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Posttraumatic Stress Disorder in Parents and Children After Discharge From the Pediatric Intensive Care Unit — PTSD  

Posttraumatic Stress Disorder Clinical Trial

Official title:
Posttraumatic Stress Disorder in Parents and Children After Discharge From the Pediatric Intensive Care Unit

Clinical Trial Summary

Background: If disorders that occur immediately after a trauma are not treated, they may become chronic and turn into severe health problems. Objectives: This study was conducted with children who had spent time in an intensive care unit and their parents to examine the development of posttraumatic stress disorder (PTSD) in both children and parents. Methods: The study was a cross-sectional study. A total of 110 children, 98 mothers and 80 fathers were included in the study.

Clinical Trial Description

Background: If disorders that occur immediately after a trauma are not treated, they may become chronic and turn into severe health problems. Objectives: This study was conducted with children who had spent time in an intensive care unit and their parents to examine the development of posttraumatic stress disorder (PTSD) in both children and parents. Methods: The research was carried out in the intensive care unit of a children's hospital in Turkey. Children between the ages of 8-12 who had spent time in the PICU over the period January 1 - March 1, 2019, who had been discharged from the PICU or transferred into another unit during this time, and who met the research criteria were included in the study. Between these dates, the total number of children discharged from intensive care or transferred into another unit was 166. Of these children, 138 were between the ages of 8-12. During this period, three children who died, two children whose general condition meant they were unable to participate in the study, and 23 children for whom parental consent could not be obtained were excluded from the study. The study was ultimately completed with 110 children. In addition, the parents of the children in the sample group (98 mothers and 80 fathers) who were alive, reachable, and who agreed to participate were included in the study. Results: A total of 110 children, 98 mothers and 80 fathers who agreed to participate in the study, met the sample selection criteria, and were available throughout were included in the study. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05186844
Study type Observational [Patient Registry]
Source Eskisehir Osmangazi University
Contact
Status Completed
Phase
Start date January 1, 2019
Completion date January 20, 2020
View Details
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