NCT07320742

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
74

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Aug 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 21, 2025

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

December 8, 2025

Completed
28 days until next milestone

Study Completion

Last participant's last visit for all outcomes

January 5, 2026

Completed
1 day until next milestone

First Posted

Study publicly available on registry

January 6, 2026

Completed
Last Updated

April 24, 2026

Status Verified

August 1, 2025

Enrollment Period

2 months

First QC Date

December 8, 2025

Last Update Submit

April 23, 2026

Conditions

Keywords

pranayamapulmonary function testbreathing exerciseoxygen saturationStress, Psychologicalpostural balance

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

EXPERIMENTAL
Behavioral: Slow Pranayama

Fast Pranayama Group

EXPERIMENTAL
Behavioral: Fast Pranayama

Interventions

Slow PranayamaBEHAVIORAL

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.

Slow Pranayama Group
Fast PranayamaBEHAVIORAL

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.

Fast Pranayama Group

Eligibility Criteria

Age18 Years - 35 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

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)

Location

MeSH Terms

Conditions

Stress, Psychological

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehavior

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

Locations