Testing the Reliability and Validity of the CIBA

Completed

Conditions studied: Quality Improvement

In brief

The overall objective of the study is to improve the experience for pediatric patients undergoing anesthesia inductions. The specific objective for this proposal is to establish whether the CIBA tool demonstrates inter-rater reliability and concurrent validity with the Induction Compliance Checklist.

Key facts

Study ID

NCT02882594

Run by

Children's Hospital Medical Center, Cincinnati

People needed

384

Starts

2016-03-01

Expected to finish

2017-06-01

Last updated by the study team

2017-08-01

Who can join

Age: 1 and older, up to 13. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Presenting to Same Day Surgery department at CCHMC base campus for any surgical or Intervention Radiology procedure
• Ages 1-13 years old
• Male or female
• Patients of any ethnicity
• Family and participant communicate primarily in English
• Patients with normal neurocognitive development
• Patients undergoing inhalation induction using an anesthesia mask
• American Society of Anesthesiologists (ASA) physical classification status I, II, or III
• Patients who do or do not receive a premedication for anxiety
• Parent/guardian present at the induction of anesthesia

You may not qualify if…

• Guardian unavailable to give consent
• Neurocognitive delays
• Tracheostomy
• Intravenous (IV) induction or nitrous sedation prior to IV induction
• Coordinators unable to observe or fully observe the induction
• CIBA assessment not completed by anesthesia provider

Where it is running

• Cincinnati Children's Medical Center — Cincinnati, Ohio, United States

Full record on ClinicalTrials.gov

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