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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05821660
Other study ID # F-2023-014
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 1, 2023
Est. completion date November 2023

Study information

Verified date August 2023
Source Buchinger Wilhelmi Development & Holding GmbH
Contact Buchinger Wilhelmi Clinic
Phone +49-7551-8070
Email forschung@buchinger-wilhelmi.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to assess changes in body and metabolism caused by this new five-day hypocaloric and ketogenic programme


Description:

Therapeutic effects of fasting are increasingly documented. Recent studies on a cohort of subjects doing a long-term fasting lasting from 4 days to several weeks demonstrated beneficial effects on health and well-being. In recent studies on the therapeutic efficacy of the Buchinger Wilhelmi fasting program, long-term fasting significantly improved risk factors for a variety of chronic diseases including hypertension even in medicated subjects, liver steatosis, inflammation, oxidative stress and lipoprotein distribution. There is an increasing demand for dietary interventions which can be delivered at home. This has been amplified by the Coronavirus-19 disease (COVID-19) pandemic during which many countries kept their population in lockdown at home in isolation. The COVID-19 pandemic has also influenced the lifestyle of individuals, with an increased consumption of unhealthy food and a sedentary behaviour resulting in mental (anxiety, depression, and others) and physical (weight gain, rise in blood pressure) health issues. In order to adapt to this new context, the Buchinger Wilhelmi Clinics have created a hypocaloric, ketogenic program with interval fasting. The five-day programme is designed to be easily integrated into everyday life and can be applied several times a year. The programme is based on ready-to-eat soups made with locally sourced organic ingredients. The ingredients represent a total daily intake of around 600 kcal per day - with a high share of fats and a limited quantity of carbohydrates and proteins. Minerals and micronutrients used at the Buchinger Wilhelmi Clinics are also supplied. Although the comprehensive medical care and assistance offered at the clinics cannot be replicated, medical professionals are available to support the customers remotely. The investigators hypothesise that the metabolic changes caused by this new five-day programme can be similar to a short-term fast. In order to test this hypothesis, the investigators will perform a two-arm randomized controlled trial in which a group of participants will perform the five-day Fastingbox programme and a group of participants will receive an eucaloric diet as a control group.


Recruitment information / eligibility

Status Recruiting
Enrollment 64
Est. completion date November 2023
Est. primary completion date September 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Exclusion Criteria: - Not able to sign the informed consent - diagnosticated with cachexia, anorexia, nervosa, advanced kidney, liver or cerebrovascular insufficiency. - Intake of antibiotics up to 2 months prior the study - Medicated high blood pressure - Diagnosed hyperuricemia - Diagnosed diabetes mellitus type I and II - Diagnosed kidney stone - Active malignant diseases - Known substance addiction - Pregnancy or breastfeeding - Participation in another study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Five-day hypocaloric and ketogenic programme
Dietary intervention

Locations

Country Name City State
Germany Buchinger Wilhelmi Clinic Überlingen Baden-Württemberg

Sponsors (5)

Lead Sponsor Collaborator
Buchinger Wilhelmi Development & Holding GmbH Buchinger Wilhelmi Clinic, King's College London, MVZ Labor Ravensburg GbR, Synlab Málaga

