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Pilates Exercise and Inhalation Injury Post Burn (burn)

K

Khadra Mohamed Ali

Status

Completed

Conditions

Inhalation Injury

Treatments

Behavioral: Conventional chest physical therapy
Behavioral: Pilates exercise

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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

Full 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

Enrollment

60 patients

Sex

All

Ages

25 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ranged between 25-45 years.
  • All patients presented post-burn inhalation injury.
  • Patients with facial burn or upper limb burn.
  • All patients would be free of acute or chronic pulmonary disease and will have the capacity to perform the protocol evaluation tests properly.
  • All patients enrolled to the study would have their informed consent.

Exclusion criteria

  • Cardiac diseases.
  • Chronic pulmonary disorders.
  • Previous or present smoking history.
  • Female patients who are pregnant and lactating.
  • Post-burn patient on ICU.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

control group
Experimental group
Description:
this group includes 30 patients who have post burn inhalation injury will receive 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
Treatment:
Behavioral: Conventional chest physical therapy
Behavioral: Pilates exercise
study group
Experimental group
Description:
this group includes 30 patients who have post burn inhalation injury 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.omputerized 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
Treatment:
Behavioral: Conventional chest physical therapy
Behavioral: Pilates exercise

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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