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Evaluating an eHealth Solution for Screening in Pediatric Care

NCT04506294 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 320

Last updated 2024-06-26

Study results available
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Summary

This study will evaluate the predictive validity of a game-based screening system based on child self-report measures.

The core study hypotheses are that (1) in-game assessments will predict problematic recovery (child pain and posttraumatic stress symptoms \[PTSS\]) and (2) parents in the intervention group will report greater confidence in managing child recovery.

Conditions

  • Pain
  • Stress Disorders, Post-Traumatic

Interventions

BEHAVIORAL

eScreen system

The eScreen system is composed of a child screening component and a parent information component. The child screening component is delivered via a game-like interface and includes assessment of current pain, PTSS, and functional recovery. Children are asked to play the game at least 3x/week. The parent information component consists of text / email messages sent to parents at least weekly that summarize child ratings and include a link to an online dashboard with additional personalized information for parents.

Sponsors & Collaborators

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

    collaborator NIH

  • University of Kentucky

    collaborator OTHER

  • Radiant Creative Group, LLC

    collaborator INDUSTRY

  • Children's Hospital of Philadelphia

    lead OTHER

Principal Investigators

  • Nancy Kassam-Adams, PhD · Center for Injury Research & Prevention, Children's Hospital of Philadelphia

Study Design

Allocation
RANDOMIZED
Purpose
SCREENING
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
8 Years
Max Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-03-17
Primary Completion
2022-07-21
Completion
2022-07-21

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04506294 on ClinicalTrials.gov