The effect of combined non-pharmacological interventions on venous blood sampling pain in preterm infants: a clinical trial study
Not Applicable
- Conditions
- sing non-pharmacological interventions to reduce the pain of newborns.
- Registration Number
- IRCT20200913048704N3
- Lead Sponsor
- Babol University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 88
Inclusion Criteria
Premature infants with a gestational age of 32 to 36 weeks and six days
Stability of vital signs before sampling
No congenital or genetic abnormalities
Non-use of drugs, antidepressants and anticonvulsants by the mother during pregnancy
No surgery and receiving anesthesia and anesthesia drugs
Lack of intubation
Exclusion Criteria
Abnormalities in the head and skull such as cleft lip and palate and atrial fibrillation
Infants who experience more than grade II intraventricular hemorrhage during the study
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intensity of pain during venous blood sampling in infants. Timepoint: Before blood collection, during blood collection, 15 minutes after blood collection. Method of measurement: Premature infant pain profile.
- Secondary Outcome Measures
Name Time Method Physiological changes of newborns during and after venous blood sampling. Timepoint: Before the intervention, during the intervention and 15 minutes after the intervention. Method of measurement: Use of cardiorespiratory monitoring device.