Actively Recruiting

Phase Not Applicable
Age: 8Years - 13Years
All Genders
NCT02687243

StoryTelling Medicine Application Using a Virtual Reality Intervention

Led by McMaster University · Updated on 2024-12-02

118

Participants Needed

1

Research Sites

319 weeks

Total Duration

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AI-Summary

What this Trial Is About

Preoperative anxiety (PA) affects up to 5 million children in North America each year and is associated with adverse medical, psychological, and behavioral effects. Children who are highly anxious often require more medications during surgical procedures and take longer to recover. While many attempts have been made to reduce PA in children, existing interventions are limited by their expense and time intensive nature. Thus, the current lack of effective and efficient methods of reducing anxiety in children before and after surgery has prompted us to develop and propose to test a new intervention. The investigators have developed a novel,interactive tablet based Virtual Reality program, StoryTelling Medicine (STM), to help reduce anxiety in children undergoing elective surgery, and its associated negative effects. STM is an age appropriate, customizable program to prepare children for complex surgical procedures by guiding them through the hospital settings. The investigators will examine if STM is effective in reducing PA and its adverse effects in children undergoing surgery. If effective, STM has the potential to improve children's and families' surgical experiences, and reduce health problems in the hospital setting and beyond.

CONDITIONS

Official Title

StoryTelling Medicine Application Using a Virtual Reality Intervention

Who Can Participate

Age: 8Years - 13Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Children between the ages of 8-13 who are scheduled to receive any outpatient surgery (i.e. tonsillectomy, herniorrhaphy)
Not Eligible

You will not qualify if you...

  • Children with chronic illnesses (e.g., cancer)
  • Children with known neurodevelopmental disorders
  • Children on psychotropic medications prior to randomization

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

McMaster Children's Hospital

Hamilton, Ontario, Canada, L8S 4K1

Actively Recruiting

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Research Team

T

Toni Tidy, BHSc, CCRA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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