Actively Recruiting

Age: 0Years - 18Years
All Genders
ID07060326

Digital Literacy in Caregivers of Pediatric Surgery Patients

Led by Brittany Willer · Updated on 2025-07-11

300

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to describe the digital literacy levels among caregivers of children undergoing surgery. The study focuses on caregivers of pediatric surgical patients and explores how factors like minority race, non-English primary language, and living in areas with limited resources may affect digital literacy. Participants in this observational study are caregivers of pediatric patients under 18 years old presenting for surgery. Caregivers will complete surveys using a questionnaire delivered via REDCap during the perioperative period to assess their digital literacy and health literacy. Participants will be involved from enrollment through the perioperative time. Researchers will measure digital literacy using the EDLQ digital literacy scores and health literacy using the eHEALS Health Literacy scores. The study will monitor these outcomes throughout the study period ending around July 2028.

CONDITIONS

Brief Title

Digital Literacy in Caregivers of Pediatric Surgery Patients

Who Can Participate

Age: 0Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Caregivers of children under 18 years presenting for surgery at NCH
  • Primary language must be English, Spanish, Arabi, Nepali, or Somali
Not Eligible

You will not qualify if you...

  • Patients who are 18 years of age or older
  • Wards of the state
  • Patients who are missing address information

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote)

Surveillance

Duration - From enrollment to end of perioperative time

Participants complete surveys to assess digital literacy during the perioperative period.

1 survey during the perioperative period

Trial Site Locations

Total: 1 location

1

Nationwide Children's Hospital

Columbus, Ohio, United States, 43205

Actively Recruiting

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Research Team

C

Catherine Roth, MPH

J

Julie Rice-Weimer, RN

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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