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Other Changes in body mass index in kg/m² through study completion (11 subsequent days as well as one month afterwards)
Other Changes in abdominal circumference in cm through study completion (11 subsequent days as well as one month afterwards)
Other Changes in resting heart frequency in beats/min through study completion (11 subsequent days as well as one month afterwards)
Other Changes in leucocytes measured in serum by a routine technique (electronic count) At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in erythrocytes measured in serum by a routine technique (electronic count) At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in haemoglobin measured in serum by a routine technique (photometry) At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in haematocrit measured in serum by a routine technique (electronic count) At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in MCV measured in serum by a routine technique (ELISA) At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in MCH measured in serum by a routine technique At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in MCHC measured in serum by a routine technique At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in thrombocytes measured in serum by a routine technique (electronic count) At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in INR measured in serum by a routine technique (coagulometry) in sec At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in PTT measured in serum by a routine technique (coagulometry) in sec At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in kidney parameters blood parameters: uric acid, urea, creatinine in mg/dl At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in uric acid measured in serum by a routine technique (enzymatic/uricase/peroxidas) in mg/dl At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in urea measured in serum by a routine technique (GLDH) in mg/dl At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in creatinine measured in serum by a routine technique (creatininase) in mg/dl At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in GOT measured in serum by a routine technique (IFCC method) in U/l At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in GPT measured in serum by a routine technique (IFCC method) in U/l At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in GGT measured in serum by a routine technique (IFCC modified) in U/l At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in AP measured in serum by a routine technique in U/l At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in sodium measured in serum by a routine technique (potentiometric, ISE) in mmol/l At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in potassium measured in serum by a routine technique (potentiometric, ISE) in mmol/l At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in calcium measured in serum by a routine technique (CPC) in mmol/l At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in magnesium measured in serum by a routine technique (ICPMS) in mmol/l At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in continous glucose monitoring glucose level in mg/dl At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in physical activity level questionnaires: International Physical Activity Questionnaire (IPAQ) 150min./week of exercise is considered sufficient physical activity At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in sleep quality questionnaires: Pittsburgh Sleep Quality Index (PSQI), score ranging from 0 to 21, where lower scores denote a healthier sleep quality At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in processed food consumption questionnaire: highly processed food consumption (sQ-HPF) At baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in physical well-being measured by visual scale (0-10) through study completion (11 subsequent days as well as one month afterwards)
Other Changes in emotional well-being measured by visual scale (0-10) through study completion (11 subsequent days as well as one month afterwards)
Other Changes in energy level measured by visual scale (0-10) through study completion (11 subsequent days as well as one month afterwards)
Other Changes in cravings measured by visual scale (0-10) through study completion (11 subsequent days as well as one month afterwards)
Other Changes in feeling bloated measured by visual scale (0-10) through study completion (11 subsequent days as well as one month afterwards)
Other Changes in feeling cold measured by visual scale (0-10) through study completion (11 subsequent days as well as one month afterwards)
Other Changes in tiredness measured by visual scale (0-10) through study completion (11 subsequent days as well as one month afterwards)
Other Changes in muscle weakness measured by visual scale (0-10) through study completion (11 subsequent days as well as one month afterwards)
Other Changes in back pain measured by visual scale (0-10) through study completion (11 subsequent days as well as one month afterwards)
Other Changes in headache measured by visual scale (0-10) through study completion (11 subsequent days as well as one month afterwards)
Other Changes in hunger measured by visual scale (0-10) through study completion (11 subsequent days as well as one month afterwards)
Other Changes in anxiety measured by visual scale (0-10) through study completion (11 subsequent days as well as one month afterwards9
Other Changes in digestive problems measured by visual scale (0-10) through study completion (11 subsequent days as well as one month afterwards)
Other Changes in optimism measured by visual scale (0-4) through study completion (11 subsequent days as well as one month afterwards)
Other Changes in relaxation measured by visual scale (0-4) through study completion (11 subsequent days as well as one month afterwards)
Other Changes in clear thinking measured by visual scale (0-4) through study completion (11 subsequent days as well as one month afterwards)
Other Changes in confidence measured by visual scale (0-4) through study completion (11 subsequent days as well as one month afterwards)
Other Changes in happiness measured by visual scale (0-4) through study completion (11 subsequent days as well as one month afterwards)
Other Changes in physical activity measured by visual scale (0-10) and absolut numbers through study completion (11 subsequent days as well as one month afterwards)
Other Ethnicity Caucasian, Hispanic, African American, Asian, others baseline
Other Smoking status: never, former, current, flatmate baseline
Other Alcohol consumption number of glasses: wine, beer, spirits baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in stress level measured by visual scale (0-10) baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in energy level measured by visual scale (0-10) baseline, after 5 and 9 days as well as 1 month afterwards
Other Changes in pain level measured by visual scale (0-10) baseline, after 5 and 9 days as well as 1 month afterwards
Primary Changes in body weight in kg through study completion (11 subsequent days as well as one month afterwards)
Primary Changes in systolic blood pressure in mmHg through study completion (11 subsequent days as well as one month afterwards)
Primary Changes in diastolic blood pressure in mmHg through study completion (11 subsequent days as well as one month afterwards)
Secondary Changes in acetoacetic acid measured by nitroprussid test in urine in mg/dL through study completion (11 subsequent days as well as one month afterwards)
Secondary Changes in total cholesterol measured in serum by a routine technique (photometry) At baseline, after 5 and 9 days as well as 1 month afterwards
Secondary Changes in HDL-C measured in serum by a routine technique (elimination/catalase) At baseline, after 5 and 9 days as well as 1 month afterwards
Secondary Changes in LDL-C measured in serum by a routine technique (elimination/catalase) At baseline, after 5 and 9 days as well as 1 month afterwards
Secondary Changes in triglycerides measured in serum by a routine technique (GPO, trinder without serum blank) in mmol/l At baseline, after 5 and 9 days as well as 1 month afterwards
Secondary Changes in glucose measured in serum by a routine technique (hexokinase) in mmol/l At baseline, after 5 and 9 days as well as 1 month afterwards
Secondary Changes in HbA1c measured in serum by a routine technique (HPLC) in % At baseline, after 5 and 9 days as well as 1 month afterwards
Secondary Changes in Insulin measured in serum by a routine technique (CLIA) in mU/l At baseline, after 5 and 9 days as well as 1 month afterwards
Secondary Changes in total antioxidant capacity measured in serum by a routine technique At baseline, after 5 and 9 days as well as 1 month afterwards
Secondary Changes in lipidperoxidation measured in serum by a routine technique (in µmol/l) At baseline, after 5 and 9 days as well as 1 month afterwards
Secondary Changes in well-being WHO-5 well-being index through study completion (11 subsequent days as well as one month afterwards)
Secondary Changes in ESR measured in mm/h by kinetic flow analysis in capillaries on a photometric basis At baseline, after 5 and 9 days as well as 1 month afterwards
Secondary Changes in CRP measured in serum by a routine technique At baseline, after 5 and 9 days as well as 1 month afterwards
Secondary Changes in IL-6 measured in serum by a routine technique (ECLIA) At baseline, after 5 and 9 days as well as 1 month afterwards
Secondary Changes in IL-10 measured in serum by a routine technique At baseline, after 5 and 9 days as well as 1 month afterwards
Secondary Changes in TNF-a measured in serum by a routine technique (CLIA) At baseline, after 5 and 9 days as well as 1 month afterwards
Secondary Changes in gut microbiome composition Shotgun metagenomics, qPCR, SCFA At baseline, first stool after 9 days as well as 1 month afterwards
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