Actively Recruiting

Phase Not Applicable
Age: 40Years - 55Years
All Genders
NCT06537479

Combined Effects of Buteyko Breathing Technique and Chest Wall Mobilization on Pulmonary Functions and Quality of Life

Led by Riphah International University · Updated on 2024-08-05

40

Participants Needed

1

Research Sites

12 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The study aims to evaluate the effects of Buteyko breathing techniques with and without chest wall mobilization on pulmonary functions, and quality of life in chronic smokers. The study design will be a randomized clinical trial. The study will be completed in 10 months after the approval of the synopsis from the Ethical Committee of RCRS \& AHS. A non-probability convenient sampling technique will be used to recruit the individuals. Group 1-Buteyko breathing technique + Chest Wall Mobilization and Group 2-Buteyko Breathing Technique + Without Chest Wall Mobilization

CONDITIONS

Official Title

Combined Effects of Buteyko Breathing Technique and Chest Wall Mobilization on Pulmonary Functions and Quality of Life

Who Can Participate

Age: 40Years - 55Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Both male and female participants were included
  • Age between 40 and 55 years
  • Must be current smokers or have a history of long-term smoking
  • Must meet smoking criteria calculated by number of packs per day multiplied by years smoked
  • Predicted lung function values with FEV1 less than 75% and FEV1/FVC ratio less than 70%
Not Eligible

You will not qualify if you...

  • Neurological disorders
  • Musculoskeletal disorders affecting physical activity
  • Any pulmonary complications or lung diseases
  • Previous involvement in any other exercise or physical activity

AI-Screening

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Trial Site Locations

Total: 1 location

1

University of Lahore Teaching Hospital

Lahore, Punjab Province, Pakistan, 54000

Actively Recruiting

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Research Team

K

Kinza Saleem, DPT

CONTACT

T

Tasneem Shahzadi, TDPT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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