Clinical Research Directory

Inclusion Criteria: 1. Male and female participants aged 18-50 years both inclusive 2. Suffering from self-reported mild to moderate stress on the PSS scale score less than or equal to 26 3. Scoring 18-26 on the Montreal Cognitive Assessment MoCA 4. No or minimal impairment in activities of daily living: scoring less than 9 on the Functional Activities Questionnaire FAQ 5. Participants willing to participate in clinical trials and who have read understood and signed the informed consent form 6. No severe anxiety and depression on GAD and PHQ-9 scales 7. Able to complete the cognitive assessment tests Exclusion Criteria: 1. Inability to perform any of the assessments required for endpoint analysis 2. Shows signs of Dementia, such as caused by Alzheimer's Disease, acquired immunodeficiency syndrome AIDS, Creutzfeldt-Jakob disease, Lewy Bodies dementia LBD, Cerebrovascular dementia CVD, Progressive Supranuclear Palsy PSP, multiple cerebral infarctions, or normal pressure hydrocephalus NPH, cardiac disease or endocrine disease 3. Have any other neurodegenerative diseases 4. History of a seizure disorder 5. Known hypersensitivity to investigational products 6. Participants with a history of malignancy diagnosed within the past 5 years or currently diagnosed with malignancy 7. Sitting or resting systolic blood pressure of more than 180 mm Hg or diastolic blood pressure of more than 110 mm Hg at Screening. 8. Participants with a history of substance abuse, drugs, heavy use of alcohol, and/or smoking within the last 5 years 9. Participants currently using medications and or supplements that could have cognitive or mood effects including but not limited to nutraceutical, allopathic, ayurvedic herbal extract or supplement 10. Pregnant or lactating women, as well as women of childbearing potential who are not using contraception or intending to conceive during the study 11. Serious illness or any other condition that, in the opinion of the investigator may compromise the safety or compliance of the patient or preclude the successful completion of the study