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Recruiting NCT06250816

The Effects of Wearing Operation Gown With Cartoon Characters on Reducing Preoperative Anxiety in Children: Randomized Controlled Study

No phase Interventional Anxiety, Preoperative

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: The hospital gown with cartoon characters.
Who it may be relevant to
Registry conditions: Anxiety, Preoperative. Basic parameters: 4 years — 12 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The operating room environment can be frightening for pediatric patients. Many techniques have been used to make the operating room environment less intimidating, including allowing parents to accompany part of this procedure, play therapy and various distraction strategies during the entrance to the operating room. In a survey study, it was reported that parents were expected to create hospital conditions with a more child-friendly atmosphere. In this context, it is thought that creating a warmer environment for children, including the clothes worn in the operating room, may reduce the anxiety level of children. In this study, investigators' aim was to investigate the effect of wearing an hospital gown with cartoon characters on the reduction of preoperative anxiety in children scheduled for Orthopedic surgery by in the operating room.

Detailed description

Pediatric patients aged between 4-12 years, who are planned to be operated by the Orthopedic Surgery Clinic in Bursa Uludag University Faculty of Medicine Hospital Surgical Theatre, will be randomized preoperatively by closed envelope method. One group will have a preoperative visit, the investigator will meet the patient and assess the child's anxiety level using the modified Yale Preoperative Anxiety Scale (m-YPAS). Afterwards, the patient will be asked to choose one of the hospital gowns they want to wear and put it on with parental assistance. The other group also will have a preoperative visit, the investigator will meet the patient and assess the child's anxiety level using m-YPAS. The patient will be asked to wear the hospital gown used in the hospital in routine practice with parental assistance. Then the patients will be taken to the operating room as in the routine procedure. Before induction of anesthesia in the operating room, another investigator will re-evaluate the child's anxiety level using the m-YPAS scale. Vital signs, analgesic use and duration of surgery will be recorded during the operation. Afterwards, the satisfaction level of the parents will be evaluated.

Interventions

  • Other The hospital gown with cartoon characters
    The patient will be asked to choose one of the hospital gowns with cartoon characters they want to wear and put it on with parental assistance.

Primary outcome measures

  • modified Yale Preoperative Anxiety Scale [Time frame: 1 day]

Eligibility criteria

Inclusion criteria

  • Patients who are planned to have elective orthopedic surgery
  • Patients whose American Society of Anesthesiologists (ASA) physical status classification are between 1-3
  • Patients who have approved the informed consent form

Exclusion criteria

  • Motor and/or mentally retarded patients
  • Patients with hearing-speech impairment
  • Patients whose ASA physical status classification IV-V
  • Patients who do not accept informed consent and/or refused to participate in the study

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Health services research

Study locations

Turkey (Türkiye) · 1 center
  • Uludağ Üniversitesi — Bursa

Identifiers

NCT: NCT06250816 · 2023-28/21

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