Intermittent fasting – Short- and long-term laboratory, fatigue and quality of life changes in healthy volunteers
Not Applicable
Recruiting
- Conditions
- Healthy volunteers (no severe illnessess)
- Registration Number
- DRKS00025459
- Lead Sponsor
- Poliklinik für Frauengesundheit und Geburtshilfe der Universitätsmedizin Mainz
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 35
Inclusion Criteria
= 18 years of age
- Voluntary participation
- Written informed consent
- Ability to understand nature and effects of
the trial participation
Exclusion Criteria
- Body mass index <18kg/m2
- Weight loss of > 10% of body weight in the last 6 months
- Current or recent diet aimed at reducing weight
- Current or past eating disorders
- Acute medical conditions (including ulcus/gastritis)
- Chronic or acute heart, liver or kidney disease
- Diabetes mellitus type I
- Large surgical procedures in the last 6 months
- Pregnancy & breastfeeding period
- Participation in another interventional trial likely to interfere with the study outcome
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Short- and long-term changes in quality of life (WHO-5, SF-36 quetsionnaires) and fatigue (FACIT, FAS questionnaires)
- Secondary Outcome Measures
Name Time Method Short- and long-term laboratory changes reflecting the general health status (including fat metabolism, kidney and liver function, blood sugars etc.)