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Outcomes From Remediation and Behavioural Intervention Techniques (ORBIT)

Primary Purpose

Schizophrenia, Psychosis, Psychotic Disorders

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Cognitive Behavioural Therapy for Psychosis (CBTp)
Cognitive Remediation Therapy (CR)
Befriending
Sham Cognitive Remediation
Sponsored by
University of Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Aged 18-65 years Diagnosed with schizophrenia-spectrum disorders Can read, write, and speak English Exclusion Criteria: Primary substance use disorder Neurodevelopmental disability or neurocognitive disorder Neurostimulation in the past 30 days CBT or CR in the past 6 months

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Experimental

    Experimental

    Experimental

    Arm Label

    Individual CBTp + Group Sham CR

    Group CR + Individual Befriending (Sham CBTp)

    Individual CBTp + Group CR

    Arm Description

    Individual formulation-based CBT will be delivered for one hour per week using a manual that has been validated in over 1000 individuals with schizophrenia-spectrum disorders across all stages of illness. Sham CR was developed by Dr. Best and Dr. Bowie (CI) to control for the non-specific effects of CR such as computer practice and group discussion.

    Action-based cognitive remediation (ABCR) will be delivered in group sessions one hour per week. ABCR was developed by Dr. Bowie (CI) and Dr. Best (PI) and has been found efficacious for schizophrenia-spectrum disorders in three clinical trials. Befriending will be delivered according to a manual validated to control for the non-specific effects of CBT, such as duration of therapeutic contact, client expectancy effects, therapeutic alliance, and therapist warmth.

    Individual formulation-based CBT will be delivered for one hour per week using a manual that has been validated in over 1000 individuals with schizophrenia-spectrum disorders across all stages of illness. Action-based cognitive remediation (ABCR) will be delivered in group sessions one hour per week. ABCR was developed by Dr. Bowie (CI) and Dr. Best (PI) and has been found efficacious for schizophrenia-spectrum disorders in three clinical trials.

    Outcomes

    Primary Outcome Measures

    Social Functioning Scale
    The Social Functioning Scale (SFS) is an interview-based measure administered to an informant and assesses domains of social engagement, interpersonal communication, independence, recreation, prosocial behavior, and vocational activities. Items have various scales and ways to interpret them since this is a longer, interview-based measure.

    Secondary Outcome Measures

    World Health Organization Quality of Life Scale Brief Version (WHOQOL-BREF)
    Quality of Life will be assessed using the World Health Organization Quality of Life Scale Brief Version (WHOQOL-BREF), which contains 26 items assessing 4 domains: physical health, psychological, social relationships, and environment. The WHOQOL-BREF is reliable and valid in schizophrenia.
    Questionnaire About the Process of Recovery
    Personal Recovery will be assessed using the Questionnaire About the Process of Recovery, a 15-item self-report measure collaboratively developed with service-users experiencing psychosis.
    Positive and Negative Syndrome Scale (PANSS)
    Psychiatric Symptoms will be assessed with the Positive and Negative Syndrome Scale (PANSS), the gold standard symptom interview for schizophrenia. The PANSS assesses positive, negative, and general symptoms, and a 15-point change on the PANSS is associated with clinically meaningful change.
    Psychotic Symptom Rating Scale (PSYRATS)
    The Psychotic Symptom Rating Scale (PSYRATS) is an interview assessing dimensions of hallucination and delusion severity that members of our team validated.
    MATRICS Consensus Cognitive Battery (MCCB)
    Neurocognition will be assessed using the MATRICS Consensus Cognitive Battery (MCCB), the gold standard assessment of cognitive functions for schizophrenia. The MCCB assesses domains of processing speed, sustained attention, verbal learning, visual learning, working memory, and reasoning / problem solving. Extensive normative data will be used to generate a global neurocognitive composite score.
    Beliefs About Paranoia Scale (BAPS)
    Assesses cognitive content. Each item was scored on a 4-point scale to measure conviction (1 = not at all, 2 = somewhat, 3 = moderately so, 4 = very much).
    Interpretations of Voices Inventory (IVI)
    Assesses cognitive content.
    Brief Core Schema Scale (BCSS)
    Assesses cognitive content. Participants indicate whether they hold each of the beliefs using No or Yes, and if they do hold the belief, they indicate how strongly they hold it by circling the numbers 1 to 4 (believe it slightly, believe it moderately, believe it very much, believe it totally).
    Defeatist Beliefs Scale (from Dysfunctional Attitudes Scale, DAS)
    Assesses cognitive content. The rating format for the 80 Dysfunctional Attitudes Scale items is a 7-point Likert scale ranging from totally agree to totally disagree. Possible responses are scored from 1 to 7, with the direction depending on whether agreement or disagreement with a particular belief is judged to be a maladaptive response, and with higher scores indicating more distorted thinking.
    Questionnaire on Healthcare Consumption and Productivity Losses for Patients with a Psychiatric Disorder (TiC-P)
    The TiC-P is a self-report measure that has been validated against objective health data.

