Social Cognition and Iron Dysregulation in Schizophrenia: A Longitudinal Study
This study aims to observe changes in your ability to understand others' mental states, attributional style, emotion recognition, and emotion regulation choice over time, if you are an individual diagnosed with schizophrenia.
Data Collection
Collected from today forward - ProspectiveSelf-Control+7
+ Behavior
+ Mental Disorders
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Summary
Study start date: September 1, 2026
Actual date on which the first participant was enrolled.This study focuses on understanding how schizophrenia impacts social thinking, emotion regulation, brain function, and biological processes over time. It involves two groups: individuals diagnosed with schizophrenia and healthy adults without schizophrenia. The goal is to compare how these aspects change in people with schizophrenia compared to healthy adults, which could help improve our understanding and care for this condition. The study also aims to explore how these changes differ from normal aging. Participants from both groups will complete a series of behavioral tasks and questionnaires at three different times: at the start of the study, after one year, and after two years. These tasks assess abilities such as understanding others, processing social information, and regulating emotions. For those with schizophrenia, clinical symptoms and their severity will also be assessed. Blood and hair samples will be collected at all visits to investigate biological factors related to mental health and stress. Participants will also undergo an MRI brain scan at the start and after one year. The study's outcomes include changes in the ability to understand others' mental states, attributional style, emotion recognition, and emotion regulation choice.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.180 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 70 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Department of Psychiatry, Psychotherapy, Psychosomatics and Medical Psychology; Medical University of Innsbruck
Innsbruck, AustriaOpen Department of Psychiatry, Psychotherapy, Psychosomatics and Medical Psychology; Medical University of Innsbruck in Google Maps