Treatment-resistant Schizophrenia Clinical Trial
Official title:
A Pilot Randomized Controlled Study to Compare Avatar Therapy and Cognitive Behavioral Therapy in Patients With Treatment-resistant Schizophrenia.
Verified date | July 2020 |
Source | Ciusss de L'Est de l'Île de Montréal |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Schizophrenia is associated with long-lasting health, social and financial burden for patients, families, caregivers and society. Unfortunately, 25-30% of schizophrenia patients respond poorly to antipsychotic medication. Moreover, psychotherapeutic treatment alternatives are very limited for this suffering population. This unmet clinical need requires innovation and action. Psychotherapeutic treatment alternatives such as Cognitive Behavior Therapy (CBT) provide at best moderate results. Using immersive virtual reality, we recently tested a novel psychotherapeutic intervention, Avatar Therapy (AT), where the therapist engages in a dialogue with the patient through a virtual representation of the patient's distressing voice. This approach, being both relational and experiential, provides a unique opportunity to aid patients gain control over their voice. The results of our pilot study on AT were clinically promising for the severity and distress related to hallucinations, positive symptomatology and emotion regulation. To further research in this field, the primary goal of this randomized-controlled, single-site parallel study is to show that AT is superior to CBT for the treatment of persistent auditory hallucinations in schizophrenia. Our secondary goal is to examine the effects of these interventions on emotion regulation, mood symptoms (anxiety and depression), self-esteem, level of functioning and quality of life.
Status | Completed |
Enrollment | 74 |
Est. completion date | July 1, 2020 |
Est. primary completion date | March 31, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - distressing auditory verbal hallucinations - medication resistance relating to auditory verbal hallucinations (no response after 3 antipsychotics trials lasting at least 4 weeks each with a minimum of 400mg chlorpromazine equivalent) - DSM-5 diagnosis of schizophrenia or schizoaffective disorder Exclusion Criteria: - any change in medication within the past 2 months; - substance use disorder within the last 12 months - neurological disorder or unstable and serious physical illness - ongoing psychotic episode - Cognitive Behavioral Therapy for psychosis within the last 12 months |
Country | Name | City | State |
---|---|---|---|
Canada | Institut Universitaire en Santé Mentale de Montréal | Montréal | Quebec |
Lead Sponsor | Collaborator |
---|---|
Ciusss de L'Est de l'Île de Montréal | Otsuka Canada Pharmaceutical Inc. |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Change in Igroup Presence Questionnaire (IPQ) | 14-item scale measuring the sense of presence; Range 0-84, Higher values indicate a stronger feeling of presence | At the end of each Avatar Therapy session | |
Primary | Change in Psychotic Symptom Rating Scale (PSYRATS) - auditory hallucinations | 11-item structured interview assessing the severity of auditory hallucinations; Range 0-44, Higher values indicate a worse outcome | Within 1 week before treatment, within 1 week after treatment, follow-ups at 3 months, 6 months and 12 months | |
Secondary | Change in Beliefs About Voices Questionnaire - Revised (BAVQ-R) | 35-item self-reported measure designed to assess key beliefs and responses people have concerning their voice; Range 0-105, Higher scores indicate more beliefs and responses toward their voice | Within 1 week before treatment, within 1 week after treatment, follow-ups at 3 months, 6 months and 12 months | |
Secondary | Change in Positive And Negative Syndrome Scale (PANSS) | 30-item semi-structured interview investigating overall symptoms severity of schizophrenia in the last week; Range 30-210, Higher values indicate a more severe symptomatology | Within 1 week before treatment, within 1 week after treatment, follow-ups at 3 months, 6 months and 12 months | |
Secondary | Change in Beck Depression Inventory - II (BDI-II) | 21-item self-reported measure assessing depression symptoms over the past 2 weeks; Range 0-63, Higher values indicate more severe depressive symptomatology | Within 1 week before treatment, within 1 week after treatment, follow-ups at 3 months, 6 months and 12 months | |
Secondary | Change in Quality of Life Enjoyment and Satisfaction Questionnaire - Short Form (QLESQ-SF) | 16-item self-reported scale measuring enjoyment and satisfaction experienced during the past week in various areas of daily functioning; Range 14-70, Higher values indicate a better satisfaction of life | Within 1 week before treatment, within 1 week after treatment, follow-ups at 3 months, 6 months and 12 months | |
Secondary | Change in Empowerment scale (Making Decisions) - Revised Short Form | 25-item self-reported scale measuring the feeling of empowerment; Range 25-100, Higher values indicate a stronger feeling of empowerment | Within 1 week before treatment, within 1 week after treatment, follow-ups at 3 months, 6 months and 12 months |
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