    Full Information

    First Posted
    January 19, 2023
    Last Updated
    February 7, 2023
    Sponsor
    University of Toronto
    Collaborators
    Ontario Shores Centre for Mental Health Sciences, Queen's University, Centre for Addiction and Mental Health, University of British Columbia
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05731414
    Brief Title
    Outcomes From Remediation and Behavioural Intervention Techniques
    Acronym
    ORBIT
    Official Title
    Cognitive Behavioural Therapy Compared to Cognitive Remediation for Schizophrenia-Spectrum Disorders
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    March 1, 2023 (Anticipated)
    Primary Completion Date
    January 31, 2027 (Anticipated)
    Study Completion Date
    January 31, 2027 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of Toronto
    Collaborators
    Ontario Shores Centre for Mental Health Sciences, Queen's University, Centre for Addiction and Mental Health, University of British Columbia

    4. Oversight

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

    5. Study Description

    Brief Summary
    It is currently unknown what factors predict response to Cognitive Behavioural Therapy for Psychosis (CBTp) or Cognitive Remediation Therapy (CR) among individuals with schizophrenia-spectrum disorders, thus the current trial will examine predictors of response to determine who requires the combined intervention and who might respond sufficiently to either monotherapy.
    Detailed Description
    Dominant treatment approaches for schizophrenia-spectrum disorders improve psychiatric symptoms but do little to improve community functioning, leading to persistent disability and substantial economic burden. The proposed trial aims to examine the efficacy of a multi-mechanism approach to combining CBT and CR with the goal of predicting treatment response to either monotherapy or combination therapy. To date, there have been no randomized controlled trials examining the combination of CBT and CR. Given the differential mechanisms of CBT and CR, the combined multi-mechanism approach is expected to more effectively improve functional recovery than either monotherapy. Additionally, it is currently unknown what factors predict response to CBT or CR, thus the current trial will examine predictors of response to determine who requires the combined intervention and who might respond sufficiently to either monotherapy. The proposed trial will be one of the largest trials of psychosocial interventions for schizophrenia-spectrum disorders ever conducted and will simultaneously evaluate the combined intervention and moderators of differential treatment response. Narrower fields of inquiry examining mono-mechanism interventions have demonstrated little utility in improving functional recovery in schizophrenia, thus, the proposed approach represents a critical advancement by examining the utility of a multi-mechanism cognitive intervention and determining characteristics of those requiring this level of treatment. The goals of the current study are three-fold: Examine the efficacy of combining CBT and CR on the primary outcome of community functioning, and secondary outcomes of quality of life, personal recovery, psychiatric symptoms, and neurocognition compared to either intervention alone. Examine demographic, cognitive, and psychological factors that predict differential response to CBT, CR, or combined CBT and CR. Examine the specificity of cognitive content and cognitive functions as therapeutic mechanisms in CBT and CR respectively.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Schizophrenia, Psychosis, Psychotic Disorders, Schizophrenia; Psychosis

