Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT05886543 |
Other study ID # |
341989 |
Secondary ID |
|
Status |
Completed |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
September 30, 2021 |
Est. completion date |
January 30, 2023 |
Study information
Verified date |
May 2023 |
Source |
Cairo University |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
Sixty patients with 25-45 years of age presenting post burn inhalation injury, randomly
distributed into two equal groups, 30 patients for each group. control group receive
conventional chest physiotherapy (diaphragmatic respiratory exercises, apical breathing
exercises) for (15-20) minutes 3times/week and medical treatment for 4 weeks as a total
period of treatment. study group will receive pilates exercise in addition to their
conventional chest physiotherapy for (15-20) minutes 3times/week and medical treatment for 4
weeks as a total period of treatment, computerized spirometer assessment before treatment are
( The following variables were measured: forced vital capacity (PVC%) and forced ·expiratory
volume in one second (FEVl %) and peak expiratory flow (PEF %)and after one month
Description:
Two groups of sixty patients (thirty patients in each group) of both sexes of inhalation
injury post burn are selected randomly to participate in the study.
The patients will be divided into two equal groups in number:
- Group (A) study group: this group includes 30 patients who have postburn inhalation
injury will receive conventional chest physiotherapy (diaphragmatic respiratory
exercises, deep inhalation exercises, and respiratory exercises associated with shoulder
flexion movements and extension of the upper limbs, assisted cough, circulatory
exercises and early ambulation) and medical treatment and pilates method.
- Group (B) control group: this group includes 30 patients who have postburn inhalation
injury will receive conventional chest physiotherapy (diaphragmatic respiratory
exercises, deep inhalation exercises, and respiratory exercises associated with shoulder
flexion movements and extension of the upper limbs, assisted cough, circulatory
exercises and early ambulation) and medical treatment.
- computerized spirometer assessment before treatment are ( The following variables were
measured: forced vital capacity (PVC%) and forced ·expiratory volume in one second (FEVl
%) and peak expiratory flow (PEF %)and after one month