None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Screening assessments for apparently healthy individuals will be done on the basis of medical history, Clinical examination, safety laboratory tests (CBC, ESR, LFT, RFT, HbA1c, Lipid profile, Thyroid Profile, complete urine analysis, urine for pregnancy test, HIV & VDRL, ECG, Chest X-ray (PA view). 2. Subjects willing to give voluntarily written informed consent.
Exclusion criteria
Exclusion criteria: • Subjects who are on regular medication for any physical or mental illness. • Subjects who are not willing to participate in the study for 2 years. • Pregnant woman/who are planning for conception/lactating mother. • Subjects with systolic blood pressure above 139 mmHg or diastolic blood pressure above 89 mmHg (as per JNC 7 classification) • Subjects with HbA1c > 6.4 • Subjects withTSH > 10.0 mIU/L • Subjects with Hb level
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| ï?¶Change in Physical and Psychological parameters in terms of SF-36HRQOL questionnairesTimepoint: 1 st day, every month | — |
Secondary
| Measure | Time frame |
|---|---|
| Change in Oral Health Assessment Tool (OHAT) , Change in Hair Whitening Scale (HWS) , Change in Perceived Stress Scale (PSS),Change in Pittsburgh Sleep Quality Index (PSQI) , Change in Wrinkle Severity Rating Scale (WSRS)Timepoint: 1 month, 6 month , 12 month, 24 month | — |
Countries
India
Contacts
Regional Ayurveda Research Institute Vijayawada AP