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Participants will be randomized to receive a) individual CBT + group sham CR, b) group CR + individual Befriending, or c) individual CBT + group CR. Block, cohort randomization will be coordinated by the trial manager at the central site (UTSC), with stratification by treatment site. Cohorts of 5 participants will be randomized to one of the 3 treatment conditions in randomized block sizes of 4, 8, or 12 using a pre-specified randomization list.
    Masking
    ParticipantInvestigatorOutcomes Assessor
    Masking Description
    This will be a double-blind (participant, assessor) trial. Participants will be informed that they will receive one individual session and one group session of treatment per week but will not be told which group they are assigned to. Participants will be instructed not to talk about their therapy to the assessor but if the assessor becomes aware of group allocation, then a new assessor will be assigned for all follow-up assessments. Due to the nature of the interventions, it is not possible for therapists to be blind to treatment condition, however, therapist fidelity to each intervention will be monitored through ratings on established fidelity measures. To protect against contamination separate therapists will deliver the active and control therapies. The Principal Investigator also remains blind to randomization, as the trial manager is the only one who has access to this.
    Allocation
    Randomized
    Enrollment
    360 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Individual CBTp + Group Sham CR
    Arm Type
    Experimental
    Arm Description
    Individual formulation-based CBT will be delivered for one hour per week using a manual that has been validated in over 1000 individuals with schizophrenia-spectrum disorders across all stages of illness. Sham CR was developed by Dr. Best and Dr. Bowie (CI) to control for the non-specific effects of CR such as computer practice and group discussion.
    Arm Title
    Group CR + Individual Befriending (Sham CBTp)
    Arm Type
    Experimental
    Arm Description
    Action-based cognitive remediation (ABCR) will be delivered in group sessions one hour per week. ABCR was developed by Dr. Bowie (CI) and Dr. Best (PI) and has been found efficacious for schizophrenia-spectrum disorders in three clinical trials. Befriending will be delivered according to a manual validated to control for the non-specific effects of CBT, such as duration of therapeutic contact, client expectancy effects, therapeutic alliance, and therapist warmth.
    Arm Title
    Individual CBTp + Group CR
    Arm Type
    Experimental
    Arm Description
    Individual formulation-based CBT will be delivered for one hour per week using a manual that has been validated in over 1000 individuals with schizophrenia-spectrum disorders across all stages of illness. Action-based cognitive remediation (ABCR) will be delivered in group sessions one hour per week. ABCR was developed by Dr. Bowie (CI) and Dr. Best (PI) and has been found efficacious for schizophrenia-spectrum disorders in three clinical trials.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Cognitive Behavioural Therapy for Psychosis (CBTp)
    Intervention Description
    Individual formulation-based CBT will be delivered for one hour per week using a manual that has been validated in over 1000 individuals with schizophrenia-spectrum disorders across all stages of illness. This approach has demonstrated moderate to large improvements on symptoms and small to moderate effects on functioning. The first four sessions are devoted to building therapeutic rapport and developing collaborative treatment goals. The following phase focuses on developing formulations of why difficulties persist and using cognitive and behavioural change strategies. A longitudinal formulation is then offered to better understand how their difficulties developed. The final 2-4 sessions focus on consolidating the learning that occurred during treatment so that participants can maintain their improvement. Therapy homework is collaboratively assigned at the end of sessions to promote new learning in between sessions.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Cognitive Remediation Therapy (CR)
    Intervention Description
    Action-based cognitive remediation (ABCR) will be delivered in group sessions one hour per week. ABCR was developed by Dr. Bowie (CI) and Dr. Best (PI) and has been found efficacious for schizophrenia-spectrum disorders in three clinical trials. ABCR involves practicing computerized training exercises with difficulty level dynamically titrated to improve neurocognitive abilities. Then participants engage in strategy discussions with other group members to develop new cognitive strategies. Finally, participants complete role-play simulations of real-world activities to practice their cognitive strategies in simulations of everyday life. ABCR is more effective for improving functioning than traditional approaches to CR. Homework consists of additional cognitive training and practicing cognitive strategies in everyday life.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Befriending
    Intervention Description
    Befriending will be delivered according to a manual validated to control for the non-specific effects of CBT, such as duration of therapeutic contact, client expectancy effects, therapeutic alliance, and therapist warmth. Befriending consists of 1-hour individual sessions once per week and involves a series of conversations similar to those one might have with a social acquaintance. These conversations involve discussion of neutral topics without problem-solving, coping strategies, or exploration of emotion. If emotional or mental health-related topics are brought up therapists redirect back to a neutral topic.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Sham Cognitive Remediation
    Intervention Description
