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How device assisted regulation of normal breath changes the autonomic functions in patients with non-communicable lifestyle conditions

Voluntary regulated breathing for non-communicable diseases

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/11/038289
Enrollment
300
Registered
2021-11-26
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Health Condition 1: E119- Type 2 diabetes mellitus without complications Health Condition 2: I10- Essential (primary) hypertension Health Condition 3: E663- Overweight

Interventions

Intervention1: Device guided normal breathing: Intervention arms: There will be two interventional sessions including device guided normal breathing with (i)exhale ratio greater than inhale ratio (ii)

Sponsors

Patanjali Research Foundation Trust
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients will be screened and recruited based on (i) Diagnosis as per ICMR guidelines and case history obtained by a clinician for lifestyle conditions i.e., diabetes, hypertension, and obesity (ii) Semi-structured interviews

Exclusion criteria

Exclusion criteria: (i) Patients with an extra systole based on EKG recordings (ii) Patients with conditions i.e., cardiovascular disease, respiratory disorders, malignancy, chronic pain and arthritis

Design outcomes

Primary

MeasureTime frame
Autonomic functions (i) Heart rate variability (ii) Respiration rateTimepoint: (i) Before the intervention (ii) During the intervention (iii) After the intervention

Secondary

MeasureTime frame
Physiological outcomes (i) Systolic blood pressure (ii) Diastolic blood pressure (iii) Mean arterial pressure (iv) Oxygen saturationTimepoint: (i) Before the intervention (ii) During the intervention (iii) After the intervention;Psychological outcomes feelings of anxiety, calmness, discomfort and relaxation through visual analog scale Timepoint: (i) Before the intervention (ii) After the intervention

Countries

India

Contacts

Public ContactDr Shirley Telles

Patanjali Research Foundation (Trust)

office@prft.in9897963254

Outcome results

None listed

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