NCT07140458

Brief Summary

The aim of this study was to evaluate the Effectiveness of Box Breathing Technique and Buteyko breathing techniques in patients with Asthma, using both Clinical Pulmonary tests as well as Patient reported outcomes.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
36

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Dec 2024

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 17, 2024

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 14, 2025

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 2, 2025

Completed
12 days until next milestone

First Submitted

Initial submission to the registry

July 14, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

August 24, 2025

Completed
Last Updated

August 24, 2025

Status Verified

August 1, 2025

Enrollment Period

2 months

First QC Date

July 14, 2025

Last Update Submit

August 18, 2025

Conditions

Keywords

AsthmaBreathing ExerciseButeyko BreathingBox BreathingPulmonary Function tests

Outcome Measures

Primary Outcomes (3)

  • Lung Function tests (FVC)

    Changes from Baseline, Lung function tests measure how well the lungs take in, hold, and move air, as well as how efficiently they transfer oxygen into the blood. These tests help diagnose and monitor respiratory diseases like asthma, COPD, pulmonary fibrosis, and restrictive lung diseases. Tets measures are compared against Normal value i.e: FVC ≥80%.

    through study completion, approximately 8 weeks

  • Lung Function Test (FEV¹)

    Changes from Baseline, Lung function tests measure how well the lungs take in, hold, and move air, as well as how efficiently they transfer oxygen into the blood. These tests help diagnose and monitor respiratory diseases like asthma, COPD, pulmonary fibrosis, and restrictive lung diseases. Test measures are compared against Normal value i.e: FEV¹ ≥80%.

    through study completion, approximately 8 weeks

  • Lung Function test (FEV₁/FVC ratio)

    Changes from Baseline, Lung function tests measure how well the lungs take in, hold, and move air, as well as how efficiently they transfer oxygen into the blood. These tests help diagnose and monitor respiratory diseases like asthma, COPD, pulmonary fibrosis, and restrictive lung diseases. Test measures are compared against Normal value i.e: FEV₁/FVC ≥0.7.

    through study completion, approximately 8 weeks

Secondary Outcomes (2)

  • Modified Borg Dyspnea Scale

    through study completion, approximately 8 weeks

  • Mcgill quality of life questionnaire

    through study completion, approximately 8 weeks

Study Arms (2)

Buteyko Breathing

EXPERIMENTAL

Using Buteyko Breathing as primary intervention in addition to standard Asthma therapy.

Other: Buteyko Breathing

Box Breathing Technique

EXPERIMENTAL

Using Buteyko Breathing as primary intervention in addition to standard Asthma therapy.

Other: Box breathing

Interventions

Buteyko Breathing is a technique focusing on controlled, reduced breathing to improve oxygen uptake and reduce hyperventilation-related symptoms using Air hunger. Procedure:- After gaining proper relaxation: 1. Exhale slowly, and then hold that breath. 2. Use the index finger and thumb to plug the nose. 3. Hold that breath until there is an urge to breathe, and then inhale. 4. Breathe normally for at least 10 seconds. 5. Repeat several times.

Buteyko Breathing

Box Breathing (4-4-4-4 Technique) - Box Breathing exercises boosts lung function by optimizing oxygen flow and activating relaxation responses.Each exercise Sessions included 20 cycles of Box Breathing. The procedure of the box breathing cycle includes: 1. inhale for 4 seconds 2. Hold the breath for 4 seconds 3. Exhale for 4 seconds 4. Hold the breath for 4 seconds, and repeat.

Box Breathing Technique

Eligibility Criteria

Age25 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Subjects with bronchial asthma for more than one year
  • Subjects who are on regular treatment (both inhalers and medication).
  • Subjects who are conscious and cooperative.

You may not qualify if:

  • Subject with recent abdominal, thoracic surgery.
  • Subject with any Disability; Physical or Mental.
  • Subjects who have other chronic respiratory diseases, new or current smoker, and had respiratory tract infection.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Islam center and Teaching Hospital

Sialkot, Punjab Province, 51310, Pakistan

Location

Related Publications (41)

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    BACKGROUND
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    BACKGROUND
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    PMID: 40487067BACKGROUND
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    BACKGROUND
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    BACKGROUND
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    BACKGROUND
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    BACKGROUND
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    BACKGROUND
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    BACKGROUND
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    BACKGROUND
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    BACKGROUND
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    BACKGROUND
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    PMID: 29247426BACKGROUND
  • AbdElmawla Elsaid RA, Zahran WE-k, Elsaid Hafez DM. Comparison of the Effects of Buteyko and Diaphragmatic Breathing Technique on Improving Pulmonary Functions and Asthma Control among Patients with Bro. Egyptian Journal of Nursing and Health Sciences. 2023;4(3):57-75.

    BACKGROUND
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    BACKGROUND
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    BACKGROUND
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    PMID: 22336677BACKGROUND
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    PMID: 10839848BACKGROUND
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    PMID: 36117601BACKGROUND
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    PMID: 17994405BACKGROUND
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    PMID: 24199257BACKGROUND
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    PMID: 33280709BACKGROUND
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    BACKGROUND
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    BACKGROUND
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    BACKGROUND
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    BACKGROUND
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Related Links

MeSH Terms

Conditions

AsthmaDisease

Condition Hierarchy (Ancestors)

Bronchial DiseasesRespiratory Tract DiseasesLung Diseases, ObstructiveLung DiseasesRespiratory HypersensitivityHypersensitivity, ImmediateHypersensitivityImmune System DiseasesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Qurat ul Ain, Masters

    Riphah International University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 14, 2025

First Posted

August 24, 2025

Study Start

December 17, 2024

Primary Completion

February 14, 2025

Study Completion

July 2, 2025

Last Updated

August 24, 2025

Record last verified: 2025-08

Data Sharing

IPD Sharing
Will not share

Locations