M) following strong evidence for increased efficacy when the two modalities are combined. Previous RCTs have demonstrated that online CBT-M is effective in depressive symptom reduction, but direct comparisons to in-office CBT delivery assessing cost and treatment outcomes are required to facilitate innovation and clinical policy change. Objectives: To assess whether online group CBT-M plus standard psychiatric care is non-inferior in efficacy and more cost-effective than office-based, on-site group CBT-M (plus standard psychiatric care) per outcomes at post-intervention and at 6-month follow up in adults diagnosed with major depressive disorder (MDD). The study will assess whether digitally recorded adherence data (i.e. online workbooks completed, Fitbit tracked step count, online text-messages exchanged, phone sessions completed) predict outcome benefits in the online-group participants as measured by changes in depressive symptoms. Methods: This single-centre, 2-arm non-inferiority randomized controlled trial will employ both assessor-blinded and self-report outcome measures and will include a full economic evaluation. The research site is the Centre for Addiction and Mental Health (CAMH), a large research-based psychiatry institution located in Toronto, Canada. Participants will be identified from wait-lists for CAMH services and through contacts with other Toronto outpatient clinics. Interventions: All participants will receive standard psychiatric care (1 pharmacotherapy focused visit/month with a psychiatrist of 15-30 minute duration). Experimental participants additionally receive online CBT-M while control participants receive standard care in-office group CBT-M. The online group CBT-M program (in collaboration with NexJ Health, Inc.) combines exposure to smartphone and computer accessed workbooks with phone-based mental health counselling (16 hours in 16 weeks) that coordinates with ongoing software interactions (e.g. secure text messaging, Fitbit tracked walking). Each participant is loaned a Fitbit-HR Charge 3 to assess physical activity as measured by daily step count.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Depressive Disorder
Keywords
internet-based intervention, major depressive disorder, health coaching

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Online CBT intervention
Masking
Outcomes Assessor
Masking Description
One assessor will be blinded to the (2) comparison groups of all participants.
Allocation
Randomized
Enrollment
156 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Standard psychiatry and cognitive behavioural online intervention
Arm Type
Experimental
Arm Description
The online group CBT-M program combines software-based workbooks with phone-based Navigator-Coaching that coordinates software interactions (e.g., secure text messaging, Fitbit tracked walking, food monitoring via photography). Navigation coaching is supplied by students who were pursuing graduate degrees (MSc, MA, PhD) in kinesiology and health science, education, and psychology.
Arm Title
Standard psychiatry and cognitive behavioural in-person intervention
Arm Type
Active Comparator
Arm Description
The on-site, usual-care CBT group follows the structure of the Mind Over Mood workbook in reviewing CBT concepts and procedures. A series of work sheets assist participants in differentiating moods, and in differentiating moods from thoughts and situational influences, leading to modifications of thinking, behaviour, emotion and mood. Group leaders are standard leaders in the CAMH group-CBT program who have Masters-level degrees in psychology, social work and occupational therapists.
Intervention Type
Behavioral
Intervention Name(s)
Standard psychiatry and cognitive behavioral online intervention
Intervention Description
The cognitive behavioral online intervention has been assessed in a prior trial. Ritvo, P, Knyahnytska, Y, Pirboglou, M, Wang, W, Tomlinson, G, Zhao, H, Linklater, R, Kirk, M., Katz, J., Harber, L., Daskalakis, ZJ An online mindfulness-based cognitive behavioural therapy intervention for youth diagnosed with major depressive disorders: J Med Internet Res 2021, Mar 17; 23 (3), e24380
Intervention Type
Behavioral
Intervention Name(s)
Standard psychiatry and cognitive behavioural in-person intervention
Intervention Description
The effectiveness of standard care office-based group CBT-MM at CAMH is indicated in a past study (n = 119) where depression symptoms reduced (after 16 weeks treatment) by 27% [3,18 ]. The office-based groups follow a carefully conceived structure that centers on the workbook Mind Over Mood (MOM) (Guilford Press) [41]. Key CBT concepts and procedures are conveyed via work sheets that structure personal and group exploration.
Primary Outcome Measure Information:
Title
Change in Beck Depression Inventory - 2 (0 to 63 - higher score indicates worse outcome)
Description
Frequently used and validated self report measure
Time Frame
Baseline and 4 months
Secondary Outcome Measure Information:
Title
Change in Beck Anxiety Inventory (0 to 63 - higher score indicates worse outcome)
Description
Frequently used and validated self report measure
Time Frame
Baseline and 4 months
Title
Change in Quick Inventory of Depressive Symptoms (0 to 48 - higher score indicates worse outcome)
Description
Frequently used and validated self report measure
Time Frame
Baseline and 4 months
Title
Change in Hamilton Depression Rating Scale - 24-item version (0 to 72) Hamilton Depression Rating Scale - 24 item (0 - 96 - higher score indicates worse outcome)
Description
Frequently used and validated interview-based evaluation instrument
Time Frame
Baseline and 4 months
Title
Change in 5-Facet Mindfulness Questionnaire - 39-item version (39 to 195 - higher score indicates better outcome) Five-Facet Mindfulness Questionnaire
Description
Frequently used and validated self report measure
Time Frame
Baseline and 4 months
Title
Change in Brief Pain Inventory - 11 item (0 - 176 - high score indicates worse outcome)
Description
Frequently used and validated self report measure
Time Frame
Baseline and 4 months
Title
Change in EQ-5D Quality of Life Instrument - 5 items - 0 - 25 - high score - worse outcome)
Description
Frequently used and validated self report measure
Time Frame
Baseline and 4 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Beck Depression Inventory-II of at least mild severity (BDI-II score ≥ 14) with no upper severity limit; Psychiatrist diagnosis of Major Depression Disorder; MINI International Neuropsychiatric Interview-confirmed diagnosis of Major Depression Disorder; fluent in English. Exclusion Criteria: individuals currently receiving weekly structured psychotherapy; individuals who meet DSM-V criteria for severe alcohol/substance use disorder (in the past 3 months), borderline personality disorder, schizophrenia or any other primary psychotic disorder, bipolar disorder or obsessive-compulsive disorder; individuals who manifest clinically significant suicidal ideation defined as imminent intent or attempted suicide (in the past 6 months); individuals who are judged to have treatment resistant depression (TRD), as defined by failure in at least two trials of antidepressant medications and/or a course of psychotherapy during the current depressive episode
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Paul Ritvo, PhD
Phone
4167362100
Ext
22396
Email
pritvo@yorku.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Clarice Walters, BSc
Phone
4167682002
Email
clarice.walters@camh.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paul Ritvo
Organizational Affiliation
York University
Official's Role
Principal Investigator
Facility Information:
Facility Name
York University
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M3J 1P3
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
No. We may consider investigators who wish to use data in further analyses but we cannot guarantee access.
Citations:
PubMed Identifier
35393942
Citation
Ritvo P, Gratzer D, Knyahnytska Y, Ortiz A, Walters C, Katz J, Laposa J, Baldissera C, Wayne N, Pfefer-Litman D, Tomlinson G, Daskalakis Z. Comparing Online and On-Site Cognitive Behavior Therapy in Major Depressive Disorder: Protocol for a Noninferiority Randomized Controlled Trial. JMIR Res Protoc. 2022 Apr 8;11(4):e29726. doi: 10.2196/29726. Erratum In: JMIR Res Protoc. 2022 Apr 21;11(4):e38720.
Results Reference
derived

Learn more about this trial

Non-Inferiority RCT Comparing Online and On-Site CBT in MDDi

We'll reach out to this number within 24 hrs