- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05036603
Comparison of the Acute Effects of Chest Physiotherapy Methods Applied in Different Positions in Preterm Newborns (therapy)
September 5, 2025 updated by: Hatice Adiguzel, PT, Sanko University
Infants in the neonatal intensive care unit (NICU) may be lost due to risks such as being sensitive, frequent exposure to birth complications and being prone to infection.
The most common causes of mortality in newborn babies in the world; Complications due to preterm delivery (28%), infections (26%) and perinatal asphyxia (23%) were reported.
Respiratory problems are observed in 4-6% of newborns.
These problems are also important causes of mortality in the neonatal period.
Newborn infants are more likely to have respiratory distress due to difficulties in airway calibration, few collateral airways, flexible chest wall, poor airway stability, and low functional residual capacity.Invasive mechanical ventilation (IMV) is frequently used in the treatment of newborns with respiratory failure.
Various ventilation modes and strategies are used to optimize mechanical ventilation and prevent ventilator-induced lung injury.
Among the important issues to be considered in newborns connected to mechanical ventilator (MV); Choosing an appropriately sized endotracheal tube to reduce airway resistance and minimize respiratory workload, correct positioning, regular nursing care, chest physiotherapy, sedation-analgesia, and infection prevention are also included.
Study Overview
Status
Completed
Conditions
- Preterm Birth
- Respiratory Distress Syndrome
- Bronchopulmonary Dysplasia
- Mechanical Ventilation Complication
- Chronic Liver Disease
- Hyaline Membrane Disease
- Premature
- Oxygen Toxicity
- Neonatal Respiratory Failure
- Atelectasis Neonatal
- Mechanical Ventilation Pressure High
- Pneumonia Neonatal
- Lobar Collapse
Intervention / Treatment
Detailed Description
Infants in the neonatal intensive care unit (NICU) may be lost due to risks such as being sensitive, frequent exposure to birth complications and being prone to infection.
The most common causes of mortality in newborn babies in the world; Complications due to preterm delivery (28%), infections (26%) and perinatal asphyxia (23%) were reported.
Respiratory problems are observed in 4-6% of newborns.
These problems are also important causes of mortality in the neonatal period.
Newborn infants are more likely to have respiratory distress due to difficulties in airway calibration, few collateral airways, flexible chest wall, poor airway stability, and low functional residual capacity.Invasive mechanical ventilation (IMV) is frequently used in the treatment of newborns with respiratory failure.
Various ventilation modes and strategies are used to optimize mechanical ventilation and prevent ventilator-induced lung injury.
Among the important issues to be considered in newborns connected to mechanical ventilator (MV); Choosing an appropriately sized endotracheal tube to reduce airway resistance and minimize respiratory workload, correct positioning, regular nursing care, chest physiotherapy, sedation-analgesia, and infection prevention are also included.The preference for using non-invasive mechanical ventilation (NIMV) modes in NICUs is also increasing.
Despite this, the use of IMV is still often required in preterm infants in the need for respiratory support and in the treatment of respiratory failure.
Today, extremely preterm infants are extubated quickly.
Because prolonged IMV can be a very important risk factor in the development of Bronchopulmonary Dysplasia (BPD).
The reason for this is the physiological characteristics of newborns such as airway maintenance and cleanliness, smaller airway calibration, reduction in collaterals, flexible chest wall, poor airway stability, and low functional residual capacity.
A small amount of secretion in preterm infants can produce a large increase in airway resistance.
This reduces airflow and without expiratory flow, secretions cannot be expelled.
With chest physiotherapy (CP), adequate expiratory flow can be achieved without causing airway closure.Chest physiotherapy techniques (CP) create mechanical effects in the lung, increasing ventilation, facilitating the removal of secretions and preventing bronchial obstruction.
This ensures correct protection of the airways and facilitates extubation.
Prolonged intubation and increased length of stay in NICUs can also lead to complications such as atelectasis, respiratory infections and chronic lung disease.
Decreased oxygenation and excessive accumulation of secretions cause widespread increase in airway resistance, leading to prolonged ventilation or oxygen support.
Oxygen therapy is an integral part that is frequently used as respiratory support in NICUs.
However, long-term oxygen therapy may cause excessive accumulation of bronchial secretions.
This makes CP mandatory.
Traditional CP has become an indispensable part of airway management in NICU settings to remove excess bronchial secretions and thereby increase oxygenation.
There are many studies on CP in the literature.In some of these studies, it was found that it did not prevent atelectasis, that CP had no effect, or that CP accelerated weaning from MV.
