Probiotic Yogurt Impact on Gut Health and Microbiota in Healthy Adults
yogurt intervention
Supportive Care Study
Summary
Study start date: March 9, 2021
Actual date on which the first participant was enrolled.The study investigates the effects of a special yogurt containing probiotics on gut health in adults aged 20-65 who are generally healthy and not currently dealing with digestive issues. The goal is to see how this yogurt impacts bowel movements and the types of bacteria in the gut. Participants are asked to avoid other probiotic foods or supplements during the study period, making it easier to attribute any changes to the yogurt being tested. This research is important because understanding how probiotics can benefit gut health could lead to better dietary recommendations for maintaining a healthy digestive system. Participants start with a 2-week adaptation period before being randomly assigned to consume either the probiotic yogurt or a regular dairy product twice daily for 4 weeks. Researchers collect various health measurements, such as body weight and blood markers, at the beginning and end of the study. Participants also keep a food diary and report on their bowel movement patterns. Stool samples are taken to analyze the types of bacteria present, using advanced genetic sequencing techniques. This helps determine how the probiotics in the yogurt might influence gut bacteria composition, which is crucial for understanding its potential health benefits.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.22 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 20 to 65 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
50% chance of being blinded to the placebo group
Treatment Groups
Group I
PlaceboGroup II
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location