F90
Conditions
Interventions
Group 1: Adult patients with ADHD in whom the following parameters are assessed over a period of 14 complete days using two smartphone apps and an activity tracker (EmpaticaEmbrace Plus):
Initial ass
Sponsors
Klinik und Poliklinik für Psychiatrie und Psychotherapie Universitätsklinikum Bonn
Eligibility
Sex/Gender
All
Age
18 Years to 55 Years
Inclusion criteria
Inclusion criteria: The following inclusion criteria apply to the ADHD group: - Current diagnosis of ADHD according to DSM-V or ICD-10 - Age between 18-55 years - Use of an Android smartphone The following inclusion criteria apply to the control group - Age between 18-55 years - Use of an Android smartphone
Exclusion criteria
Exclusion criteria: The following exclusion criteria apply to the ADHD group: - Taking psychotropic medication (e.g. ADHD medication, antidepressants) - Use of antihypertensive medication or non-topically applied long-term medication - Seizure disorder (epilepsy) or other severe (neurological) illnesses or severe mental disorders such as schizophrenia - pregnancy The following exclusion criteria apply to the control group - mental disorders - No seizure disorders (epilepsy) or other serious (neurological) illnesses - Taking psychotropic medication (e.g. ADHD medication, antidepressants) - Use of antihypertensive medication or non-topically applied long-term medication - Pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| All endpoints are checked after 14 days of data collection a) - Heart rate, heart rate variability, steps, activity and movement data, sleep - collected via the Empatica EmbracePlus, aggregated data - data will be examined with regard to the differences between the groups (between-subject) and the time of day (within-subject) b) - Smartphone usage data and context data (number of screen locks, smartphone usage time, usage time for various app categories, brightness during simultaneous smartphone use, volume) - collected via smartphone app - data will be examined with regard to the differences between the groups (between-subject) and the time of day (within-subject) c) - EMA symptom intensity data are analyzed with regard to the differences between the groups (between-subject) and the time of day (within-subject) - collected via smartphone app d) - In addition, the parameters will be compared with regard to the differences in variance between the groups | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. The passively collected data will continue to be used to predict the symptom intensity collected via EMA at three times of day. 2. In addition, the data collected over the week will be used to predict the (psychopathological) constructs collected weekly 3. Further exploratory analyses, such as in-depth (among other things based on the raw data) evaluations of sleep data or physical activity data | — |
Countries
Germany
Contacts
Public ContactNiclas Braun
Klinik und Poliklinik für Psychiatrie und Psychotherapie Universitätsklinikum Bonn
Outcome results
None listed