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Cognitive Behavioural Therapy- Social Functioning In Adolescence With Recent Onset Schizophrenia (Social)

Primary Purpose

Psychotic Disorders

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
CBT-SA
Standard Treatment
Sponsored by
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Psychotic Disorders

Eligibility Criteria

18 Years - 35 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. recent onset schizophrenia or related disorder (start antipsychotic medication <2 yr);
  2. Social withdrawal (> 3 moderate severity on the PANSS N4; Passive/apathic social withdrawal; range 0-7);
  3. Aged 18-35 years;
  4. Fluent in Dutch
  5. IQ>70;
  6. Able and willing to give informed consent

Exclusion Criteria:

  1. Younger than eighteen years of age;
  2. No mastery of the Dutch language;
  3. Negative symptoms as a consequence of positive symptoms (e.g. withdrawal due to paranoid delusions). Positive symptoms as such are not an exclusion criterion; only when they are considered to be the primary cause of the negative symptoms, in which case CBT focused on positive symptoms or another type of intervention for positive symptoms is called for.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    CBT-SA

    Standard Treatment

    Arm Description

    Group sessions for 4 weeks, two sessions per week, 60 minutes per session, two trainers (a CBT therapist and a CBT assistant); eight participants, and; Individual sessions (crystallizing learned skills, focus on individual needs) during 6-8 weeks, one session per week, 45 minutes per session

    Participants in both study conditions will receive ST. Participants are hospitalized or attending day-treatment at the Department of Early Psychosis, Amsterdam, the psychosis department of the ABC team, Utrecht, Parnassia Den Haag and collaborating (local community) mental health centers.

    Outcomes

    Primary Outcome Measures

    Level of social engagement
    Level of social engagement as measured by experiences sampling method
    Negative symptoms
    Negative symptoms as measured with PANSS
    Negative symptoms
    Negative symptoms as measured with BNSS

    Secondary Outcome Measures

    Quality of Life
    Assessed with the AQoL
    Global functioning
    Assessed with the GAF
    Productivity losses
    Effects on ability to perform paid and unpaid work
    Positive and General Symptomatology
    As assessed with the PANSS
    Depression
    Depression as assessed with the Calgary Depression Scale for Schizophrenia
    Inhibition/ Activation
    Behavioural Inhibition/ Behavioural Activation Scales (BISBAS)
    Need for care
    Camberwell Assessment of Need

    Full Information

    First Posted
    July 6, 2017
    Last Updated
    July 12, 2017
    Sponsor
    Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
    Collaborators
    Arkin, Vroege Psychose ABC - Utrecht, Centrum Eerste Psychose, Utrecht, Netherlands, GGZ inGeest
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03217955
    Brief Title
    Cognitive Behavioural Therapy- Social Functioning In Adolescence With Recent Onset Schizophrenia
    Acronym
    Social
    Official Title
    Cognitive Behavioural Therapy- Social Functioning In Adolescence With Recent Onset Schizophrenia
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2017
    Overall Recruitment Status
    Completed
    Study Start Date
    May 6, 2014 (Actual)
    Primary Completion Date
    March 1, 2017 (Actual)
    Study Completion Date
    March 1, 2017 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
    Collaborators
    Arkin, Vroege Psychose ABC - Utrecht, Centrum Eerste Psychose, Utrecht, Netherlands, GGZ inGeest

