Actively Recruiting

Phase Not Applicable
Age: 6Years - 12Years
FEMALE
NCT07576478

Effects of Blowing Balloon Therapy FUNCTION, DYSPNEA AND QUALITY OF LIFE IN OBESE CHILDREN

Led by Riphah International University · Updated on 2026-05-08

38

Participants Needed

1

Research Sites

17 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The respiratory system is divided into upper and lower tracts and functions through gaseous exchange, ventilation, and perfusion, with normal breathing depending on lung compliance, airway resistance, and muscular strength. Pulmonary function is assessed using spirometry, particularly Forced Vital Capacity (FVC) and Forced Expiratory Volume in 1 second (FEV₁), which are often reduced in obese children due to excess adipose tissue restricting chest wall expansion and diaphragmatic movement, contributing to dyspnea. This randomized controlled trial will be conducted over 10 months in Lahore at selected hospitals and schools, involving 38 obese children (BMI ≥30), aged 6-12 years with mild to moderate dyspnea (RPE 8-14), who will be randomly assigned to either an experimental group receiving blowing balloon therapy or a control group performing splint running (n=19 each). Participants will be screened using the Borg RPE Scale, and data will be analyzed using SPSS version 20.

CONDITIONS

Official Title

Effects of Blowing Balloon Therapy FUNCTION, DYSPNEA AND QUALITY OF LIFE IN OBESE CHILDREN

Who Can Participate

Age: 6Years - 12Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Obese children with a body mass index (BMI) of 30 or greater
  • Age between 6 and 12 years
  • Children with mild to moderate breathing difficulty (rated 8-14 on the Borg Rating of Perceived Exertion scale)
Not Eligible

You will not qualify if you...

  • Recent asthma attack or respiratory infection within the past 4 weeks
  • Presence of other chronic respiratory diseases such as cystic fibrosis
  • Presence of chronic heart diseases
  • Musculoskeletal, neurological, or other conditions that prevent exercise
  • Unable to walk or perform the exercise program

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Paraplegic Center

Peshawar, Khyber Pakhtunkhwa, Pakistan, 25000

Actively Recruiting

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Research Team

I

imran amjad, phd

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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