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Effect of yoga breathing techniques on brain activity

Completed
Conditions
Participants with normal health of both gender (based on Semi structured interview for health conditions)
Registration Number
CTRI/2021/11/037922
Lead Sponsor
Patanjali Research Foundation Trust
Brief Summary

The aim of this study is to assess the effects of (i) Yoga bellows-type breathing (*bhastrika pranayama*), (ii) High frequency yoga breathing (*kapalabhati pranayama*) and (iii) Humming bee breathing (*bhramari pranayama*) techniques on thalamo-cortical and autonomic activity in normal healthy participants. Assessments used in this study are: (i) Middle latency auditory evoked response (MLR) for thalamo-cortical activity using Nicolet EDX system U.S.A., (ii) Heart rate variability (HRV) and respiration rate (RR) for involvement of autonomic nervous system using MP 45 Biopac Student Lab, BIOPAC System Inc, U.S.A, (iii) The brief mood introspection scale (BMIS) for mood, (iv) Nijmegen questionnaire (NQ) for breathing pattern and (v) Visual analogue scale (VAS) for interventional quality. This study will help to understand if the characteristics of respiration modify the thalamo-cortical activity as well as involvement of autonomic nervous system to modify this.

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
40
Inclusion Criteria
  • Healthy adults (health status is based on a semi-structured interview) 2.
  • Minimum yoga experience 3 months.
Exclusion Criteria
  • Person having any health conditions which could make it unsafe to practice of any pranayama.
  • The health conditions unsafe to practice high frequency yoga breathing and yoga bellows-type breathing are epilepsy, hypertension, history of stroke, gastric ulcer, hernia, glaucoma, recent abdominal surgery and pregnancy.
  • Tinnitus and an active ear infection are the conditions which are unsafe to practice humming bee breathing.
  • Person with extra systole based on electrocardiogram (ECG) 3.
  • Person with abnormal evoked response based on mid-latency auditory response (MLR) 4.
  • Having any type of skin allergy 5.
  • Consumption of alcohol, tobacco, caffeine and also intake of medication (before and during the days of recording).

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Middle latency auditory evoked response (MLR),In each session there will be (i) Baseline (5 minutes), (ii) During (18 minutes with three epochs of 5 minutes with one minute rest between two consecutive epochs) and (iii) Post (5 minutes).
2. Heart rate variability (HRV) andIn each session there will be (i) Baseline (5 minutes), (ii) During (18 minutes with three epochs of 5 minutes with one minute rest between two consecutive epochs) and (iii) Post (5 minutes).
3. Respiration rate (RR).In each session there will be (i) Baseline (5 minutes), (ii) During (18 minutes with three epochs of 5 minutes with one minute rest between two consecutive epochs) and (iii) Post (5 minutes).
Secondary Outcome Measures
NameTimeMethod
1. Mood using Brief mood introspection scale (BMIS),2. Symptoms of hyperventilation syndrome using Nijmegen questionnaire (NQ) and

Trial Locations

Locations (1)

Patanjali Research Foundation (Trust)

🇮🇳

Hardwar, UTTARANCHAL, India

Patanjali Research Foundation (Trust)
🇮🇳Hardwar, UTTARANCHAL, India
Dr Shirley Telles
Principal investigator
9897963254
office@prft.in

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