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NCT06285669 Clinical Trial

Effects of Kinesiotaping on Respiratory Muscles in Very Preterm Infants

Respiratory Distress Syndrome Clinical Trial

Official title:
Effects of Kinesio Taping Applications on Diaphragm, Respiratory Muscles and Chest Wall In Very Preterm Infants On Non-invasive Ventilation

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06285669
Other study ID # KA18/35
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2018
Est. completion date June 30, 2020

Study information
Verified date February 2024
Source Ondokuz Mayis University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aimed to evaluate the effects of kinesio taping on blood gas parameters, respiratory rate, heart rate, oxygen saturation, and pressure limits in preterm infants with RDS who are on NIV. It is hypothesized that the application of kinesio taping to the chest area of preterm infants may improve respiratory functions and oxygenation at the alveolar level, leading to decreased work of breathing, reduced respiratory rate, and improved neonatal stability by promoting respiratory mechanics and enhancing chest expansion.

Description:

Very preterm infants are at high risk of respiratory distress syndrome (RDS), due to surfactant deficiency and weak respiratory muscles. This condition can contribute to respiratory workload and irregular breathing. This study aimed to investigate the effects of Kinesio kinesio-taping technique on the respiratory muscles and diaphragm in very preterm infants undergoing non-invasive. Twenty-six preterm infants born before the 32nd gestational week and requiring non-invasive ventilation (NIV) support due to RDS, were randomly divided into 2 groups as Kinesio taping group and control group. Kinesio taping was applied by a single physiotherapist to support the intercostal muscles,and, the diaphragm and facilitatory method was used on the respiratory muscles. Kinesio taping was removed just after preterm infants were weaned from noninvasive ventilation. Blood gas parameters, respiratory rate, heart rate, FiO2, FiO2/pO2 ratio, PIP, PEEP values, and length of stay in NIV were recorded before and after 3 days of KT application.

Recruitment information / eligibility
Status Completed
Enrollment 26
Est. completion date June 30, 2020
Est. primary completion date June 30, 2020
Accepts healthy volunteers No
Gender All
Age group 1 Month to 4 Months
Eligibility Inclusion Criteria: - Preterm infants diagnosed with RDS - Preterm Infants born under 32 weeks of gestation Exclusion Criteria: - Sepsis, - necrotizing enterocolitis, - metabolic disease, - severe congenital malformations of the chest and abdominal walls, - congenital heart disease, - major congenital anomalies

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• kinesiotaping application
kinesiotaping application

Locations
Country Name City State
Turkey Nilay Çömük Balci Samsun Atakum

Sponsors (1)
Lead Sponsor Collaborator
Ondokuz Mayis University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Level of pH through study completion, an average of 1 year
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