-
Study aim
-
effect of lavender aromatherapy on behavioral reactions of preterm neonates
-
Design
-
The clinical trial has a control group with single-blind, parallel groups, randomized, phase 3, on 86 infants. RANDOM ALLOCATION SOFTWARE will be used for the randomization sequence.
-
Settings and conduct
-
This study will be conducted in the neonatal intensive care unit of Ghaem Hospital in Mashhad. In the intervention group, behavioral reactions will be recorded before the intervention begins. The newborn will be subjected to lavender aromatherapy for one hour. Immediately after the aromatherapy is completed and half an hour later, behavioral reactions will be scored according to the ABSS scale.
-
Participants/Inclusion and exclusion criteria
-
Inclusion criteria:
Neonatal age 28-34 weeks gestation
Under non-invasive ventilation
Having stable vital signs
Apgar score at birth at 5 minutes above 6
No invasive procedure performed on the newborn 2 hours ago
Absence of all types of neonatal anomalies
Informed parental consent.
Exclusion criteria:
Gestational age greater than 34 weeks
Addicted mother,intubated neonate,neonate has nasal cannula, Using narcotics and sedatives
-
Intervention groups
-
In the intervention group, infants will be exposed to lavender aromatherapy for one hour.
Infants will be observed for 30 seconds over two consecutive days, once before the aromatherapy is applied, twice after the aromatherapy begins, once immediately after the aromatherapy ends, and a second time half an hour after the aromatherapy ends, and their behaviors will be recorded using the Anderson behavioral scale.The study will be conducted over two consecutive days from 3:00 PM to 5:00 PM, .In the control group, No scent will be used for this group, and the behavioral response will be examined.
-
Main outcome variables
-
Behavior.