Video Inspired Discussions About Ethical Outcomes in Pediatrics

NCT06786104 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 567

Last updated 2026-05-14

No results posted yet for this study

Summary

The goal of this clinical trial is to learn if the VIDEO-PEDS intervention works to improve Goals of Care communication between clinicians and parents of children with cancer.

The main questions it aims to answer are:

Does the intervention improve Goals of Care documentation? Does it improve patient outcomes (including less invasive preferences for resuscitation and interventions, less hospital utilization, and more palliative care and hospice use)? Does it improve parent outcomes (including health satisfaction and feeling heard and understood per survey scores)?

Conditions

  • Pediatric Cancer

Interventions

OTHER

VIDEO-PEDS

Following enrollment, parents will receive a link to view the refined video decision aid that is designed to prompt parents to think about their goals of care for their child with cancer, and then to react by engaging in communication with a trained member of the research team called the Navigator and eventually their clinical team over the course of the 9-month study duration.

OTHER

VIDEO-PEDS pilot

This is the 3-month pilot version of the intervention, which will be further developed for the eventual RWCT.

OTHER

Focus Group

Parents will view the Video aid and provide fascilitated feedback in an audio-recorded virtual group setting.

Sponsors & Collaborators

  • National Cancer Institute (NCI)

    collaborator NIH
  • Dartmouth-Hitchcock Medical Center

    collaborator OTHER
  • Dana-Farber Cancer Institute

    collaborator OTHER
  • Yale University

    collaborator OTHER
  • Emory University

    collaborator OTHER
  • Children's Healthcare of Atlanta

    collaborator OTHER
  • University of Alabama at Birmingham

    collaborator OTHER
  • Massachusetts General Hospital

    lead OTHER

Principal Investigators

  • Angelo Volandes, MD · Dartmouth-Hitchcock Medical Center

Study Design

Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-05-05
Primary Completion
2030-01-15
Completion
2030-04-15

Countries

  • United States

Study Locations

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Entities

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 NCT06786104 on ClinicalTrials.gov