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Assessment of effect of nadhi shodhan pranayam in hypertension.

An exploratory randomised trial to assess the effect of nadhi shodhan pranayam as adjunct versus standard non pharmacological management in subjects with hypertension. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/11/059625
Enrollment
64
Registered
2023-11-07
Start date
Unknown
Completion date
Unknown
Last updated
2023-11-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: I10- Essential (primary) hypertension

Interventions

Intervention1: Nadishodhan pranayam in addition to standard pharmacological treatment.: 10 min of nadishodhan pranayam on first visit and daily for 10 min for 6 weeks. Control Intervention1: Standard

Sponsors

Non funded
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Newly diagnosed & self-reported cases of Hypertension on medication. 2) Able to follow verbal instructions. 3) Having adequate understanding of English or Hindi. 4) Able to sit without physical discomfort for 10 minutes. 5) Those having smart phone/smart devices and internet access

Exclusion criteria

Exclusion criteria: 1) Inability to independently provide informed consent. 2) Patients presenting with Hypertensive Emergency. 3) Already practicing any kind of pranayam. 4) Patients who at follow-up practice nadhi shodham pranayam for < 63 days.

Design outcomes

Primary

MeasureTime frame
To assess the effect of nadhi shodhan pranayama on blood pressureTimepoint: At first visit, immediately after intervention and follow up after 6 weeks.

Secondary

MeasureTime frame
1) To assess the effect of nadhi shodhan pranayama on heart rate variability (HRV). 2) To assess the effect of nadhi shodhan pranayama on sleep & anxiety.Timepoint: At first visit and follow up after 6 weeks.

Countries

India

Contacts

Public ContactMonika Pathania

AIIMS Rishikesh

Anshupathania27@gmail.com8126021556

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026