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Effect of Yogic Breathing and Relaxation versus Standard Non-Pharmacological Treatment on Blood Pressure.

Efficacy of 12-week practice of Yogic Breathing and Relaxation vs Standard non-pharmacological interventions on Blood Pressure and Lifestyle parameters among Hypertensive adults: A Randomized Control Trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/063355
Enrollment
66
Registered
2024-02-29
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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: Pranayama and Yoga Nidra Meditation: Breathing exercises and Yoga Nidra Meditation shall be taught to participants on their day of enrollment in the study. Participants shall follow thi

Sponsors

AIIMS RISHIKESH
Lead Sponsor
SELF FUNDED
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Participants must be 18 years to 55 years of age. 2. Diagnosed with Elevated BP and Stage 1 Hypertension (classified as per AHA/ACC guidelines). 3. Should agree to do regular yoga practice based on yoga module.

Exclusion criteria

Exclusion criteria: 1. Practicing Yoga/Meditation for more than 1 month in the previous 6 months. 2. Having Comorbidities like Diabetes Mellitus, Chronic Kidney Disease, Established Cardiovascular Disease, Stroke, Epilepsy, Migraine or Psychiatric Disorder. 3. Not willing to provide written informed consent. 4. Pregnant Women. 5. Less than 75% compliance.

Design outcomes

Primary

MeasureTime frame
To determine the efficacy of pranayama and meditation in participants with hypertension and compare them with standard non pharmacological treatment for blood pressure reduction.Timepoint: All outcomes will be assessed at four time points, i.e., at enrollment, i.e., baseline, after four weeks of baseline, after eight weeks of baseline and final assessment will be conducted after twelve weeks of baseline.

Secondary

MeasureTime frame
o Sleep Quality using Pittsburgh Sleep Quality Index (PSQI) o Perceived stress levels (using Perceived Stress Scale) o Physical Activity Levels (using Global Physical Activity Questionnaire) o Alcohol usage (using Alcohol Use Disorder Identification Test) o Socioeconomic status (using updated KuppuSwamy Socioeconomic Scale) o Anthropometric Measurements: height (cm), weight (kg), body mass index (kg/m2), hip circumference (cm), waist circumference (cm) and waist to hip ratio. Timepoint: All outcomes will be assessed at four time points, i.e., at enrollment, i.e., baseline, after four weeks of baseline, after eight weeks of baseline and final assessment will be conducted after twelve weeks of baseline.

Countries

India

Contacts

Public ContactRajat Sharma

AIIMS, Rishikesh

anshupathania27@gmail.com8126021556

Outcome results

None listed

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