None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Inclusion Criteria: 1)Male and Female participants, between the age group of 18 years to 60 yrs. 2)Participants who are willing to give written, signed and dated informed consent to participate in the study.
Exclusion criteria
Exclusion criteria: 1.Participants below the age of 18yrs 2. Any condition that is considered unfit for study may interfere with the study 3.Participants with a history of chronic respiratory Distress, CVS problems, red blood disorders. 4.Participants on regular medication
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Association of Prakriti with the bala, Respiratory parameters like respiratory rate, spirometery parameters- EVC, EPV. Complete Haemogram will be obtained. The outcome of this study is scientific and practical scrutiny of ancient thought of bala. This study will further show the bala across various prakriti Timepoint: 1. CTRI approval and study initiation -15days (baseline) 2. Data collection- 3months from study initiation with Prakriti assessment Will be done using CCRAS Prakriti assessment scale. 1-3months(after approval) 2.Respiratory parameters using spirometer, CVS, Bala examination with questionnaire , Blood will be taken from volunteers for haemogram.(1-3 months after approval) Data cleaning and analysis and reporting -1month(after completing data collection). | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. To study the association of respiratory parameters across deha prakriti. 2.To study the association haemogram, cardiovascular parameters across Deha Prakriti types.Timepoint: 1.To study prevalance of any disorders in the subjects of different deha prakriti types (4th month- during data analysis) | — |
Countries
India
Contacts
KAHER Shri B.M.K Ayurveda Mahavidyalaya