Healthy participants will be analysed. Stress reduction
Conditions
Interventions
Group 1: Group I: Hypnosis and aroma participants in this group receive a 15-minute smartphone-based hypnotherapy intervention three times a week combined with the independent application of a specifi
Sponsors
Klinik für Pädiatrie mit Schwerpunkt Onkologie und Hämatologie Charité Universitätsmedizin Berlin
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Residence in Germany, use of your own smartphone or PC to use the relaxation sessions
Exclusion criteria
Exclusion criteria: Previous or concomitant mental illnesses now or in the last 3 years, active psychotherapy, active hypnotherapy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary endpoint: change in the perception of wakefulness-fatigue (subscale WM) and restlessness (subscale RU) of the Multidimensional Well-Being Questionnaire (MDBF) between group I and group II with a comparison of baseline and end-of-study values. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints: Follow-up comparison between groups I and III to assess the effectiveness of conditioning based on the change in the perception of wakefulness-fatigue and restlessness (subscale RU) of the Multidimensional Mood Questionnaire (MDBF). | — |
Countries
Germany
Contacts
Public ContactMartin Bogdanski
Klinik für Pädiatrie mit Schwerpunkt Onkologie und Hämatologie Charité Universitätsmedizin Berlin
Outcome results
None listed