Efficacy and Mechanisms of Change of an Emotion-oriented Version of Cognitive-behavioral Therapy for Psychosis (CBTd-E)

March 3, 2020 updated by: Prof. Dr. Stephanie Mehl, Philipps University Marburg Medical Center

Efficacy and Mechanisms of Change of an Emotion-oriented Version of Cognitive-behavioral Therapy for Psychosis (CBTp-E) in Reducing Delusions. A Randomized-controlled Treatment Study (CBTd-E)

The aim of the present single-blind randomized-controlled therapy study is to assess the efficacy of a new form of Cognitive Behavioral Therapy for delusions with a focus on emotion regulation, improvement of self-esteem and sleep quality (CBTd-E).

Study Overview

Detailed Description

Numerous meta-analyses have found Cognitive Behaviour Therapy for psychosis (CBTp) to be effective. The effect sizes that are achieved for positive symptoms in addition to antipsychotic treatment vary between small to medium. However, the effect sizes for changes in delusions are somewhat lower. Thus, it could prove beneficial to tailor CBTp interventions more precisely to the processes that are relevant to delusions. Empirically derived models of the formation and maintenance of delusions postulate an important role of cognitive biases, emotional factors and self-esteem. Additional studies have demonstrated the relevance of impaired sleep to delusions. Nevertheless, CBTp interventions that aim to change delusions tend to focus mainly on reasoning bias.

The results of several uncontrolled pilot studies that focused primarily at improving emotional factors, quality of sleep and self-esteem in patients with delusions indicate that changes in these factors have the potential to reduce delusions. However, in these studies the singular interventions were short and were not implemented into a broader therapy rational. It can thus be assumed that a combination of CBT-interventions within a broader therapy rational might have an even greater impact on delusions.

The aim of the present single-blind randomized-controlled therapy study is to assess the efficacy of a new form of Cognitive Behavioral Therapy for delusions with a focus on emotion regulation, improvement of self-esteem and sleep quality (CBTd-E) that will be applied in 25 individual sessions. Moreover, the study aims to test whether the efficacy of CBTd-E is mediated by the postulated processes. The main hypotheses are:

  1. Baseline differences: in comparison to healthy controls, patients with schizophrenia show more pronounced problems in emotion regulation, a reduced sleep quality and a lower and less stable self-esteem.
  2. Efficacy of CBTd-E: patients with acute delusions who receive CBTd-E show a more pronounced reduction of delusions (primary outcome), as well as a more pronounced reduction of positive symptoms, depression and general psychopathology, a stronger improvement in general and social functioning and will receive lower doses of antipsychotic medication (secondary outcomes) at post-treatment.
  3. Mediation: the effect of CBTd-E on change in delusions is mediated by a) improved emotional stability and ability to regulate one's own emotions, b) improved sleep quality, c) improved and more stable self-esteem.

In addition to questionnaires and interviews, behavioral paradigms, psychophysiological assessments and electronic diaries will be used to test the hypotheses. If we can demonstrate that CBTd-E reduces delusions, this would provide us with a more acceptable and feasible therapy for treating delusions.

Study Type

Interventional

Enrollment (Actual)

94

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Hamburg, Germany, 20146
        • University of Hamburg, Faculty of Clinical Psychology and Psychotherapy
    • Hessen
      • Marburg, Hessen, Germany, 35037
        • University of Marburg, Faculty of Clinical Psychology and Psychotherapy

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

14 years to 68 years (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Treatment Group:

Inclusion Criteria:

  • Diagnosis of schizophrenia, schizoaffective disorder, delusional disorder (DSM-5 diagnosis)
  • Delusions present in the last three months (score of at least three in three out of six PSYRATS scores)
  • problems in at least two out of three possible mediators: sleep problems (ISI sum score > 7), low self-esteem (score > 3in the BCSS negative self scale) and/or problems in emotion regulation (score in all items < 4)
  • fluent in German language
  • agree to participate
  • estimated general intelligence of at least 70 in the German Mehrfachwahlwortschatztest (MWT-B)
  • no present suicidality

Exclusion Criteria:

  • acute suicidal tendency
  • comorbid diagnosis of borderline personality disorder and/or substance use disorder in the last six month
  • taking of Benzodiazepines

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: CBTd-E
Experimental: emotion-oriented Cognitive Behavior Therapy focused on delusions for patients with schizophrenia-spectrum disorders and delusions. The therapeutical intervention follows a treatment-manual consisting of two modules. Patients work on two modules every week for 25 weeks in a row. Module I comprises psychoeducation on emotions, training radical acceptance of emotions and mindfulness, cognitive and behavioral strategies in order to change negative emotions and in order to foster positive emotions and suggestions for life-style changes (positive activities, sports, stress reduction). In the second module, the focus is on self-acceptance. Patients receive psychoeducation on self-acceptance and learn strategies in order to reduce negative self-schema and foster positive self-schema.
Emotion-oriented Cognitive Behavior Therapy with a focus on delusions: Aim of the intervention is to change factors that are involved in the formation and maintenance of delusions: emotional stability and regulation of negative emotions, sleep quality and self-esteem.
Other Names:
  • CBTd-E
Placebo Comparator: Treatment as Usual
Patients who are randomized and assigned to the Wait-list receive treatment as usual (regular visits to a physicist every third month and antipsychotic medication). After six month the waiting list patients receive the treatment specified above.
Emotion-oriented Cognitive Behavior Therapy with a focus on delusions: Aim of the intervention is to change factors that are involved in the formation and maintenance of delusions: emotional stability and regulation of negative emotions, sleep quality and self-esteem.
Other Names:
  • CBTd-E

