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Behavioral & neurocognitive bases of social interactio

Conditions
Autism spectrum disorder
F40.1
F20
F42
Schizophrenia
Social phobias
Obsessive-compulsive disorder
Registration Number
DRKS00030741
Lead Sponsor
Institut für klinische Neurowissenschaften und medizinische Psychologie, Heinrich-Heine-Universität Düsseldorf
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
300
Inclusion Criteria

4 groups of patients / participants which fulfill following criteria:
- Healthy controls (n = 60)
- ASD patients as diagnosed based on ADOS-2/ADI-R and a clinical assessment by a qualified psychiatrist (n = 60).
- SCZ patients as diagnosed based on a clinical assessment by a qualified psychiatrist (n = 60)
- SAD patients as diagnosed on a clinical assessment by a qualified psychiatrist (n = 60).
- OCD patients as diagnosed on a clinical assessment by a qualified psychiatrist (n = 60).
- Ability to understand the study procedure
- Informed consent: A declaration of informed consent has to be signed and personally dated by the subject.

Exclusion Criteria

- Presence of disorders other than ASD, SCZ, SAD and OCD, which may deteriorate social functioning, motor function or cognitive abilities such as dementia, severe arthritis, drug/alcohol abuse, Alzheimer’s Disease, or stroke. However, because of high co-occurrence rate of conditions such as depressive disorders in ASD, SCZ, SAD and OCD, such disorders will be controlled for in the analyses but will not constitute a hard exclusion criterion. We will, however, attempt to recruit mainly individuals with no comorbidities.
- Inability to remain motionless in the fMRI scanner without involuntary movements providing intolerable artifacts
- Inability to give informed consent
- Claustrophobia
- Pregnancy
- MRI incompatible implants, such as cardiac pacemakers or magnetic objects
- Permanent makeup
- Large tattoos particularly in or near the imaging area
Abandon criteria:
- Occurrence of any exclusion criterion either at the time of recruitment or revealed after/during measurement such as incidental findings in the MRI images
- The patient’s / participant’s decision to abandon the study at any time
- Withdrawal of consent

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Parameter differences in motion tracking
Secondary Outcome Measures
NameTimeMethod
Brain function differences in fMRI and differences in tracking app activity logs
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