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Clinical Trials/NCT05603507
NCT05603507
Completed
Not Applicable

Inspiratory Muscle Training Effects on Pulmonary Function and Quality of Life in Children With Chest Burn

Qassim University1 site in 1 country40 target enrollmentSeptember 10, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Burns
Sponsor
Qassim University
Enrollment
40
Locations
1
Primary Endpoint
Pulmonary function test, FEV1/FVC ratio
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

8 weeks of inspiratory muscle training combined with a pulmonary rehabilitation program increases respiratory muscle strength, pulmonary function, functional capacity, and quality of life in chest burned children.

Detailed Description

The primary purpose of this study is to see how an inspiratory muscle training program along with a pulmonary rehabilitation program improved respiratory muscle strength, respiratory function and quality of life after children with chest burns were discharged from the hospital.

Registry
clinicaltrials.gov
Start Date
September 10, 2021
End Date
May 15, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Maged Basha

Assistant Professor, College of Medical Rehabilitation, Qassim University

Qassim University

Eligibility Criteria

Inclusion Criteria

  • Children aged 10 to
  • Following hospital discharge.- Total body surface area (TBSA) of 30% to 50%.
  • Chest burns.
  • Deep partial to full thickness burns.
  • Subjects who had a skin graft or who healed completely were also included.

Exclusion Criteria

  • - Participants who had a nonhealing or open wound.
  • Congenital diaphragmatic hernia.
  • Chest wall deformity.
  • Cardiac or pulmonary problems.

Outcomes

Primary Outcomes

Pulmonary function test, FEV1/FVC ratio

Time Frame: 8 weeks

performed using a spirometer, (forced expiratory volume in the first second/ forced vital capacity) FEV1/FVC ratio was recorded.

maximal inspiratory pressure

Time Frame: 8 weeks

performed using an electronic respiratory pressure meter

maximal expiratory pressure

Time Frame: 8 weeks

performed using an electronic respiratory pressure meter

Pulmonary function test, forced expiratory volume in the first second

Time Frame: 8 weeks

performed using a spirometer, the FEV1 (forced expiratory volume in the first second) was recorded.

Pulmonary function test, forced vital capacity

Time Frame: 8 weeks

performed using a spirometer, the FVC (forced vital capacity) was recorded.

Secondary Outcomes

  • Functional exercise capacity(8 weeks)
  • Health related Quality of Life(8 weeks)

Study Sites (1)

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