Classical Conditioning of human neuroendocrine functions
Not Applicable
- Conditions
- healthy participants
- Registration Number
- DRKS00006750
- Lead Sponsor
- Klinik für Endokrinologie und Stoffwechselerkrankungen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Male
- Target Recruitment
- 34
Inclusion Criteria
healthy male non-smokers at the age of 18 to 40 years
Exclusion Criteria
immunological, endocrine, cardiovascular, hemic or psychiatric diseases, hightened BMI, allergy concerning during the study used substances, liver- oder kidney-disease, chronic obstructive lung disease, dependancy or diabetes mellitus
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method it will be measured ACTH in plasma, Cortisol in plasma, Cortisol in saliva: before the injection and 15, 30, 45, 60, 120 and 180 minutes after the injection
- Secondary Outcome Measures
Name Time Method Heartrate and pulse before the injection and 15, 30, 45, 60, 120 and 180 minutes after the injection<br>side effects and psychological parameters via standardized questionnaires about one week before and during the study at the same time points as mentioned above. <br>Following questionnaires were used: <br>SSAS, HADS, BIS/BAS, BMQ, PSQ, Adherence Scale Marburg, STAI-State, STAI-Trait, SWE, SFA-K, GASE-P. Additionally we asked for general frequency of side effects, estimation of probability of side effects and occurrence of specific side effects. We also asked for a estimation of the beverage concerning different dimensions. <br>