None listed
Conditions
Interventions
None listed
Sponsors
Pratiksha trust
Eligibility
Inclusion criteria
Inclusion criteria: 1. Participants of both the genders aged 25 to 85 years 2. Literate population (minimum 10th pass) 3. Individuals should be able to perform daily living activities independently. 4. Willing to sign the informed consent letter and participate in the study.
Exclusion criteria
Exclusion criteria: 1. Dementia (CDR less than 1 & MoCA more than 23 scores) 2. Severe hearing or visual impairment which can alter cognitive test outcome 3. Patients with uncontrolled diabetes (HbA1C less than 7.0) 4. Patients with uncontrolled hypertension according to physicians assessments. 5. Hyper-lipidaemia (Fredrickson s classification) 6. Hypothyroid patients on medications 7. Major psychological or psychiatric illness and on any anti-depressants, anti-psychotic drug etc. for long term (more than 6 months). 8. Head trauma in the past. 9. Alcohol & drug addicts. 10. Severe metabolic disorder of any kind as reflected in clinical history or clinical questionnaire.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Improvement in cognitive function (attention, learning and memory, spatial memory, and visuospatial tasks) and related parameters (structural and functional MRI) in BG group compared to Plain Ghee (PG), BE and Placebo group.Timepoint: 12/24/36 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Correlation of cognitive performance and effect of formulations with blood profile, Prakriti and other related parameters (stress, anxiety sleep, depression, irritability and quality of life)Timepoint: 12/24/36 weeks | — |
Countries
India
Contacts
Public ContactDr Ashwini Godbole
The University of Trans-Disciplinary Health Sciences and Technology (TDU)
Outcome results
None listed