    Sham CR was developed by Dr. Best and Dr. Bowie (CI) to control for the non-specific effects of CR such as computer practice and group discussion. Participants practice similar computerized exercises to ABCR, however, the exercises do not increase in difficulty. Participants then discuss enjoyment of the exercises but any discussion of cognitive strategies is redirected back to a neutral topic. We have previously found this condition to be an effective control for CR, with similar engagement to the active training group.
    Primary Outcome Measure Information:
    Title
    Social Functioning Scale
    Description
    The Social Functioning Scale (SFS) is an interview-based measure administered to an informant and assesses domains of social engagement, interpersonal communication, independence, recreation, prosocial behavior, and vocational activities. Items have various scales and ways to interpret them since this is a longer, interview-based measure.
    Time Frame
    Change between baseline assessment and 18-month assessment
    Secondary Outcome Measure Information:
    Title
    World Health Organization Quality of Life Scale Brief Version (WHOQOL-BREF)
    Description
    Quality of Life will be assessed using the World Health Organization Quality of Life Scale Brief Version (WHOQOL-BREF), which contains 26 items assessing 4 domains: physical health, psychological, social relationships, and environment. The WHOQOL-BREF is reliable and valid in schizophrenia.
    Time Frame
    Change between baseline assessment and 18-month assessment
    Title
    Questionnaire About the Process of Recovery
    Description
    Personal Recovery will be assessed using the Questionnaire About the Process of Recovery, a 15-item self-report measure collaboratively developed with service-users experiencing psychosis.
    Time Frame
    Change between baseline assessment and 18-month assessment
    Title
    Positive and Negative Syndrome Scale (PANSS)
    Description
    Psychiatric Symptoms will be assessed with the Positive and Negative Syndrome Scale (PANSS), the gold standard symptom interview for schizophrenia. The PANSS assesses positive, negative, and general symptoms, and a 15-point change on the PANSS is associated with clinically meaningful change.
    Time Frame
    Change between baseline assessment and 18-month assessment
    Title
    Psychotic Symptom Rating Scale (PSYRATS)
    Description
    The Psychotic Symptom Rating Scale (PSYRATS) is an interview assessing dimensions of hallucination and delusion severity that members of our team validated.
    Time Frame
    Change between baseline assessment and 18-month assessment
    Title
    MATRICS Consensus Cognitive Battery (MCCB)
    Description
    Neurocognition will be assessed using the MATRICS Consensus Cognitive Battery (MCCB), the gold standard assessment of cognitive functions for schizophrenia. The MCCB assesses domains of processing speed, sustained attention, verbal learning, visual learning, working memory, and reasoning / problem solving. Extensive normative data will be used to generate a global neurocognitive composite score.
    Time Frame
    Change between baseline assessment and 18-month assessment
    Title
    Beliefs About Paranoia Scale (BAPS)
    Description
    Assesses cognitive content. Each item was scored on a 4-point scale to measure conviction (1 = not at all, 2 = somewhat, 3 = moderately so, 4 = very much).
    Time Frame
    Change between baseline assessment and 18-month assessment
    Title
    Interpretations of Voices Inventory (IVI)
    Description
    Assesses cognitive content.
    Time Frame
    Change between baseline assessment and 18-month assessment
    Title
    Brief Core Schema Scale (BCSS)
    Description
    Assesses cognitive content. Participants indicate whether they hold each of the beliefs using No or Yes, and if they do hold the belief, they indicate how strongly they hold it by circling the numbers 1 to 4 (believe it slightly, believe it moderately, believe it very much, believe it totally).
    Time Frame
    Change between baseline assessment and 18-month assessment
    Title
    Defeatist Beliefs Scale (from Dysfunctional Attitudes Scale, DAS)
    Description
    Assesses cognitive content. The rating format for the 80 Dysfunctional Attitudes Scale items is a 7-point Likert scale ranging from totally agree to totally disagree. Possible responses are scored from 1 to 7, with the direction depending on whether agreement or disagreement with a particular belief is judged to be a maladaptive response, and with higher scores indicating more distorted thinking.
    Time Frame
    Change between baseline assessment and 18-month assessment
    Title
    Questionnaire on Healthcare Consumption and Productivity Losses for Patients with a Psychiatric Disorder (TiC-P)
    Description
    The TiC-P is a self-report measure that has been validated against objective health data.
    Time Frame
    Change between baseline assessment and 18-month assessment

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Aged 18-65 years Diagnosed with schizophrenia-spectrum disorders Can read, write, and speak English Exclusion Criteria: Primary substance use disorder Neurodevelopmental disability or neurocognitive disorder Neurostimulation in the past 30 days CBT or CR in the past 6 months
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Felicia Martins, HBSc
    Phone
    6476896098
    Ext
    100
    Email
    felicia.martins@mail.utoronto.ca
    First Name & Middle Initial & Last Name or Official Title & Degree
    Michael W Best, PhD, C.Psych
    Phone
    6476014551
    Email
    m.best@utoronto.ca
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Michael W Best, PhD, C.Psych
    Organizational Affiliation
    University of Toronto Scarborough
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Outcomes From Remediation and Behavioural Intervention Techniques

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