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Effect of anulom vilom practice in change of vital parameters

Phase 3
Registration Number
CTRI/2024/05/066710
Lead Sponsor
Dr Ankita Laxman Bhandari
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Subjects from the age group of 18 years to 60 years will be included.

- Subjects will be included irrespective of gender, occupation and religion.

- Subject who can practice Anulom Vilom in a 1:2 ratio.

Exclusion Criteria

-Subjects with any metabolic and psychological disorders will not be the part of study.

-Subject who cannot practice Anulom Vilom will be excluded.

-Subject who cannot practice Anulom Vilom in a ratio 1:2.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Beneficiary changes in vital parameters i.e. pulse rate, O2 saturation level, systolic & diastolic blood pressureTimepoint: After every 4 weeks
Secondary Outcome Measures
NameTimeMethod
Complete effective change in vital parametersTimepoint: 30 days
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