- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07288476
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
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
- Name: Melanie Stall, MD
- Phone Number: 720-777-1234
- Email: melanie.stall@childrenscolorado.org
Study Locations
-
-
Colorado
-
Aurora, Colorado, United States, 80045
- Recruiting
- Children's Hospital Colorado
-
Contact:
- Glenn Buck
- Phone Number: 720-777-3442
- Email: glenn.buck@childrenscolorado.org
-
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.
Sponsor
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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