The Effect of Position Change on Pain and Cerebral Oxygen Saturation

Medipol Health Group

Status

Completed

Conditions

Children

Treatments

Other: Positioning

Study type

Interventional

Funder types

Other

Identifiers

NCT06622330

E-15916306-604.01.01-209306724

Details and patient eligibility

About

This study is a randomized controlled experimental study to investigate the effect of position change on pain and cerebral oxygen saturation after endotracheal aspiration in pediatric patients.

Full description

This study is a randomized controlled experimental study to investigate the effect of position change on pain and cerebral oxygen saturation after endotracheal aspiration in pediatric patients. The study sample consisted of 70 pediatric patients (35 in the control group and 35 in the intervention group) who met the inclusion criteria and whose parents gave informed consent. The research data were collected using the "Child Identification Form" and the "Behavioral Pain Scale". SPSS 24 program was used to analyze the data obtained in the study. Children in the experimental group were given 30 minutes of wrapping and 30 minutes of fetal position after aspiration. Children in the control group did not receive any treatment.

Enrollment

70 patients

Sex

All

Ages

1 month to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Pediatric patients whose consent form is signed by their legal guardian
Intubated pediatric patients receiving mechanical ventilation support
Non-sedatized pediatric patients
Pediatric patients who have received only paracetamol and whose duration of action has exceeded 4-6 hours

Exclusion criteria