The role of CP in reducing respiratory morbidity in infants and neonates continues to be debated and more studies are needed.
CP needs to be supported by well-controlled studies with large sample sizes, particularly regarding the techniques used and specific protocols.
Therefore, in this study, it is aimed to compare the acute effects of CP methods applied in different positions in preterm newborns.
Study Type
Interventional
Enrollment (Actual)
60
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
-
-
-
Kahramanmaraş, Turkey (Türkiye), 46100
- Kahramanmaraş Sütçü İmam 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
1 day to 1 month (Child)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Preterm newborns born <37 and >28 weeks due to MV or CPAP, hospitalized in the NICU and with a voluntary consent form from their families (with segmental lobar collapse as a result of Chest X-Ray, RDS/BPD/HMH/Atelectasis/Pneumonia/ Preterm newborns diagnosed with Chronic Pulmonary Disease or in stable condition with a thick and secretory focus on X-ray)
- First-time infants who have not received any chest physiotherapy program
Exclusion Criteria:
Newborn infants who have been unstable in the last 2 days (SpO₂ <60 mmHg, heart rate, blood pressure, persistent apnea, excessive increases in respiratory rate, tachycardia, nasal wing breathing, cyanosis..etc)
- Newborn infants with rib fracture, hemoptysis, diaphragmatic hernia, pulmonary hemorrhage, pneumothorax
- Those diagnosed with any known heart disease or genetic disease
- Those with osteopenia-osteoporosis or thrombocytopenia
- Infants with any known neurological diagnosis (Abnormal MRI finding, Hydrocephalus, Chiari Malformation, Asphyxia, Periventricular Leukomolacia (PVL), Intraventricular Hemorrhage (IVH), Kernicterius, Hypoxic Ischemic Encephalopathy (HIE), Hydrocephalus)
- Preterm infants weighing <1000 g
- Infants born with congenital anomaly (Spina Bifida, Arthrogryposis Multiplex Congenita..etc)
- Newborns undergoing any surgery
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: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: 1/routin medical care and neonatal intensive care unit's daily care
Group 1 (n=20) routine medical treatment for newborns on mechanical ventilator respiratory support and CPAP; Appropriate antibiotics given according to the needs of the baby, enteral-parenteral nutrition, oral or nebulizer drugs for softening the secretion, vitamin supplements and routine nursing care will be provided.
|
|
|
Experimental: 2/active chest physiotherapy in modified drainage positions
Group 2 (n=20) newborns on mechanical ventilator respiratory support and CPAP; A single session of active chest physiotherapy (CP) will be applied using modified drainage positions (avoiding the trendelenburg position, excessive position change and avoiding hand contact in babies younger than 30 weeks or who are sensitive to position change).
Active CP in various modified drainage positions; It will consist of percussion and vibration methods with proprioceptive replacement stimulations.
After these methods, aspiration will be performed and a suitable position will be given to the lobe that is desired to be ventilated.
In addition, these patients will be given routine medical treatment consisting of appropriate antibiotics, enteral-parenteral nutrition, oral or nebulizer drugs for softening the secretion, vitamin supplements and routine nursing care.
|
diffferent chest physiotherapy methods
|
|
Experimental: 3/active chest physiotherapy in prone positions
Group 3 (n=20) newborns on mechanical ventilator respiratory support and CPAP; a single session of active chest physiotherapy treatment to be applied only in the prone position; Starting with proprioceptive stimulation, percussion and vibration methods will be applied.
After these methods, aspiration will be performed and a suitable position will be given to the lobe that is desired to be ventilated.
In addition, these patients will be given routine medical treatment consisting of appropriate antibiotics, enteral-parenteral nutrition, oral or nebulizer drugs for softening the secretion, vitamin supplements and routine nursing care.
