Viewing Study NCT06642285



Ignite Creation Date: 2024-10-26 @ 3:42 PM
Last Modification Date: 2024-10-26 @ 3:42 PM
Study NCT ID: NCT06642285
Status: RECRUITING
Last Update Posted: None
First Post: 2024-10-09

Brief Title: Effect of Implementing Evidence Based Practices on Prevention of Associated Nasal Pressure Injuries Among Preterm Neonates With Non-Invasive Respiratory Support
Sponsor: None
Organization: None

Study Overview

Official Title: Effect of Implementing Evidence Based Practices on Prevention of Associated Nasal Pressure Injuries Among Preterm Neonates With Non-Invasive Respiratory Support
Status: RECRUITING
Status Verified Date: 2024-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study aims to evaluate the effect of implementing evidence based practices on prevention of associated nasal pressure injuries among preterm neonates with non invasive respiratory support
Detailed Description: The researchers explained the studys aim benefits and procedures for participation after that the parents of the neonates provided an informed consent Over a one-week period staff education programs regarding Evidence-Based Guidelines for non-invasive respiratory support will be conducted for NICU nursing staff These sessions lasting 15 to 20 minutes will be held during regularly scheduled work hours with four different sessions will offer throughout the day The preterm neonates characteristics and clinical data will be extracted from their hospital records for the two groups on the first day of admission for both groups prior to intervention to identify those who fulfilled the current studys inclusion criteria Neonatal baseline data was collected from their records on the first day of admission for the two groups prior to intervention in order to identify neonates who meet the required criteria of the study Then the participants were selected and divided randomly using a simple random method into two equal groups One subject for the control group one for the study group and so on distributed the participants into two equivalent groups as fellow

Control Group Consisted of 30 premature neonates who will receive conventional hospital care with no additional interventions

Study Group Consisted of 30 premature neonates who will receive 6 evidence-based practices on the prevention of nasal pressure injuries as follows

Use an appropriately sized nasal interface device
The Use of Skin Barrier Products between nasal skin and nasal interface device
Visually examining the preterm newborn every hour to ensure appropriate nasal interface position
Once every 12-hour shift the protective barrier and nasal device are briefly removed to allow for a full nasal skin examination
Follow developmental care principles by repositioning the infant every three to four hours
Pain scores should be taken at least every three to four hours

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None