Audiovisual Interactive Games to Alleviate Pediatric Perioperative Anxiety
Study Details
Study Description
Brief Summary
Pediatric anxiety upon induction of anesthesia is widely prevalent and can lead to negative patient psychological impact and hindrance to induction of anesthesia. Historically, premedication has been used as one means to improve pediatric preoperative anxiety and cooperation with induction. However, giving medication to children prior to surgery has drawbacks. Thus, other means have been proposed that may have similar benefits but fewer or different drawbacks. Recently, audiovisual distraction in the form of interactive games has been proposed. Such games have been in use at children's hospitals around the United States for more than five years. This study is a randomized trial that will explore using interactive games to improve pediatric perioperative anxiety in elective surgery compared with standard-of-care not including games. Perioperative anxiety with be evaluated using an observational scale.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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N/A |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Interactive Gaming Group Subjects will utilize an interactive gaming platform via the Bedside Entertainment and Relaxation Theater (BERT) directly prior to and during induction of anesthesia. |
Device: Bedside Entertainment and Relaxation Theater (BERT)
BERT is a Nebula Capsule Max portable projector that creates a familiar theater experience designed for children to divert attention away from procedures. It is fitted with a remote control that can be utilized to manage on-screen activities. BERT can be used with any wall, ceiling, or projector screen to create the theater experience with a large screen. It can also be used with assist devices, such as steering wheel and noise-canceling headphones.
Other Names:
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| No Intervention: Standard of Care Subjects will be offered standard of care interventions to improve preoperative anxiety. The interactive gaming system under investigation will not be available to this group. |
Outcome Measures
Primary Outcome Measures
- Patient Anxiety assessed by Modified Yale Perioperative Anxiety Score (mYPAS) [Baseline, At Induction of Anesthesia (approximately 1 hour after baseline)]
The mYPAS is the gold standard for measuring pediatric perioperative anxiety. It is an observational-based 22-item instrument divided into five categories: activity, emotional expressivity, state of arousal, vocalization, and use of parents. The score ranges from 23 to 100, higher scores suggest higher levels of anxiety. It was developed at Yale University. This will be used for patients only.
Secondary Outcome Measures
- Caretaker Anxiety assessed by Short State Anxiety Inventory Score [Baseline, After Induction of Anesthesia (approximately 1 hour after baseline)]
The Short State Anxiety Inventory is a 6-item validated measure of anxiety in subjects aged 5 years and older. Subjects are asked to rate how they felt on a 4-point Likert scale in relation to feeling calm, tense, upset, relaxed, content, or worried. A score of 1 correlates to "not at all" and a score of 4 correlates to "very much." The final score is the sum of recorded values and ranges from 6 to 24, higher scores suggest higher levels of anxiety. This will be used for caretakers only.
- Healthcare Professional Opinions on BERT assessed with Health Professional Survey [During first 10 study days]
This survey will obtain health care providers' opinions on the usefulness of using the BERT system in reducing anxiety and the feasibility of such a program in a health care setting. Eligible individuals include: physicians, physician assistants/advanced practice providers, nurses, and other operating room staff.
- Patient induction compliance assessed by Induction Compliance Checklist [At Induction of Anesthesia]
The Induction Compliance Checklist is a validated 10-item observer-rated checklist of behaviors that interfere with induction of anesthesia. The score is the sum of the items checked. A perfect induction (the child does not exhibit negative behaviors, fear, or anxiety) is scored as 0, whereas the worst induction is a score of 9. A score greater than six is considered "poor" compliance
Eligibility Criteria
Criteria
Inclusion Criteria:
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4 to 14 years of age;
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Undergoing non-emergent surgery at Yale New Haven Children's Hospital requiring general anesthesia;
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Chooses inhalational induction as induction method;
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Surgery qualified under one or more of the following fields: otolaryngology, ophthalmology, orthopedics, dentistry, gastrointestinal, general surgery
Exclusion Criteria:
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Altered mental status;
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Significant audiovisual deficits (per parent report and at discretion of study team);
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Received pharmacologic premedication
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Yale New Haven Children's Hospital | New Haven | Connecticut | United States | 06510 |
Sponsors and Collaborators
- Yale University
Investigators
- Principal Investigator: Anthony Longhini, MD, Yale University School of Medicine, Department of Anesthesiology
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 2000033851
- No NIH funding