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Controlled prospective study to evaluate the inpatient naturopathic fasting therapy in overweight and obese patients

Not Applicable
Conditions
E66
I10
I11
E78
R63.2
F50.4
Obesity
Essential (primary) hypertension
Hypertensive heart disease
Disorders of lipoprotein metabolism and other lipidaemias
Registration Number
DRKS00006343
Lead Sponsor
Abt. für Naturheilkunde, Klinik Blankenstein
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
90
Inclusion Criteria

Patients aged from 18 to 75 years, who were overweight (BMI 25-29.9 kg / m²) or obese (BMI = 30 kg / m²), wished to reduce body weight and who were prescribed fasting therapy or a weight reduction diet as a form of nutritional therapy and gave informed consent were included.

Exclusion Criteria

We excluded pregnant and lactating women and patients who participated in another study simultaneously or in an organized weight-reduction program or took a medicament against obesity. Further exclusion criteria were: condition after extensive bowel resection or bariatric treatment, inflammatory bowel disease, malignant neoplastic disease, postoperative nutritional deficit, hepatic or renal failure, insulin-dependent diabetes mellitus, not compensated hypothyroidism or hyperthyroidism, coronary heart disease or acute or chronic cardiac arrhythmia, eating disorders like anorexia nervosa, bulimia or binge-eating disorder, severe psychiatric disorders, addictive disorders and dementia.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The primary objective of the present study is the weight loss after 6 months of patients who received in-patient fasting treatment in comparison to those receiving a weight reduction diet. A mean difference of 3 kg between the treatment groups was considered clinically significant: A permanent reduction of 5% of the starting weight is considered a success and a general goal of therapy in both German and U.S. American guidelines.
Secondary Outcome Measures
NameTimeMethod
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