Clinical Study of De-Stress & Happy Gut Powder for Stress and Indigestion in Adults.
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age21-50
SponsorHerbolab India Pvt. Ltd.
About this trial
The current study focuses on clinical validation of efficacy of nutraceutical product in relieving stress and functional dyspepsia symptoms in adults for gut health. The effect of these nutraceuticals not only targets the physical symptoms but also enhances overall well-being. Improved digestive health leads to better nutrient absorption, which is essential for energy levels and immune function. Reduced stress levels contribute to better sleep quality, cognitive function, and emotional stability.
Eligibility criteria
Qualifiers
Male and female participants aged 21-50 years both inclusive
Suffering from self-reported mild to moderate stress on the PSS scale score less than or equal to 26
Participants willing to participate in clinical trials and who have read understood and signed the informed consent form
No severe anxiety and depression i.e. Generalized anxiety disorder GAD score less than or equal to 10 and Patients' health questionnaire-9 PHQ-9 score less than or equal to 14
Disqualifiers
Inability to perform any of the assessments required for endpoint analysis
Known hypersensitivity to investigational products
Participants with a history of substance abuse, drugs, heavy use of alcohol, and/or smoking within last 5 years
Advanced chronic illness that would impair follow-up or monitoring
Trial design
Treatments tested in this trial
- De-stress & happy gut powder-U001
- De-Stress & Happy Gut powder-I001
- Placebo Powder 001
Treatment groups
81 Participants
are divided into 3 treatment groupsLocations
Sponsors and collaborators
Source ClinicalTrials.gov