The Effect of Quiet Time Protocol on Physiological in Preterm infants

Phase 2

Completed

• Conditions: preterm infant.; Other preterm infants

• Registration Number: IRCT2013082414454N1
• Lead Sponsor: Vice Chancellor for Research, Mashhad University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 120

Inclusion Criteria

parental consent; infants age between 37-30 weeks; hemodynamic stability (HR=120-160, RR=30-50, SPO2=85%-95% and keep axillary temperature range of 37-36 degrees C); Apgar scores of 7 or more on the first and fifth minutes of Birth; spontaneous ventilation and no need for ventilation; Lack of congenital malformations.
Exclusion criteria: Lack of consent to continue working for any reason; Ventilation during the study need to be; During the study, infants with recurrent Apnea; During the study, neonates with seizures; If the baby is ill and the environmental stimuli exceeded, the day will be removed.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Vital Signs (Blood Pressure, Heart Rate, Respiratory Rate and Saturation O2) before to implementing Quiet Time Protocol. Timepoint: Every 15 minutes to 2 hours. Method of measurement: Heart Rate in beat per minute, Respiratory Rate in number per minute, Saturation O2 in percent and Blood Pressure in milimeter Hg using Monitoring.

Secondary Outcome Measures

Name	Time	Method
Stabilization of Vital Signs (Blood Pressure, Heart Rate, Respiratory Rate and Saturation O2) at implementing Quiet Time Protocol. Timepoint: Every 15 minutes to 2 hours at starting at Quiet Time Protocol. Method of measurement: Heart Rate in beat per minute, Respiratory Rate in number per minute, Saturation O2 in percent and Blood Pressure in milimeter Hg using Monitoring.