F98.5
Conditions
Interventions
Group 1: There are two experimental groups. The case group consists of stuttering patients. They provide in the context of the study a genetic sample, a handscan (to measure prenatal testosterone) and
Sponsors
Institut für Psychologie, Universität Bonn
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: The patient group must consist of persons who stutter. The control group consists of healthy participants.
Exclusion criteria
Exclusion criteria: A history of psychiatric / neurological disorder (exception stuttering in the patient group)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| One primary outcome of the study is reached after defining the role of dopaminergic/serotonergic polymorphisms for stuttering. A further primary outcome is to clarify the role of prenatal testosterone for stuttering (2D:4D study). A further primary endpoint is the investigation of the basal ganglia and its role in stuttering in the MRI study. | — |
Secondary
| Measure | Time frame |
|---|---|
| A secondary outcome is to produce new hypothesis on candidate genes for stuttering from the results of the experiments and MRI data. | — |
Countries
Germany
Contacts
Public ContactChristian Montag
Institut für Psychologie, Universität Bonn
Outcome results
None listed