Pain, crying time due to blood sampling, physiological symptoms (heart rate, respiration rate, and oxygen saturation).
Conditions
Interventions
Intervention 1: Intervention group: In the mother's embrace group, the infants are placed in their mother's arms two minutes before, during and at least 15 seconds after blood sampling, with the diffe
Sponsors
Kerman University of Medical Sciences
Eligibility
Sex/Gender
All
Age
266 Days to 294 Days
Inclusion criteria
Inclusion criteria: Healthy full-term infants (38 to 42 weeks) Birth weight 2500-4000 grams Apgar more than 7 at birth. Stability in terms of clinical condition infants at 4th to 6th birthday who to screen for hypothyroidism.
Exclusion criteria
Exclusion criteria: Having any congenital and chromosomal anomalies Having painful interventions such as circumcision and getting the peripheral vein before referring to the health center
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The initial outcome could be an increase or decrease in the pain score. Timepoint: The pain score measurement is done at the beginning of the study (before the intervention), immediately after blood sampling, and 5 minutes after blood sampling. Method of measurement: Neonatal Infant Pain Scale (NIPS).;The initial outcome could be an increase or decrease in the baby's crying time. Timepoint: The time interval for the measurement of the crying time is after blood sampling. Method of measurement: Stop watch. | — |
Secondary
| Measure | Time frame |
|---|---|
| The initial outcome could be an increase or decrease in the heart rate. Timepoint: Heart rate measurement as a secondary outcome is done at the beginning of the study (before the intervention), immediately after blood sampling, and 5 minutes after blood sampling. Method of measurement: Pulse Oximeter.;The initial outcome could be an increase or decrease in SPO2. Timepoint: SPO2 measurement as a secondary outcome is? done at the beginning of the study (before the intervention), immediately after blood sampling, and 5 minutes after blood sampling. Method of measurement: Pulse Oximeter.;The initial outcome could be an increase or decrease in respiratory rate. Timepoint: Respiratory rate measurement as a secondary outcome is done at the beginning of the study (before the intervention), immediately after blood sampling, and 5 minutes after blood sampling. Method of measurement: Pulse Oximeter. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAtefe Roshanray
Kerman University of Medical Sciences
Outcome results
None listed