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Effect of a plant extract containing dietary supplement on psychopathologic stress reactions among healthy participants

Not Applicable
Conditions
STRESSHealthy volunteers
Registration Number
DRKS00006008
Lead Sponsor
Schaper & Brümmer GmbH & Co. KG
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
65
Inclusion Criteria

• Age: 25-60 years
• Men and Women
• Non-smokers
• written consent after information about study contents and study procedure
• Ability and willingness of study participants to follow study leaders instructions

Exclusion Criteria

• severe chronic illness (manifest coronary heart disease, cancer, • insulin-dependent diabetes mellitus Typ I and II), severe kidney or liver diseases
•Psychological diseases (ADHS, Depression, panic, anxiety)
• food allergies, known endokrine and immunological diseases
• chronic gastroinestinal diseases (especially small intestine e.g. duodenal ulcer, liver, pancreas) and state after gastrointestinal surgical procedure e.g. nontropical sprue, short bowel syndrome), stomach stapling operations, gastric band
•oral mucositis, dental diseases, inflammation in the oral cavity
•Hormonal disorders, for example, hyperthyroidism and Cushing's syndrome
• heart surgery (Stent, Bypass, Heart pacemaker/ gastrointestinal surgery (not: elimination of appendix or gall bladder)
• • immediate planned surgery
• addiction to alcohol and/or drugs
•Pregnancy, lactation
•Smokers
•Persons with body mass index > 30
•Persons who are not able or not allowed to give written consent
•simultaneous participation at another clinical trial or participation within the last 30 days

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Stress tolerance (six weeks after first examination (t6) in comparison to first examination (t0)), respectivly measured as changes of the cognitive performance and visual attentnion under stress, using the Trail Making Test (TMT), before and after an acute stress impulse.
Secondary Outcome Measures
NameTimeMethod
•stress tolerance (six weeks after first examination (t6) in comparison to first examination (t0)), respectively measured by changes in the cognitive performance and visuell attention in the Colour Word Test (CWT) (Duration: 10 minutes) <br>•subjective stress perception (six weeks after first examination (t6) in comparison to first examination (t0)) (according to the Perceived Stress Questionnaire)<br>•acute subjective stress perception (six weeks after first examination (t6) in comparison to first examination (t0)) (according to General Stress Questionnaire) before and after an acute stress impulse.
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