Learning from loss: study seeks to improve tough talks in pediatric cancer
NCT ID NCT07663539
First seen Jun 27, 2026 · Last updated Jul 29, 2026 · Updated 4 times
Summary
This study interviews bereaved parents and oncologists to understand how they discussed uncertainty during a child's cancer treatment. The goal is to find better ways for doctors and families to communicate about what the future may hold. Participants include parents whose child died 6 to 24 months ago and the doctors who cared for them.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could point toward better ways for doctors to discuss uncertain outcomes with families of children with cancer.
- What could go wrong
- This is a small, single-site interview study, so findings may not apply to other hospitals or cultures. It explores experiences, not a treatment.
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.
- Participants
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About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2026
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- 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.
Who is studied
Parents who have lost a child to cancer and the doctors who treated them.
- Ages
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18 years and older
- Sex
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Anyone
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: * All participants must be ≥ 18 years of age or legally emancipated * Parent Participants must have a child who: * Received cancer care from a clinician at St. Jude, as documented in the electronic medical record, AND * Died at least 6 months prior to enrollment, but no more than 24 months prior to enrollment. * Oncologist participants at St. Jude must: * Be listed as the primary oncologist as documented in the electronic medical record, AND * Have the respective patient's parent agreement to participate in the study. Exclusion Criteria: * Declining, refusal, or unwillingness to participate * Inability or unwillingness of research participant to give informed consent.
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Genom att skicka in godkänner du våra Användarvillkor
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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The study's own enquiry address
This study publishes an address for enquiries. See it below .
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Show contact details
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Genom att skicka in godkänner du våra Användarvillkor
Study contacts
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Contact
Email: •••••@•••••
Locations
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St. Jude Children's Research Hospital
RECRUITINGMemphis, Tennessee, 38105, United States
Contact Email: •••••@•••••
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