None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Apparently Healthy Males / Female Volunteers aged between 25 to 50 years. 2. Volunteers willing to sign the consent form for clinical trial and agreeing to participate sincerely.
Exclusion criteria
Exclusion criteria: 1. Volunteers with history of chronic disease like severe Hypertension, IHD, COPD, DM, Cancer, Hepatic & Renal insufficiency, psychotic disorder like depression, schizophrenia. 2. History of any acute/ serious illness. 3. Pregnant / lactating woman. 4. History of HIV. 5. Volunteers who have completed participation in any other clinical trial during the past six (06) months. 6. Any other condition which the Investigator thinks may jeopardize the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Scoring pattern for Balya from PhD thesis of Dr Paparinath, 2007 under the guidance of Prof. R.R.Dwivedi, HOD Dept of Basic Principles, IGPTRA, Jamnagar. 2. Anthropometric measurements. 3. Muscular Strength and endurance assessmentTimepoint: 3 months (90 Days) | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Scoring pattern for Balya from PhD thesis of Dr Paparinath, 2007 under the guidance of Prof. R.R.Dwivedi, HOD Dept of Basic Principles, IGPTRA, Jamnagar. 2. Anthropometric measurements. 3. Muscular Strength and endurance assessment 4. Biochemical investigations 5. Hematological investigationsTimepoint: 1. 1 month (30 Days), 2 month (60 Days) 2. 1 month (30 Days), 2 month (60 Days) 3. 1 month (30 Days), 2 month (60 Days) 4. 3 months (90 Days) 5. 3 months (90 Days) | — |
Countries
India
Contacts
National Institute of Ayurveda