Actively Recruiting

Phase Not Applicable
Age: 5Years - 10Years
All Genders
ID06324955

A Prospective Randomized Study Comparing Positive Language versus Common Language During Inhalational Induction of Anesthesia in Children

Led by Boston Children's Hospital · Updated on 2026-01-09

128

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to compare how the use of common (standard of care) language versus positive language by clinicians during the inhalational induction of anesthesia affects anxiety and negative behaviors in children aged 5 to 10 years. The study focuses on measuring the impact of these different communication styles during anesthesia induction in a randomized, parallel group design. Participants will be randomly assigned to one of two groups: one where the anesthesiologist uses scripted common or standard language during induction, and another where scripted positive language is used. This behavioral intervention is applied during the inhalational anesthesia induction process. Children involved in the study will be monitored during anesthesia induction for compliance with the procedure, length of induction, and any verbal refusal to wear the anesthesia mask. The primary outcome is induction compliance, assessed during the approximately one-day study period. Secondary outcomes include the length of induction and verbal refusal of the mask. The study is sponsored by Boston Children's Hospital and does not involve masking or blinding.

CONDITIONS

Brief Title

Language During Inhalational Induction

Who Can Participate

Age: 5Years - 10Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthy patients classified as ASA 1 or 2
  • Non-emergency surgical cases
  • Children aged 5 to 10 years
  • Patients receiving inhalational induction of anesthesia
Not Eligible

You will not qualify if you...

  • Non-English speaking patients
  • History of prior inhalational anesthesia inductions
  • Hearing difficulties
  • Behavioral difficulties such as autism or oppositional defiant disorder
  • Patients receiving premedication other than midazolam before anesthesia induction

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Inhalational Induction

Duration - About 1 day

Participants receive inhalational anesthesia induction with either positive or common/standard scripted language used by the anesthesiologist during the procedure.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

Boston Children's Hospital

Boston, Massachusetts, United States, 02115

Actively Recruiting

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Research Team

J

John Fiadjoe, MD

R

Rachel Bernier, MPH

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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