The Effect of Chest Physiotherapy Methods Applied Before Aspiration on Respiratory Characteristics
NCT ID: NCT06277817
Last Updated: 2024-02-26
Study Results
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Basic Information
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COMPLETED
NA
78 participants
INTERVENTIONAL
2021-05-19
2022-10-24
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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expiratory rib cage compression group
Expiratory rib cage compression procedure phase; Three hours after the first aspiration data were obtained, before the second aspiration, expiratory rib cage compression was applied for 5 minutes in the right lateral and left lateral positions, applying to both lungs, with the most affected lung area first. Before and after the procedure, vital signs, blood gas parameters were measured and the amount of secretion collected during the aspiration process was weighed.
expiratory rib cage compression
Expiratory rib cage compression: The hands are placed on the lower third of the rib cage. During expiration, the end and sides of the patients' rib cage are gradually compressed with the hands.At the end of expiration, compression is released from the thorax to allow patients to take a free inspiration. After each compression, the patient is allowed to perform 3 breathing cycles.Expiratory rib cage compression is applied for 5 minutes.
percussion vibration group
Percussion, vibration process stage; Three hours after the first aspiration data were obtained, before the second aspiration, percussion and vibration were applied 3-5 times to each area, starting from the right and left lower lobes, in the right lateral and left lateral positions, with the most affected lung area being applied to both lungs first. Vital signs, blood gas parameters were measured before and after the procedure, and the amount of secretion collected during the aspiration process was weighed.
percussion vibration
Percussion :Percussion is performed 3-5 times on each area from a height of approximately 10 cm with the domed hand. . It starts from the right and left lower lobes and goes up.Vibration:The hand is firmly/strongly placed on the application area. The arm and shoulder are stretched and the fingers are gently vibrated or shaken gently. While the patient is exhaling, vibration is performed 3-5 times in each area, starting from the right and left lower lobes.
control group
Control group phase; In this group, vital signs, blood gases, and secretion amount were recorded at the same time as the experimental groups, without any intervention.
No interventions assigned to this group
Interventions
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expiratory rib cage compression
Expiratory rib cage compression: The hands are placed on the lower third of the rib cage. During expiration, the end and sides of the patients' rib cage are gradually compressed with the hands.At the end of expiration, compression is released from the thorax to allow patients to take a free inspiration. After each compression, the patient is allowed to perform 3 breathing cycles.Expiratory rib cage compression is applied for 5 minutes.
percussion vibration
Percussion :Percussion is performed 3-5 times on each area from a height of approximately 10 cm with the domed hand. . It starts from the right and left lower lobes and goes up.Vibration:The hand is firmly/strongly placed on the application area. The arm and shoulder are stretched and the fingers are gently vibrated or shaken gently. While the patient is exhaling, vibration is performed 3-5 times in each area, starting from the right and left lower lobes.
Eligibility Criteria
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Inclusion Criteria
* Intubated in the intensive care unit for more than 48 hours
* Followed in synchronized intermittent mechanical ventilation (SIMV) mode
* with arterial catheter
* with hemodynamic stability
* PEEP \<10
* Patients with Glasgow Coma Scale \>3 were included.
Exclusion Criteria
* with pneumothorax
* with hemoptysis
* with increased intracranial pressure
* Having a history of spine surgery
* with chest drainage tube
* Those with skin infection and subcutaneous emphysema in the back and chest area
* The mechanical ventilation setting to be changed during the study
* with life-threatening cardiac arrhythmia
* pregnant
* Obese (Body Mass Index \>30)
* Patients who had to be aspirated outside of the specified periods during the study were excluded from the study
18 Years
ALL
No
Sponsors
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Inonu University
OTHER
Responsible Party
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Serap Parlar Kılıç
Proffessor
Locations
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Tunceli State Hospital
Tunceli, , Turkey (Türkiye)
Countries
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Other Identifiers
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2021/1916
Identifier Type: -
Identifier Source: org_study_id
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