Effects of Chest Expansion Exercises on Thoracic Expansion and VO2 Max in Children With Chest Burn

December 12, 2024 updated by: Riphah International University
Burns are injuries to the skin or tissues caused by heat, electricity, chemicals, friction, or radiation. They can result from flames, hot solids, or liquids. In intensive care, physiotherapy often includes sitting exercises, passive motions, and active training, which are essential for recovery after burns. This study aims to evaluate the impact of chest expansion exercises using a stretch pole on chest expansion and VO2 max in children with chest burns. Conducted as a quasi-experimental study at Jinnah Burn Centre in Lahore, it will involve 33 participants selected through non-probability convenience sampling. Data collection will span six months. Thoracic expansion will be measured with an inch tape, and VO2 max will be calculated using a specific formula. Routine physiotherapy, including range of motion exercises and soft tissue massage, will be administered alongside chest expansion exercises for 20 minutes daily, five days a week, over three weeks.

Study Overview

Status

Active, not recruiting

Conditions

Intervention / Treatment

Detailed Description

Burns are a kind of injury that can occur to the skin or other tissues. Acute trauma can be brought on by heat, electricity, chemicals, friction, radiation, or other factors. Burns are a kind of injury that can occur to the skin or other tissues. Acute trauma can be brought on by heat, electricity, chemicals, friction, radiation, or other factors. Burn are many types of burn Flames (flame burns), hot solids (contact burns), or hot liquids (scalds). Sitting out of bed, passive motions, and active/assisted exercises were frequent physiotherapy therapies in the intensive care unit. After a burn injury, exercise training serves as a significant and useful technique for achieving physical health. The objective of this study is to check the effect of chest expansion exercises by using stretch pole on chest expansion and VO2 max in children with chest burn. This study will be a Quasi-Experimental study .Data will be collected from Jinnah Burn Centre, Lahore. Data will be collected within 6 month from approval date of synopsis. Sample size is 33. Non-probability convenience sampling technique will be used in this study. Thoracic expansion will be measured by inch tape and vo2 max will be calculated by using a formula. Routine physiotherapy will be provided to the subjects routinely with chest expansion exercises. In routine physiotherapy, Range of motion exercises, Soft tissue massage, positioning to prevent the pressure sores will be provided for almost 20 minutes. The chest expansion exercises will be provided to the patients by using stretch pole for 20 minutes. All the interventions will be given to patients for 5 days in a week on daily basis for 3 weeks

Study Type

Interventional

Enrollment (Estimated)

33

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Punjab
      • Lahore, Punjab, Pakistan
        • Riphah International University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Age: 5- 10 years.
  • Children with mild to moderate chest burn.
  • Children with decreased mobility due to chest burn.

Exclusion Criteria:

  • Chest burns with any post-burn complications,
  • Neurological impairments,
  • Contracture due to immobility,
  • Infection due to chest burn.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Quasi Group
A group of 33 children of age 5-10 years with chest burn. The techniques include deep breathing with shoulder abduction, deep breathing and relaxing with hip external rotation with slight knee flexion, floor polishing motion; rounded hands to draw small circles on the floor etc.
Range of motion Exercises, soft tissue massage, positioning to prevent pressure sores, stretch pole for 20 minutes

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Chest Expansion
Time Frame: 6 months
Chest expansion refers to the increase in chest cavity size during breathing, essential for effective lung function and oxygen intake.
6 months
VO2 Max
Time Frame: 6 months
VO2 max is the maximum amount of oxygen the body can utilize during intense exercise, reflecting aerobic fitness and cardiovascular health.
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Kashaf Ahmad, MS*, Riphah International University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 12, 2024

Primary Completion (Actual)

October 10, 2024

Study Completion (Estimated)

December 17, 2024

Study Registration Dates

First Submitted

November 12, 2024

First Submitted That Met QC Criteria

December 12, 2024

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

December 12, 2024

Last Verified

December 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • REC/RCR/AHS/24/Kashaf

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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