Benefits of Combining MCT With CR in the Recovery of Patients With Psychotic Spectrum Disorders
Launched by UNIVERSITAT AUTONOMA DE BARCELONA · May 16, 2024
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is investigating whether a combination of two therapies, called REHACOP and Metacognitive Training (MCT), can help people with certain mental health conditions, like schizophrenia and related disorders, recover better than MCT alone. The researchers want to find out if this combined therapy improves not just clinical recovery, which means feeling better from symptoms, but also personal and social recovery. They’ll be looking at how well individuals think and interact with others, and whether the effects of the treatment last over time.
To participate, individuals must meet specific criteria, such as being diagnosed with one of the targeted psychotic disorders and being stable enough not to have needed hospitalization in the last three months. Participants will attend either eight or twelve weekly therapy sessions, depending on which group they are in, and will complete some self-assessments to track their progress. This study is currently recruiting participants of all genders, aged between 18 and 65, who are willing to join and give informed consent.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Presence of one of the e following diagnostics according to the criteria of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5): schizophrenia, schizophreniform disorder, delusional disorder, brief psychotic disorder, schizoaffective disorder, and non specified schizophrenia spectrum disorder and other psychotic disorders.
- • Be in a stable clinical phase (without psychiatric hospitalization in the last 3 months).
- • Have good adherence to pharmacological treatment.
- • T-score \< 40 in any cognitive outcome measured by TAVEC, CPT-IP, TMT, Stroop, WSCT, FAS and WAIS (Vocabulary, Digit Forward, Digit Backwards and Digit Symbol Coding.
- • Willing to participate in the study expressed by providing signed informed consent.
- Exclusion Criteria:
- • Presence of traumatic brain lesion, dementia or intellectual discapacity (IQ \<70).
- • Positive and Negative Syndrome Scale (PANSS) score \>= 5 in hostility and lack of cooperation and \>= 6 in suspiciousness.
- • Presence of an additional diagnosis of severe disorder related to substances.
- • Having participated in a CR and/or MCT intervention in the year prior to incorporation into the study.
About Universitat Autonoma De Barcelona
The Universitat Autònoma de Barcelona (UAB) is a prestigious academic institution located in Spain, renowned for its commitment to research and innovation in various fields, including healthcare and life sciences. As a clinical trial sponsor, UAB leverages its extensive resources and expertise to advance medical knowledge and improve patient outcomes through rigorous scientific investigation. The university fosters collaboration among multidisciplinary teams, ensuring that clinical trials are conducted with the highest standards of ethical practice and scientific integrity. UAB's dedication to education, research excellence, and community engagement positions it as a leading institution in the advancement of public health and medical research.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Cerdanyola Del Vallès, Barcelona, Spain
Patients applied
Trial Officials
Ana Barajas Velez
Principal Investigator
Universitat Autonoma de Barcelona
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported