About this trial
The study was planned to be conducted and completed within 6 months after ethics committee approval was obtained. The research is a prospective, quasi-experimental study.
The population of the study will consist of children hospitalized in the Pediatric Intensive Care Unit of SBU, Izmir Dr. Behçet Uz Pediatric Diseases and Surgery Training and Research Hospital. Randomization of children will be done to determine which children's data will be followed on the relevant visit day.
Physiologic parameters including respiratory rate, pulse rate, oxygen saturation, body temperature, blood pressure and comfort levels of the children will be evaluated just before, during and after the parental visit (1st minute and 5th minute) and compared with those before the parental visit. All observations will be made by the same nurse to avoid bias in the study.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Being hospitalized in Behçet Uz Pediatric Intensive Care Unit
Parent's volunteering to participate in the study
Disqualifiers
None
Trial population
0-3 years
Trial design
Case-only
Prospective
Treatments tested in this trial
parental presence
Behavioralparental presence in PICU
Treatment groups
Trial outcomes
Primary outcomes
comfort scale point
before, during and after the 1st and 5th minute of the visit
Secondary outcomes
heart rate
heart rate will be measured by Braun YK-81CEU
saturation
saturation will be measured by Braun YK-81CEU
respiratory rate
respiratory rate will be measured by Braun YK-81CEU
blood pressure
blood pressure will be measured by Nimo HS-20C Aneroid
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Izmir Katip Celebi University
Lead sponsor
Dr. Behcet Uz Children's Hospital
Collaborator
This trial is not recruiting at the moment. You can still explore other options: