Shareholder-driven Co-design and Piloting of Spanish Educational Videos About High Yield Pediatric Oncology Topics

February 12, 2026 updated by: University of Colorado, Denver
Families of children with cancer who speak languages other than English experience inequalities in healthcare, but little research has been done on solutions to improve care for these families. This study will partner parents with medical interpreters and clinicians to create educational videos about key cancer topics in Spanish and test their use as a tool to improve caregiver knowledge and experience in the setting of a language barrier. The project will lead to a future career development award application that increases the number of available languages and studies how multilingual educational videos impact caregiver knowledge and experience

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Estimated)

10

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Colorado
      • Aurora, Colorado, United States, 80045
        • Recruiting
        • Children's Hospital Colorado
        • Contact:
        • Principal Investigator:
          • Melanie Stall, MD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

Aims 1 and 2 (Video Development Phase):

  • Legal caregiver aged ≥18 years of a child/young adult (0-25 years) undergoing active cancer treatment in low-intensity phases or off therapy.
  • Native or fluent Spanish speaker.
  • Willing and able to provide verbal consent.
  • Willing to comply with study procedures and be available for the study duration.

Aim 3 (Video Pilot Phase):

  • Legal caregiver aged ≥18 years of a child/young adult (0-25 years) with newly diagnosed or relapsed/refractory cancer (≤1 month).N
  • Native or fluent Spanish speaker.
  • Requires an interpreter for medical conversations.
  • Willing and able to provide verbal consent.
  • Willing to comply with study procedures and be available for the study duration.

Exclusion Criteria:

Aims 1 and 2:

  • Insufficient cognitive functioning to complete study procedures (as determined by PI).
  • Caregiver of a child/young adult who did not receive cancer-directed therapy.
  • Caregiver of a child/young adult receiving high-intensity cancer treatment.
  • Unable to read and speak Spanish fluently.

Aim 3:

  • Insufficient cognitive functioning to complete study measures (as determined by PI).Caregiver of a child/young adult who did not receive cancer-directed therapy.
  • Caregiver of a child/young adult not receiving cancer-directed therapy.
  • Diagnosis of new or relapsed/refractory cancer occurred >1 month prior to enrollment.
  • Unable to speak Spanish fluently.
  • Does not require an interpreter for medical conversations.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Pilot educational videos
Pilot education videos with Spanish-speaking parents as a tool to improve caregiver knowledge, satisfaction, confidence in caring for their child, and level of overwhelm.
Spanish-language video to impart knowledge and understanding to parents caring for children with cancer

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Feasibility of Implementing a Spanish-Language Educational Video Intervention
Time Frame: 6 months
The feasibility of implementing a Spanish-language educational video intervention will be assessed using the Feasibility of Intervention measure.
6 months
Acceptability of Implementing a Spanish-Language Educational Video Intervention
Time Frame: 6 months
The acceptability of the Spanish-language educational video intervention will be assessed using the Acceptability of Intervention Measure.
6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Impact on caregiver knowledge measured by post-intervention surveys
Time Frame: 12 months
The impact of the intervention on caregivers knowledge will be assessed through post-intervention questionnaires measuring changes in knowledge about caregiving, satisfaction with the educational material, and confidence in caring for their child.
12 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 2, 2025

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 1, 2027

Study Registration Dates

First Submitted

January 22, 2025

First Submitted That Met QC Criteria

December 3, 2025

First Posted (Actual)

December 17, 2025

Study Record Updates

Last Update Posted (Actual)

February 13, 2026

Last Update Submitted That Met QC Criteria

February 12, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 25-0595.cc
  • NCI-2025-08026 (Other Identifier: Clinical Trials Reporting Program)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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