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

Sponsor
Eskisehir Osmangazi University (Other)
Overall Status
Completed
CT.gov ID
NCT05186844
Collaborator
(none)
1
1
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Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: survey application

Detailed 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

Study Type:
Observational [Patient Registry]
Actual Enrollment :
1 participants
Observational Model:
Other
Time Perspective:
Other
Official Title:
Posttraumatic Stress Disorder in Parents and Children After Discharge From the Pediatric Intensive Care Unit
Actual Study Start Date :
Jan 1, 2019
Actual Primary Completion Date :
Mar 1, 2019
Actual Study Completion Date :
Jan 20, 2020

Outcome Measures

Primary Outcome Measures

  1. application of the post-traumatic stress disorder scale [on day 0-3 of discharge]

    post traumatic stress disorder scale applied to children

  2. application of the post-traumatic stress disorder scale [on day 0-3 of discharge]

    post traumatic stress disorder scale applied to parents

Secondary Outcome Measures

  1. application of the post-traumatic stress disorder scale [on day 30-40 of discharge]

    post traumatic stress disorder scale applied to children

Other Outcome Measures

  1. application of the post-traumatic stress disorder scale [on day 30-40 of discharge]

    post traumatic stress disorder scale applied to parents

Eligibility Criteria

Criteria

Ages Eligible for Study:
8 Years to 12 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • The child was between 8-12 years old,

  • The child had an accompanying adult present,

  • The child was conscious and/or able to communicate verbally,

  • The child did not have any intellectual disability,

  • There were no challenges in communicating with the family and/or the child (i.e., they spoke Turkish, were able to communicate),

  • The child's stay at the PICU was no longer than 29 days,

  • The child and their family volunteered to participate in the study.

Exclusion Criteria:
  • All participants who do not meet the inclusion criteria

Contacts and Locations

Locations

Site City State Country Postal Code
1 Aysegul Ankara Mamak Turkey 06100

Sponsors and Collaborators

  • Eskisehir Osmangazi University

Investigators

  • Principal Investigator: ayşegül karaca, aysegulkaraca_88@hotmail.com

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ayşegül Karaca, Nurse, Eskisehir Osmangazi University
ClinicalTrials.gov Identifier:
NCT05186844
Other Study ID Numbers:
  • Study1
  • Ayfer Açıkgöz
First Posted:
Jan 11, 2022
Last Update Posted:
Jan 11, 2022
Last Verified:
Dec 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ayşegül Karaca, Nurse, Eskisehir Osmangazi University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 11, 2022