Clinical study of Vibrance therapeutic water on digestive health, stress reduction, and glucose level control.
- Conditions
- Health Condition 1: K929- Disease of digestive system, unspecified
- Registration Number
- CTRI/2024/08/072329
- Lead Sponsor
- Mystic Kingdom Pvt. Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Participants meeting all the following criteria will be eligible for the study:
1. Male and female participants aged 21-50 years (both inclusive); 2. BMI between 18.5 – 29.9 kg/m2; 3. Participants should self-report at least two of the following gastrointestinal symptoms: epigastric discomfort, heartburn, bloating, nausea, fullness in the stomach, abdominal pain, or anorexia; 4. Suffering from self-reported mild to moderate stress on the PSS scale score less than or equal to 26; 5. Participants must demonstrate their willingness to participate in the study and comply with its procedures by signing a written informed consent. 6. Subjects with or without type 2 diabetes, if diabetic should be on stable medication for at least the past 3 months and have HbA1c NMT 7.5%.(10 subjects will be enrolled which will be having type 2 diabetes)
Participants meeting any of the following criteria will not be eligible for the study:
1. Participants with major abdominal surgery, a history of inflammatory bowel disease or diverticular disease, celiac disease, allergic diseases, including asthma, psychiatric disorders and critical systemic illness as assessed by medical history, appropriate consultations and/or laboratory tests; 2. Actively having a gut infection; 3. History of or complications from malignant tumors; 4. Participant using or had used any probiotics, prebiotics herbs, dietary, nutraceutical, ayurvedic supplements or any other medicines for the digestive health, stress or glycemic control; 5. Females who are pregnant and have a positive urine pregnancy test/planning to be pregnant/lactating or not using reliable methods of contraception; 6. Participants with heavy alcohol consumption or smoking/tobacco consumption; 7. Participation in any other clinical study within the past 3 months or ongoing; 8. Any other reason that, in the opinion of the investigator, excludes the participant from eligibility for study participation.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method