    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
    Rationale: There is growing consensus that targeting negative symptoms such as social withdrawal is essential to be able to preserve social participation, thereby reducing the high yearly costs of schizophrenia. Aaron T. Beck, founder of Cognitive Behavioural Therapy (CBT), and colleagues have developed and investigated a new CBT approach, in which they target inactivity in a chronic schizophrenia population with severe negative symptoms The therapy is based on accumulating evidence that dysfunctional beliefs in conjunction with neurocognitive impairments can impede social functioning. These results suggest that CBT can be highly successful in establishing clinically meaningful improvements. However, the therapy has not yet been investigated in a recent-onset population. Objective: To evaluate the applicability and (cost-) effectiveness of a shortened, partly group based, Cognitive Behavioural Therapy focussing on social activation (CBTsa) in patients with recent onset schizophrenia. Hypotheses: 1) the investigators hypothesized that CBT focused on social activation (CBTsa) in a recent-onset population will result in a substantial reduction in severity of negative symptoms, in particular social withdrawal. 2) The investigators expected that CBTsa would lead to an improvement in terms of Quality of Life and overall functioning. 3) The investigators expected this intervention to result in a reduction in need for care and QALY gain as a consequence of improvement in symptoms and social functioning. Study design: Single blind randomized controlled trial with 6 month-follow up. Study population: Patients between 18 and 35 years old with negative symptoms of at least moderate severity, and who have been recently (< 2yrs) diagnosed with schizophrenia. Intervention (if applicable): Individual and group-based CBT intervention targeting social withdrawal. Main study parameters/endpoints: Change in negative symptoms, Social functioning, and quality of life, Productivity losses.
    Detailed Description
    There is growing consensus that targeting negative symptoms such as social withdrawal is essential to be able to preserve social participation; thereby reducing the high yearly costs of schizophrenia. Aaron T. Beck, founder of Cognitive Behavioural Therapy (CBT), and colleagues have developed and investigated a new CBT approach, in which they target inactivity in a chronic schizophrenia population with severe negative symptoms; a subgroup that has always believed to be highly treatment resistant. The therapy is based on accumulating evidence that dysfunctional beliefs in conjunction with neurocognitive impairments can impede functioning. Its primary focus is to help patients overcome isolation and inactivity, thereby improve quality of life, rather than primarily focussing on the reduction of psychotic symptoms. Grant, Beck and colleagues found that patients treated with CBT not only showed more improvement in global functioning than patients in the Standard Treatment condition, they also showed a greater reduction in avolition/apathy and psychotic symptoms. These results suggest that CBT can be highly successful in establishing clinically meaningful improvements. Thus far, this intervention had only been investigated in patients with chronic schizophrenia although there is increasing evidence that social withdrawal is also prominent in the early phase of the illness. Moreover, there is growing consensus that early intervention is more effective in improving illness course than intervention at a later stage of the illness. In the present study the investigators aimed to examine whether a relatively short, partly group based CBT targeting negative symptoms in recent-onset schizophrenia patients results in reduced social withdrawal, need for care and improvement in quality of life and in overall functioning compared to treatment as usual. Primary Objective: The primary aim of this project was to examine a shortened (+/- 20 sessions) and partly group-based version of the new and promising CBT approach tested in a chronic population (from now: 'Cognitive Behavioural Therapy - Social Activation' (CBTsa)), for its applicability and effectiveness in a recent-onset population. The CBTsa has been adjusted to the specific needs of the young recent-onset cohort. Secondary Objective(s): A secondary aim was explore the cost-effectiveness of this new intervention (i.e. the balance between costs and health outcomes for CBTsa compared with treatment as usual(ST). Hypotheses: CBT focused on social activation (CBTsa) will result in a substantial reduction in severity of negative symptoms, and in particular social withdrawal The intervention will result in a reduction in need for care and QALY gain as a consequence of improvement in symptoms and social functioning. CBTsa will lead to an improvement in terms of Quality of Life and overall functioning and symptomatology. Study Design The present study entails a single-blind two-level RCT directed at patients with recent onset schizophrenia. Participants will be randomly assigned to intervention condition (Cognitive Behavioral Therapy- Social Activation (CBTsa) plus Standard Treatment (ST)), or to the control condition (ST alone). Patients will be stratified by sex, as females with recent onset schizophrenia have a better prognosis and may respond differentially to CBTsa. A baseline test battery will be employed to examine causes of social withdrawal and interaction with treatment outcome. Follow-up assessments (repetition test battery) will take place directly after the intervention period and 6 months post-treatment. Study population/ datasources Study sample: patients hospitalized or attending day-treatment or receiving outpatient care at one of the participating centers. To maximize engagement, group therapy will be incorporated in the day program. Individual therapy sessions will be delivered flexibly (time, location). All participants are embedded within a low-threshold intensive outreaching care system (aligned with our academic department).

