Pranayama Effect on Autonomic Nervous System Clinical Trial
— PYAMAOfficial title:
The Effect of Respiration Rate During Pranayama Practice on the Autonomic Nervous System
Verified date | March 2023 |
Source | National University of Natural Medicine |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The proposed study design will be a randomized, cross-over trial testing different pranayama breathing interventions. Participants (N=40) will perform each of the following five interventions in a randomly assigned order: (1) internal-paced pranayama intervention (Sheetali/Sheetkari for 10 minutes each) (2) internal-paced deep breathing control (3) external-paced pranayama intervention at a rate of 6 bpm (4) external-paced deep breathing at a rate of 6 bpm (5) sitting quietly with no external instruction.
Status | Completed |
Enrollment | 25 |
Est. completion date | July 21, 2021 |
Est. primary completion date | May 15, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 25 Years to 55 Years |
Eligibility | Inclusion Criteria: - Able to roll tongue into tube (queried over the phone and reassessed at visit 1) - Age = 25 and = 55 (HRV and other ANS parameters change significantly during the aging process) - BMI = 18.5 and = 34.9 (Body weight effects HRV and ANS parameters) - Willing and able to give informed consent - Able to follow protocol and attend visits - Able to read and write English - Able to abstain from over-the-counter painkillers like NSAIDs and allergy medications for 24 hours (Zyrtec and Claritin) Exclusion Criteria: - A regular practice of yoga, meditation, and/or breathing more than once a week (Individuals that have conditioned their ANS through yoga, meditation, and breathing exercise may not respond to the breathing condition like the representative population) - Formal (Yoga Alliance Sanctioned 200h or 500h course or other comparable ) training in yoga, Mindfulness-Based Stress Reduction, transcendental meditation, Qigong, Tai Chi, and/or other forms of meditation/consciousness expansion practices (Individuals that have conditioned their ANS through yoga, meditation, and breathing exercise may not respond to the breathing condition like the representative population) - A recent cardiovascular event (e.g. myocardial infarction, stroke = six months prior to screening visit), current coronary artery disease, angina, stage III or IV congestive heart failure, or stated history of coronary bypass surgery or heart stent placement - Presence of a cardiac pacemaker - History of cardiovascular disease, including heart arrhythmias and prehypertension (systolic BP > 140 mmHg or diastolic BP >90) or hypotension (systolic BP < 90 mmHg or diastolic BP <60) - Taking prescription drugs that may interfere with heart, nervous, and respiratory rhythms, beta blockers, pain medications, SSRIs, anti-cholinergics, or anxiety medication - Started or changed the dosage of supplements or medications within the last month - Open skin rashes and sores that may interfere with placement of sensors - History of emphysema, chronic bronchitis or bronchiectasis and/or asthma (with FEV1/FVC < 80%) within in the last six months or taking medication to control asthma symptoms - History of Diabetes type 1 or 2 (> 5 year duration of type 2 diabetes or > 10 years duration of type 1 diabetes (due to the potential for autonomic neuropathy) - History of or current epilepsy or other seizure disorder(s) - Current diagnosis of mental illness for which the participant is currently taking prescription medications - Smoking of tobacco products in a the last 6 months - Pregnant, nursing, or planning a pregnancy within the next 6 weeks (due to pregnancy-induced changes in HRV - Presence of any unstable and/or significant medical disorder that would compromise the participant's safety to take part in the trial. Such disorders include any known event that will require beginning new medications and/or prevent adherence to the schedule of study activities over the following 6 weeks - Chronic hyperventilation (Access by NQ during telephone screen) |
Country | Name | City | State |
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United States | National University of Natural Medicine | Portland | Oregon |
Lead Sponsor | Collaborator |
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National University of Natural Medicine |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Change in PANAS Questionnaire | Mood Evaluation | Before and after 20 minutes of breathing excersise | |
Other | Change Mindfullness Questionnaire | Evaluation of body awareness | Before and after 20 minutes of breathing excersise | |
Primary | Change in Heart Rate Variability (HRV) | Analysis of EKG spectra before and after the session | Before and after 20 minutes of breathing excersise | |
Secondary | Change in EEG | Analysis of EEG spectra before and after the session | Before and after 20 minutes of breathing excersise |