Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06722378

A Trial to Improve Family Clinical Note Access and Outcomes for Hospitalized Children

Led by University of Wisconsin, Madison · Updated on 2025-12-18

630

Participants Needed

3

Research Sites

208 weeks

Total Duration

On this page

Sponsors

U

University of Wisconsin, Madison

Lead Sponsor

A

Agency for Healthcare Research and Quality (AHRQ)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study will test if giving parents access to their child's medical notes on a bedside tablet: * helps them get more involved in their care * helps identify safety concerns Parents of hospitalized children will be randomly assigned to either use the Bedside Notes tool or follow usual care. To see if this approach improves care and safety, researchers will measure: * note access * parent-reported safety concerns * overall experiences

CONDITIONS

Official Title

A Trial to Improve Family Clinical Note Access and Outcomes for Hospitalized Children

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Parents or guardians who speak English or Spanish
  • Parents or guardians of children under 12 years old hospitalized on a general pediatric service at one of the 3 centers
  • Age 18 years or older
Not Eligible

You will not qualify if you...

  • Parents of children 12 years of age or older
  • Parents unable to give written informed consent
  • Parents of children admitted for suspected abuse or neglect
  • Children expected to be discharged within 24 hours

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

Children's Hospital of Los Angeles

Los Angeles, California, United States, 90027

Actively Recruiting

2

Seattle Children's Hospital

Seattle, Washington, United States, 98105

Not Yet Recruiting

3

American Family Children's Hospital

Madison, Wisconsin, United States, 53792

Actively Recruiting

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Research Team

M

Michelle Kelly, MD, PhD

CONTACT

A

Amanda Gatewood

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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