    6. Conditions and Keywords

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

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    The present study entails a single-blind two-level RCT directed at patients with recent onset schizophrenia. Participants are randomly assigned to intervention condition (Cognitive Behavioral Therapy- Social Activation (CBTsa) plus Standard Treatment (ST)), or to the control condition (ST alone). A baseline test battery is employed to examine causes of social withdrawal and interaction with treatment outcome. Follow-up assessments (repetition test battery) will take place directly after the intervention period and 6 months post-treatment.
    Masking
    ParticipantInvestigatorOutcomes Assessor
    Masking Description
    Randomisation is coordinated a staff member of the psychosis department who is not involved in the research team and not familiar with both the assessments or intervention procedure. The results of the randomization is concealed from the assessors. Every effort has been made to keep assessors blind to treatment condition, using the following strategies: research workers were not involved in the randomization process, therapists and research workers made use of different (secured) agendas, and work locations / rooms in order tot minimize the chance of potential blind breaks; patients will be frequently reminded by assessors not to talk about treatment allocation.
    Allocation
    Randomized
    Enrollment
    98 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    CBT-SA
    Arm Type
    Experimental
    Arm Description
    Group sessions for 4 weeks, two sessions per week, 60 minutes per session, two trainers (a CBT therapist and a CBT assistant); eight participants, and; Individual sessions (crystallizing learned skills, focus on individual needs) during 6-8 weeks, one session per week, 45 minutes per session
    Arm Title
    Standard Treatment
    Arm Type
    Active Comparator
    Arm Description
    Participants in both study conditions will receive ST. Participants are hospitalized or attending day-treatment at the Department of Early Psychosis, Amsterdam, the psychosis department of the ABC team, Utrecht, Parnassia Den Haag and collaborating (local community) mental health centers.
    Intervention Type
    Behavioral
    Intervention Name(s)
    CBT-SA
    Intervention Description
    Info has been included in arm description
    Intervention Type
    Behavioral
    Intervention Name(s)
    Standard Treatment
    Intervention Description
    Info has been included in arm description
    Primary Outcome Measure Information:
    Title
    Level of social engagement
    Description
    Level of social engagement as measured by experiences sampling method
    Time Frame
    3 months (at study completion)
    Title
    Negative symptoms
    Description
    Negative symptoms as measured with PANSS
    Time Frame
    3 months (at study completion)
    Title
    Negative symptoms
    Description
    Negative symptoms as measured with BNSS
    Time Frame
    3 months (at study completion)
    Secondary Outcome Measure Information:
    Title
    Quality of Life
    Description
    Assessed with the AQoL
    Time Frame
    3 months (at study completion)
    Title
    Global functioning
    Description
    Assessed with the GAF
    Time Frame
    3 months (at study completion)
    Title
    Productivity losses
    Description
    Effects on ability to perform paid and unpaid work
    Time Frame
    3 months (at study completion)
    Title
    Positive and General Symptomatology
    Description
    As assessed with the PANSS
    Time Frame
    3 months (at study completion)
    Title
    Depression
    Description
    Depression as assessed with the Calgary Depression Scale for Schizophrenia
    Time Frame
    3 months (at study completion)
    Title
    Inhibition/ Activation
    Description
    Behavioural Inhibition/ Behavioural Activation Scales (BISBAS)
    Time Frame
    3 months (at study completion)
    Title
    Need for care
    Description
    Camberwell Assessment of Need
    Time Frame
    3 months (at study completion)

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    35 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: recent onset schizophrenia or related disorder (start antipsychotic medication <2 yr); Social withdrawal (> 3 moderate severity on the PANSS N4; Passive/apathic social withdrawal; range 0-7); Aged 18-35 years; Fluent in Dutch IQ>70; Able and willing to give informed consent Exclusion Criteria: Younger than eighteen years of age; No mastery of the Dutch language; Negative symptoms as a consequence of positive symptoms (e.g. withdrawal due to paranoid delusions). Positive symptoms as such are not an exclusion criterion; only when they are considered to be the primary cause of the negative symptoms, in which case CBT focused on positive symptoms or another type of intervention for positive symptoms is called for.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Lieuwe de Haan, Ph.D.
    Organizational Affiliation
    Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    23454550
    Citation
    Staring AB, Ter Huurne MA, van der Gaag M. Cognitive Behavioral Therapy for negative symptoms (CBT-n) in psychotic disorders: a pilot study. J Behav Ther Exp Psychiatry. 2013 Sep;44(3):300-6. doi: 10.1016/j.jbtep.2013.01.004. Epub 2013 Feb 1.
    Results Reference
    background
    PubMed Identifier
    21969420
    Citation
    Grant PM, Huh GA, Perivoliotis D, Stolar NM, Beck AT. Randomized trial to evaluate the efficacy of cognitive therapy for low-functioning patients with schizophrenia. Arch Gen Psychiatry. 2012 Feb;69(2):121-7. doi: 10.1001/archgenpsychiatry.2011.129. Epub 2011 Oct 3.
    Results Reference
    background
    PubMed Identifier
    22616617
    Citation
    Verma S, Subramaniam M, Abdin E, Poon LY, Chong SA. Symptomatic and functional remission in patients with first-episode psychosis. Acta Psychiatr Scand. 2012 Oct;126(4):282-9. doi: 10.1111/j.1600-0447.2012.01883.x. Epub 2012 May 23.
    Results Reference
    background
    PubMed Identifier
    30419038
    Citation
    Wijnen BFM, Pos K, Velthorst E, Schirmbeck F, Chan HY, de Haan L, van der Gaag M, Evers SMAA, Smit F. Economic evaluation of brief cognitive behavioural therapy for social activation in recent-onset psychosis. PLoS One. 2018 Nov 12;13(11):e0206236. doi: 10.1371/journal.pone.0206236. eCollection 2018.
    Results Reference
    derived

    Learn more about this trial

    Cognitive Behavioural Therapy- Social Functioning In Adolescence With Recent Onset Schizophrenia

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