All stages of the research were carried out after obtaining informed consent from parents and obtaining permission from the vice chancellor of the Babol University of Medical Sciences and the Code of Warm compress,
Conditions
Interventions
Experimental Procedure/Surgery,Experimental Procedure/Surgery
Sponsors
none
Eligibility
Sex/Gender
All
Age
1 Weeks to 37 Weeks
Inclusion criteria
Inclusion criteria: 1) age of at least 37 weeks; 2) auditory health by checking the startle test (jumping); 3) congenital anomalies such as cleft palate; 4) lack of experience in other pain reliever procedures before intervention; 5) observing the interval of at least one hour until intervention.
Exclusion criteria
Exclusion criteria: 1) lack of informed consent of the parents or the desire to withdraw at each stage of the study; 2) receiving any sedative and anti-convulsion drugs; 3) any abnormalities in the head and skull; and 4) failure in heel-blood sampling in first time.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| pain 2-week Neonatal Infant Acute Pain Assessment Scale | — |
Secondary
| Measure | Time frame |
|---|---|
| heart rate changes 2-week manual | — |
Countries
iran
Contacts
Public Contactbijan pirnia
Bijan Center
Outcome results
None listed