New tool helps kids with cancer speak up about symptoms
NCT ID NCT04614662
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tested whether having children with cancer report their symptoms three times a week using a web-based tool (SPARK) could improve their quality of life. The tool alerted healthcare providers and linked to care pathways for managing symptoms. A total of 445 children aged 8–18 from 20 hospitals took part. The goal was to reduce symptom burden and fatigue.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Symptom screening and care pathway tool (SPARK)
- What this could lead to
- If it works, this approach could help children with cancer feel better during treatment by catching and managing symptoms early.
- What could go wrong
- This is a completed trial, so results are available but may not show a big improvement. The tool only helps with symptoms, not the cancer itself.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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445 people
The number who actually took part.
- Started
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Aug 2021
- Finished
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Oct 2023
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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8 to 18 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 8-18 years of age at enrollment * English or Spanish-speaking * Any newly diagnosed cancer * Have a plan for any chemotherapy, radiotherapy or surgery * Enroll within 28 days after treatment initiation Exclusion Criteria: * Cognitive disability (attending minimum second grade or equivalent) * Visual impairment (cannot see SPARK even with corrective lens)
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Get notified about this study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Children's Hospital
New Orleans, Louisiana, 70118, United States
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Children's Hospital Los Angeles
Los Angeles, California, 90027-6062, United States
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Connecticut Children's Medical Center
Hartford, Connecticut, 06106, United States
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Driscoll Children's Hospital
Corpus Christi, Texas, 78411, United States
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Kapi'olani Medical Center for Women & Children
Honolulu, Hawaii, 96826, United States
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Nemours Children's Health, Jacksonville
Jacksonville, Florida, 32207, United States
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Nemours Children's Hospital, Delaware
Wilmington, Delaware, 19803, United States
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Nemours Children's Hospital, Florida
Orlando, Florida, 32827, United States
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Phoenix Children's Hospital
Phoenix, Arizona, 85016-7710, United States
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Roswell Park Comprehensive Cancer Center
Buffalo, New York, 14203, United States
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The Hospital for Sick Children
Toronto, Ontario, M5G 1X8, Canada
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The Leland Stanford Junior University
Redwood City, California, 94305-2004, United States
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The Trustees of Columbia University in the City of New York
New York, New York, 10032, United States
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The University of Iowa
Iowa City, Iowa, 52242, United States
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The University of Texas Health Science Center at San Antonio
San Antonio, Texas, 78229-3901, United States
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The University of Texas M. D. Anderson Cancer Center
Houston, Texas, 77030, United States
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Unity Point Health - Blank Children's Hospital
Des Moines, Iowa, 50309, United States
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University of Colorado Denver
Aurora, Colorado, 80045-2571, United States
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Vanderbilt University Medical Center
Nashville, Tennessee, 37203-1161, United States
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Virginia Commonwealth University
Richmond, Virginia, 23298-0568, United States
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Washington University School of Medicine
St Louis, Missouri, 63110, United States
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Other studies related to the condition(s) this trial covers.
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