Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT06361069 |
Other study ID # |
asliakdeniz |
Secondary ID |
|
Status |
Completed |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
April 1, 2023 |
Est. completion date |
January 1, 2024 |
Study information
Verified date |
April 2024 |
Source |
Bilecik Seyh Edebali Universitesi |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
Aim: This study was conducted to determine the efficacy of finger puppets, distraction cards
and kaleidoscope for reducing anxiety in children undergoing day surgery.
Methods: The study was conducted using the "pre-post test unmatched group model", one of the
quasi-experimental methods. The study was conducted between April 2023 and January 2024 with
children aged 6-12 years who were admitted to the pediatric clinic of a hospital for day
surgery. A total of 85 children (including 20 children in the control group, 22 children in
the finger puppet intervention group, 21 children in the distraction cards intervention
group, and 22 children in the kaleidoscope intervention group) who were hospitalized in the
pediatric clinic between April 2023 and January 2024 and who met the inclusion criteria were
included in the study. Descriptive statistics, Mann Whitney U test, Kruskal Wallis and
regression analysis were used in the evaluation of the data.
Description:
This study was conducted to determine the efficacy of finger puppets, distraction cards and
kaleidoscope for reducing anxiety in children undergoing day surgery. The study was conducted
using the "pre-post test unpaired group model", one of the quasi-experimental methods.
The study was carried out from April 2023 to January 2024, involving children aged 6-12 years
admitted to the pediatric clinic of a teaching and research hospital for day surgery
(tonsillectomy, circumcisio, adenotonsillectomy etc.). Notably, the nursing care provided at
the hospital does not incorporate distraction techniques aimed at alleviating anxiety in
children.
Sample The sample required for the study was calculated using the G*Power (3.1.9.4) computer
program. Based on the Type I error of 5%, Type II error of 99%, SD = 6.20, and Type I error
of 5% in the study by Dehghan et al. (2017), the desired effect size for this study was 0.55
and the total required sample size was 64 children (approximately 21 children for each group)
(Dehghan et al., 2017). A total of 85 children, comprising 20 children in the control group,
22 in the finger puppet intervention group, 21 in the distraction cards intervention group,
and 22 in the kaleidoscope intervention group, was recruited from the pediatric clinic
between April 2023 and January 2024, meeting the study's inclusion criteria. Notably, no
randomization method was employed in the selection process.