|
diffferent chest physiotherapy methods
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
heart rate
Time Frame: Before starting chest physiotherapy and up to15 minutes after ending therapy
|
heart rate of the preterm newborns
|
Before starting chest physiotherapy and up to15 minutes after ending therapy
|
|
chest X-Ray
Time Frame: on the 1st day before starting chest physiotherapy session and up to 24 hours after chest physiotherapy session
|
chest X-Ray of the preterm newborns
|
on the 1st day before starting chest physiotherapy session and up to 24 hours after chest physiotherapy session
|
|
arterial blood gases
Time Frame: on the 1st day before starting chest physiotherapy session and up to 24 hours after chest physiotherapy session
|
arterial blood gases from the radial artery or from the umbilical catheter in infants with an umbilical catheter
|
on the 1st day before starting chest physiotherapy session and up to 24 hours after chest physiotherapy session
|
|
PaO₂
Time Frame: on the time before starting chest physiotherapy and up to 15 minutes after ending therapy
|
PaO₂ of the preterm newborns
|
on the time before starting chest physiotherapy and up to 15 minutes after ending therapy
|
|
blood pressure
Time Frame: on the time before starting chest physiotherapy and up to15 minutes after ending therapy
|
blood pressure of the preterm newborns
|
on the time before starting chest physiotherapy and up to15 minutes after ending therapy
|
|
respiratory rate
Time Frame: Before starting chest physiotherapy and up to15 minutes after ending therapy
|
respiratory rate of the preterm newborns
|
Before starting chest physiotherapy and up to15 minutes after ending therapy
|
|
Peep (cm H₂O)
Time Frame: on the time before starting chest physiotherapy and up to 15 minutes after ending therapy
|
Peep (cm H₂O) of the preterm newborns
|
on the time before starting chest physiotherapy and up to 15 minutes after ending therapy
|
|
Pip (cm H₂O)
Time Frame: on the time before starting chest physiotherapy and up to15 minutes after ending therapy
|
Pip (cm H₂O) of the preterm newborns
|
on the time before starting chest physiotherapy and up to15 minutes after ending therapy
|
|
FİO₂ (%/mm Hg)
Time Frame: on the time before starting chest physiotherapy and up to 15 minutes after ending therapy
|
FİO₂ (%/mm Hg) of the preterm newborns
|
on the time before starting chest physiotherapy and up to 15 minutes after ending therapy
|
|
O₂ Saturation (mmHg) (SpO₂)
Time Frame: on the time before starting chest physiotherapy and up to 15 minutes after ending therapy
|
O₂ Saturation (mmHg) (SpO₂) of the preterm newborns
|
on the time before starting chest physiotherapy and up to 15 minutes after ending therapy
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Chest shape and type (barrel/pektusexcavatum..etc)
Time Frame: on the time before starting chest physiotherapy and up to 15 minutes after ending therapy
|
Chest shape and type (barrel/pektusexcavatum..etc) will be noted by inspection before and after chest physiotherapy.
|
on the time before starting chest physiotherapy and up to 15 minutes after ending therapy
|
|
Respiratory stress
Time Frame: before physiotherapy
|
The chest will be inspected before physiotherapy to note any signs of respiratory stress (chest retraction, expiratory sound, wheezing, etc.) and skin color (cyanosis/pink-bright-vivid/pale-white).
|
before physiotherapy
|
|
the respiratory pattern
Time Frame: on the time before starting chest physiotherapy and up to 15 minutes after ending therapy
|
Before and after chest physiotherapy, the physiotherapist will evaluate the respiratory pattern (tachypnea, periodic breathing, apnea, coughing, sneezing) by inspection.
|
on the time before starting chest physiotherapy and up to 15 minutes after ending therapy
|
|
Daily nutrition type
Time Frame: on the time before starting chest physiotherapy and up to 24 hours after chest physiotherapy
|
Daily nutrition type will be learned and respiratory problems encountered during feeding will be learned from the nurse/mother and noted.
|
on the time before starting chest physiotherapy and up to 24 hours after chest physiotherapy
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: hatice Adiguzel, PhD, Kahramanmaraş Sütçü İmam University
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)
April 1, 2022
Primary Completion (Actual)
July 30, 2024
Study Completion (Actual)
December 15, 2024
Study Registration Dates
First Submitted
August 18, 2021
First Submitted That Met QC Criteria
September 1, 2021
First Posted (Actual)
September 5, 2021
Study Record Updates
Last Update Posted (Estimated)
September 12, 2025
Last Update Submitted That Met QC Criteria
September 5, 2025
Last Verified
August 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Obstetric Labor, Premature
- Obstetric Labor Complications
- Pregnancy Complications
- Respiratory Tract Diseases
- Lung Diseases
- Respiration Disorders
- Infant, Premature, Diseases
- Infant, Newborn, Diseases
- Lung Injury
- Ventilator-Induced Lung Injury
- Respiratory Distress Syndrome, Newborn
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Premature Birth
- Respiratory Distress Syndrome
- Pulmonary Atelectasis
- Bronchopulmonary Dysplasia
- Hyaline Membrane Disease
Other Study ID Numbers
- FTR
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
there is no plan to make individual participant data (IPD) available to other researchers.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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