healthy adults
Conditions
Interventions
Group 1: try compress and warm water compress
single application on breast
application time 30 minutes plus 30 minutes resting period after application
Group 2: ginger compress
application time 30 minutes plus 30 minutes resting period after application
Group 3: mustard flour compress
application time 10-15 minutes plus 30 minutes resting period after application
Sponsors
Charité Universitätsmedizin
Eligibility
Sex/Gender
All
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: - Age: 18 to 40 - no physical or mental disease - written consent
Exclusion criteria
Exclusion criteria: - severe physical and/or mental disease - known hypersensitivity towards the used substances - highly sensitive Skin - contact allergies or atopies - skin alterations or states of health that may affect the participation - participation in other trials if this affects the participation in this trial
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcomes are physiological changes measured via 24-hour ECG, peripheral and central body temperature, respiratory frequency and rhythm before and after the intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| Further outcomes are subjective sensations measured via psychometric tests and visual analog scales before and after the intervention as well as phenomenological interviews after the intervention | — |
Countries
Germany
Contacts
Public ContactWiebke Stritter
Charité Universitätsmedizin
Outcome results
None listed