Observational Study on the Safety, Health Improvement and Well-being of a Prolonged Fasting
Recruiting
- Conditions
- Prevention in healthy subjectsE66I10E88.9ObesityEssential (primary) hypertensionMetabolic disorder, unspecified
- Registration Number
- DRKS00021023
- Lead Sponsor
- Clínica Buchinger Wilhelmi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 1000
Inclusion Criteria
1. Age 18-90 years
2. beginning inpatient treatment or hospital stay (first 24 h) at the Clínica Buchinger Wilhelmi in Marbella
3. present written declaration of consent
Exclusion Criteria
1. no adequate linguistic communication possible
2. dementia or other cognitive impairment
3. existing pregnancy or breastfeeding period
4. participation in another study
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method therapeutic and preventive efficiency regarding:<br>- risk<br>-blood parameters (at the beginning and the end of the therapy)<br>- drug intake<br>- weight reduction and maintainance (daily during the inpatient stay and until 11 months afterwards by survey)<br>- reduction of the waist circumference<br>- blood pressure lowering (daily during the inpatient stay and until 11 months afterwards by survey)<br>- behavioral factors before and up to 11 months afterwards by survey<br>- general subjective well-being<br>- documentation of the diagnosis at the beginning of the stay
- Secondary Outcome Measures
Name Time Method Safety of the Buchinger Wilhelmi Program:<br>- documentation of disorders and fasting crises during the inpatient stay<br>- effects that possibly stay in relation with the therapy are documented by survey up to 11 months afterwards<br>- well-being: visual scalas to capture the physical and emotional well-being daily during the stay<br>- documentation of the quality of life before and up to 11 months afterwards by survey