Fast vs. Slow Pranayama for Breathing, Heart, Balance, and Well-Being in Students
Comparison of the Effects of Fast and Slow Pranayama Techniques on Respiratory, Cardiovascular, Balance, and Psychosocial Parameters in University Students
1 other identifier
interventional
74
1 country
1
Brief Summary
The goal of this clinical trial is to compare the effects of slow and rapid pranayama techniques on respiratory, cardiovascular, balance, and psychosocial parameters in healthy adults aged 18-35 years. The main questions it aims to answer are: Do slow and rapid pranayama techniques produce different improvements in lung volumes and peak cough flow? Does slow pranayama lead to greater improvements in oxygen saturation and cardiovascular parameters, while rapid pranayama provides greater gains in balance and respiratory flow values? Researchers will compare a slow pranayama group (n = 39) and a rapid pranayama group (n = 39) to determine how breathing speed influences physiological and psychosocial outcomes. Participants will: Be randomly assigned to one of two groups (slow or rapid pranayama). Practice their assigned pranayama techniques for 25-30 minutes, 4 days per week for 12 weeks (one supervised, three home-based sessions). Undergo pre- and post-intervention assessments including spirometry (FVC, FEV₁, FEF25%-75%, PEF), oxygen saturation, peak cough flow, blood pressure, heart rate, balance tests (single-leg stance, Y-Balance Test), and validated questionnaires for perceived stress, anxiety, depression, fatigue, and sleep quality. This study aims to clarify how controlled breathing speed influences respiratory efficiency, cardiovascular regulation, postural stability, and mental well-being in young adults, contributing to evidence-based recommendations for integrating pranayama into stress-management and preventive rehabilitation programs.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Aug 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 16, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 21, 2025
CompletedFirst Submitted
Initial submission to the registry
December 8, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
January 5, 2026
CompletedFirst Posted
Study publicly available on registry
January 6, 2026
CompletedApril 24, 2026
August 1, 2025
2 months
December 8, 2025
April 23, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Forced Expiratory Flow at 25-75% of FVC (FEF25-75)
FEF25-75 is the average flow rate during the middle half of the FVC maneuver. It is often considered a sensitive indicator of small airway function. Measurements will be carried out using the COSMED PONY FX (Italy) device, ensuring compliance with ATS/ERS standards. The values will be recorded in liters per second (L/s).
From enrollment to the end of treatment at 12 weeks
Secondary Outcomes (14)
Forced Vital Capacity (FVC)
From enrollment to the end of treatment at 12 weeks
Forced Expiratory Volume in 1 Second (FEV1)
From enrollment to the end of treatment at 12 weeks
FEV1/FVC Ratio
From enrollment to the end of treatment at 12 weeks
Peak Expiratory Flow (PEF)
From enrollment to the end of treatment at 12 weeks
Peak Cough Flow (PCF)
From enrollment to the end of treatment at 12 weeks.
- +9 more secondary outcomes
Study Arms (2)
Slow Pranayama Group
EXPERIMENTALFast Pranayama Group
EXPERIMENTALInterventions
Participants will practice pranayama in a quiet room, comfortably seated (sukhasana), maintained at a comfortable temperature (24 ± 2°C). Sessions typically take place as follows: Participants in the Slow Pranayama Group will practice the Anuloma Viloma, Savitri, and Ujjayi breathing techniques. Slow pranayama breathing will be practiced for two minutes, with one-minute rests between each breathing technique, for a total of three cycles. Each cycle will last approximately nine minutes. Participants in both groups will rest in savasana for 10 minutes at the end of the session. No drugs or devices are used. The intervention is a controlled breathing exercise technique.
Participants will practice pranayama in a quiet room, comfortably seated (sukhasana), maintained at a comfortable temperature (24 ± 2°C). Sessions will typically be conducted as follows: Participants in the Fast Pranayama Group will practice Kapalabhati, Bhastrika, and Agnisar breathing. Each breathing technique will be practiced for one minute, followed by a one-minute rest. This will be practiced for a total of four cycles. Each cycle will last approximately six minutes. No drugs or devices are used. The intervention is a controlled breathing exercise technique.
Eligibility Criteria
You may qualify if:
- Between age 18-35
You may not qualify if:
- Subjects who have practiced yoga techniques in the last year.
- Subjects with a history of previous or current organic disease.
- Subjects who cannot practice pranayama due to physical abnormalities.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Istanbul Medipol University
Istanbul, Istanbul, 34810, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
December 8, 2025
First Posted
January 6, 2026
Study Start
August 16, 2025
Primary Completion
October 21, 2025
Study Completion
January 5, 2026
Last Updated
April 24, 2026
Record last verified: 2025-08