Obesity Clinical Trial
Official title:
The Use of a Probiotic Blend in Reducing Anthropometric Measurements and Improving Biochemical Parameters in Adults With Overweight and/or Obese
It is already known that dysbiosis, that is, qualitative and quantitative changes in the composition of the intestinal microbiota, can be associated with the development of a series of intestinal and extra-intestinal disorders. Dysbiosis is reported in irritable bowel syndrome, inflammatory bowel disease, colorectal cancer, allergic diseases, non-alcoholic steatohepatitis, arteriosclerotic diseases, neurological diseases and metabolic syndromes, mainly diabetes and obesity. Among the many factors that play a key role in obesity, a number of studies show the intestinal microbiota as an important contributor. Many studies carried out with probiotics have shown that their administration can be effective in the prevention and treatment of obesity. Furthermore, it is found that benefits for body weight, abdominal adiposity, anthropometric measurements and body composition are often associated with favorable metabolic effects.
Status | Recruiting |
Enrollment | 108 |
Est. completion date | December 30, 2023 |
Est. primary completion date | February 19, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: - Provision of Free and Informed Consent in writing, signed and dated; - Age according to the indicated population (18-65 years old) - both genders; - Body mass index (BMI) of 25 - 35 Kg/m2. Exclusion Criteria: - Pregnant and lactating women - Individuals with a history of daily consumption of probiotics, fermented milk and/or yogurt; subjects known to have demonstrated a prior reaction, including anaphylaxis, to any substance in the composition of the study product; - Individuals with concomitant participation in another clinical trial; - History of autoimmune, cardiovascular, thyroid, or chronic liver disease; - Making use of medication capable of affecting weight change, antidiabetic medication, hypolipidemic agents; - Individuals who have undergone weight loss surgery, - Weight change greater than 5% in the last three months. |
Country | Name | City | State |
---|---|---|---|
Brazil | Universidade do Extremo Sul Catarinense | Criciúma | Santa Catarina |
Lead Sponsor | Collaborator |
---|---|
Universidade do Extremo Sul Catarinense - Unidade Academica de Ciecias da Saude |
Brazil,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Body fat composition by Bioelectrical impedance analysis | By Bioelectrical impedance analysis (BIA). This is a method for estimating body composition, in particular body fat and muscle mass, where a weak electric current flows through the body and the voltage is measured in order to calculate impedance (resistance) of the body. | three months | |
Secondary | Total cholesterol by blood analyses | biochemical analyses before and after inclusion: Total cholesterol to be carried out in a reference laboratory. Total cholesterol will be measured in mg/dL | three months | |
Secondary | quality of life questionnaire score | quality of life and improvement of gastrointestinal symptoms by SF-36 scale (It comprises 36 questions that cover eight domains of health) | three months | |
Secondary | Gastrointestinal Symptom Rating Scale (GSRS) questionnaire score | GSRS scale: An interview-based rating scale consisting of 15 items for assessment of gastrointestinal symptoms | three months | |
Secondary | Weight | weight will be measured in kilograms | three months | |
Secondary | height | height will be measured in centimeters | three months | |
Secondary | HDL levels by blood analyses | biochemical analyses before and after inclusion: HDL to be carried out in a reference laboratory. HDL will be measured in mg/dL | three months | |
Secondary | LDL levels by blood analyses | biochemical analyses before and after inclusion: LDL to be carried out in a reference laboratory. LDL will be measured in mg/dL | three months | |
Secondary | triglycerides levels by blood analyses | biochemical analyses before and after inclusion: triglycerides to be carried out in a reference laboratory. triglycerides will be measured in ml/dL | three months | |
Secondary | Glucose levels by blood analyses | biochemical analyses before and after inclusion: glucose to be carried out in a reference laboratory. glucose will be measured in mg/dL | three months |
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