Investigation of the natural variance of human time experience
- Conditions
- F84.5F31F32F20Asperger syndromeBipolar affective disorderDepressive episodeSchizophrenia
- Registration Number
- DRKS00020493
- Lead Sponsor
- Forschungszentrum Jülich GmbH Institut für Neurowissenschaften und Medizin (INM-3) Kognitive Neurowissenschaft
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 360
For healthy subjects:
-Clinical and anamnestic exclusion from neurological and mental disorders.
-No current psychotropic medication.
-Age between 18 and 55 years.
-Normal or corrected vision.
-Legally effective, written consent form of the subject to participation in the study.
For groups with diagnosis F84.5 (ASS):
-Diagnosed with Asperger's-Syndrome (F84.5) according to the ICD-10.
-Clinical and anamnestic exclusion from comorbid neurological and mental disorders.
-No current psychotropic medication.
-Age between 18 and 55 years.
-Normal or corrected vision.
-Legally effective, written consent form of the subject to participation in the study.
For groups with diagnosis F31 or F32 (Depression): -Diagnosed with Depression (F31 or F32) according to the ICD-10.
-Clinical and anamnestic exclusion from comorbid neurological and mental disorders.
-Age between 18 and 55 years.
-Normal or corrected vision.
-Legally effective, written consent form of the subject to participation in the study.
For groups with diagnosis F20 (Schizophrenia). -Diagnosed with Schizophrenia (F20) according to the ICD-10.
-Clinical and anamnestic exclusion from comorbid neurological and mental disorders.
-Age between 18 and 55 years.
-Normal or corrected vision.
-Legally effective, written consent form of the subject to participation in the study.
Exclusion Criteria for healthy subjects:
-Minors and people older than 55 years.
-Current or preceding diagnosis of a mental or neurological disorder.
-Existent internal ailments (malignant tumors, HIV-infection: no HIV-tests will be carried out.)
-Known MRI- or EEG-abnormalities.
-Acute suicidal tendency, risk of self-harm or harm to others.
-Missing legally effective, written consent form of subjects to participation in the study, people not qualified for legal acts or those in governmental or judicial custody (PsychKG, BTG).
Exclusion Criteria for patients with Asperger's-Syndrome (F84.5):
-Minors and people older than 55 years.
-Current or preceding diagnosis of a mental or neurological disorder, but not F84.5.
-Existent internal ailments (malignant tumors, HIV-infection: no HIV-tests will be carried out.)
-Known MRI- or EEG-abnormalities.
-Acute suicidal tendency, risk of self-harm or harm to others.
-Missing legally effective, written consent form of subjects to participation in the study, people not qualified for legal acts or those in governmental or judicial custody (PsychKG, BTG).
Exclusion Criteria for patients with Depression (F31 & F32):
-Minors and people older than 55 years.
-Current or preceding diagnosis of a mental or neurological disorder, but not F31 or F32.
-Existent internal ailments (malignant tumors, HIV-infection: no HIV-tests will be carried out.)
-Known MRI- or EEG-abnormalities.
-Acute suicidal tendency, risk of self-harm or harm to others.
-Missing legally effective, written consent form of subjects to participation in the study, people not qualified for legal acts or those in governmental or judicial custody (PsychKG, BTG).
Exclusion Criteria for patients with Schizoprenia (F20.x):
-Minors and people older than 55 years.
-Current or preceding diagnosis of a mental or neurological disorder, but not F20.x.
-Existent internal ailments (malignant tumors, HIV-infection: no HIV-tests will be carried out.)
-Known MRI- or EEG-abnormalities.
-Acute suicidal tendency, risk of self-harm or harm to others.
-Missing legally effective, written consent form of subjects to participation in the study, people not qualified for legal acts or those in governmental or judicial custody (PsychKG, BTG).
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Goal is the examination of human time perception (duration and passage of time) and the influence of various environmental factors.
- Secondary Outcome Measures
Name Time Method