The Impact of an Animated Video on Preoperative Anxiety in Children Undergoing Elective Otoplasty

Sponsor
IWK Health Centre (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05894187
Collaborator
(none)
40
2
15

Study Details

Study Description

Brief Summary

The study is a prospective, randomized, single-blind controlled superiority trial to evaluate the effect of viewing an informative animated video a day prior to surgery on preoperative anxiety in pediatric patients scheduled for elective otoplasty. The primary outcome will be modified Yale Preoperative Anxiety Scale (mYPAS) score at the time of general anesthesia induction compared between families that were assigned to view the animated video the day before and those that were not. The participants for this study will be children undergoing elective otoplasty at the IWK Health Centre. Those participants randomized to the intervention group will receive a link to a short survey gauging parent anxiety levels. The survey will be followed by a link to an informative animated video which the participants and their families will watch. The control group will be participants assigned not to receive the email link to the informative animated video.

Condition or Disease Intervention/Treatment Phase
  • Other: animated video
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Intervention Model Description:
prospective, randomized, single-blind controlled superiorityprospective, randomized, single-blind controlled superiority
Masking:
Triple (Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Supportive Care
Official Title:
Exploring the Effects of an Informative Animated Video on Preoperative Anxiety in Children Undergoing Elective Otoplasty and Their Parents
Anticipated Study Start Date :
Jun 1, 2023
Anticipated Primary Completion Date :
Jun 1, 2024
Anticipated Study Completion Date :
Sep 1, 2024

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control group (no video)

Children in this group will not receive a link to view an informational animated prior to their surgery date

Experimental: Intervention group ( video)

Children in this group will receive a link to view an informational animated video 3 nights prior to their surgery date.

Other: animated video
Participants randomized to the intervention group will receive a link to a short survey gauging parent anxiety levels three days prior to their childs surgery date. If randomly assigned to watch the informative animated video, the survey will be followed by a link to a video which families are free to watch prior to your child's surgery date. Once participants and there family watch the video, they will be asked to rate the quality of the video on a scale of 0 (very bad) to 10 (excellent). Responses to this question will be used to confirm that participants watched the video to the end.

Outcome Measures

Primary Outcome Measures

  1. modified Yale Preoperative Anxiety Scale (mYPAS) [Data acquisition will occur within 24 hours. Recording will start once patient enters room and is positioned on OR table. Recording will stop one minute after induction mask is put on patient. Total recording time will be five minutes.]

    The mYPAS is a validated observational measure to assess the behaviour of children of all ages preoperatively and consists of 27 items divided into five domains (activity, emotional status, arousal state, vocalization, and use of parents).24,27,28 The mYPAS scores range from 22 to 100, with higher values indicating greater anxiety. The mYPAS is considered the gold-standard for observational preoperative anxiety assessment in paediatric patients.24,27-30

Secondary Outcome Measures

  1. parental self-reported anxiety using the State-Trait Anxiety Inventory [Within 48 hours prior to arrival at the IWK for surgery and again upon arrival at the IWK immediately prior to their child leaving the waiting area to enter the operating room]

    The STAI, which consists of two 20-item subscales measures is self-administered on a four-point scale for each item. The scores for each of the subscales range from a minimum of 20 to a maximum of 80, the higher scores suggest the greater psychological anxiety. The tool was designed to differentiate between the temporary condition of "state anxiety" in response to an acute event and the more general and long-standing quality of "trait anxiety" entrenched in the individual's personality. This tool has been validated in a variety of clinical settings including parental anxiety prior to a child's surgery.26

  2. modified Yale Preoperative Anxiety Scale (mYPAS) [mYPAS score while in the preoperative waiting area]

    The mYPAS is a validated observational measure to assess the behaviour of children of all ages preoperatively and consists of 27 items divided into five domains (activity, emotional status, arousal state, vocalization, and use of parents).24,27,28 The mYPAS scores range from 22 to 100, with higher values indicating greater anxiety. The mYPAS is considered the gold-standard for observational preoperative anxiety assessment in paediatric patients.24,27-30

Eligibility Criteria

Criteria

Ages Eligible for Study:
4 Years to 12 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • They are undergoing an otoplasty alone with no other procedures on the same day

  • The patient must not have previously undergone an otoplasty; the patient must be between the ages of 4 and 12;

  • The patient must understand spoken English;

  • The participating parent must be able to read English at a grade six level; and the patient should not have received premedication.

Exclusion Criteria:
  • Under the age of 4 or over the age of 12

  • Have not undergone a previous otoplasty

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • IWK Health Centre

Investigators

  • Principal Investigator: Michael Bezuhly, MD, IWK Health Centre

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Michael Bezuhly, Head, Division of Plastic & Reconstructive Surgery Director, Craniofacial Program IWK Health Centre, IWK Health Centre
ClinicalTrials.gov Identifier:
NCT05894187
Other Study ID Numbers:
  • 1028283
First Posted:
Jun 8, 2023
Last Update Posted:
Jun 9, 2023
Last Verified:
Jun 1, 2023
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 Michael Bezuhly, Head, Division of Plastic & Reconstructive Surgery Director, Craniofacial Program IWK Health Centre, IWK Health Centre
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 9, 2023