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Psychotic Rating Scale (PSYRATS) delusions scale
Time Frame: Change between pre-therapy and post-therapy assessment after six month
Assessment of delusion frequency, delusion distress, conviction and loss of quality of life due to the delusion
Change between pre-therapy and post-therapy assessment after six month

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Positive and Negative Syndrome Scale (PANSS)
Time Frame: Change between pre-therapy and post-therapy assessment after six month
Assessment of positive, negative and general symptoms of schizophrenia
Change between pre-therapy and post-therapy assessment after six month
Change in Calgary Depression Rating Scale for Schizophrenia (CDSS(
Time Frame: Change between pre-therapy and post-therapy assessment after six month
Assessment of depressive symptoms in patients with schizophrenia
Change between pre-therapy and post-therapy assessment after six month
Change in Role Functioning Scale (RFS)
Time Frame: Change between pre-therapy and post-therapy assessment after six month
Assessment of social functioning
Change between pre-therapy and post-therapy assessment after six month
Change in Peters et al. Delusions Inventory (PDI- R)
Time Frame: Change between pre-therapy and post-therapy assessment after six month
Assessment of self-rated delusion frequency, conviction and distress.
Change between pre-therapy and post-therapy assessment after six month

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Emotion-regulation Questionnaire (ERQ)
Time Frame: Change between pre-therapy and post-therapy assessment after six month
Questionnaire assesses the regular use of emotion regulation strategies
Change between pre-therapy and post-therapy assessment after six month
Change in Emotion regulation inventory
Time Frame: Change between pre-therapy and post-therapy assessment after six month
Questionnaire assesses the regular use of emotion regulation strategies
Change between pre-therapy and post-therapy assessment after six month
Change in Paranoia assessed with Electronical mobile assessment
Time Frame: Change between pre-therapy and post-therapy assessment after six month
Assessment of present emotions, emotion regulation strategies, present symptoms of psychosis, present delusions, self-esteem for six consecutive days (10 assessments per day) in daily life
Change between pre-therapy and post-therapy assessment after six month
Change in Sleep quality as assessed with an Actiwatch
Time Frame: Change between pre-therapy and post-therapy assessment after six month
Assessment of sleep-quality using an electronic bracelet for six consecutive days, sleep quality is assessed with movement detectors and light sensors
Change between pre-therapy and post-therapy assessment after six month
Change in Emotion regulation quality as assessed experimental using International Affect Picture System Paradigm for the Assessment of emotion regulation (IAPS)
Time Frame: Change between pre-therapy and post-therapy assessment after six month
Assessment of effectiveness of use of emotion regulation strategies after experimental induction of fear, assessment of heart rate and skin conduction
Change between pre-therapy and post-therapy assessment after six month
Change in heart rate variability
Time Frame: Change between pre-therapy and post-therapy assessment after six month
Assessment of heart rate variability with sensors during stress induction (reaction experiment) and during rest
Change between pre-therapy and post-therapy assessment after six month
Change in Brief Core Schema Scale (BCSS)
Time Frame: Change between pre-therapy and post-therapy assessment after six month
Assessment of positive and negative self-schemata and schemata on others
Change between pre-therapy and post-therapy assessment after six month
Change in Insomnia Severity Index (ISI)
Time Frame: Change between pre-therapy and post-therapy assessment after six month
The ISI assesses present sleep problems
Change between pre-therapy and post-therapy assessment after six month
Change in Self-Compassion Scale (SCS)
Time Frame: Change between pre-therapy and post-therapy assessment after six month
SCS assesses self-compassion and self-esteem
Change between pre-therapy and post-therapy assessment after six month
Change in Self-perception of emotional competencies (SEK-27)
Time Frame: Change between pre-therapy and post-therapy assessment after six month
Questionnaire assesses the regular use of emotion regulation strategies
Change between pre-therapy and post-therapy assessment after six month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Stephanie Mehl, Ph. D., Philipps University Marburg Medical Center
  • Study Chair: Tania M Lincoln, Ph. D., University of Hamburg-Eppendorf
  • Principal Investigator: Tobias Teismann, Ph. D., Ruhr University of Bochum

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 1, 2016

Primary Completion (Actual)

December 31, 2019

Study Completion (Actual)

December 31, 2019

Study Registration Dates

First Submitted

February 26, 2016

First Submitted That Met QC Criteria

May 25, 2016

First Posted (Estimate)

June 1, 2016

Study Record Updates

Last Update Posted (Actual)

March 5, 2020

Last Update Submitted That Met QC Criteria

March 3, 2020

Last Verified

March 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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