Childhood cancer survivor remote health study pulled before start
NCT ID NCT07222358
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aimed to see if adult survivors of childhood cancer could use wearable devices, surveys, and lab tests at home to monitor their heart health. It was designed for survivors who had certain cancer treatments. However, the study was withdrawn before enrolling any participants, so no results are available.
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Study facts
What this study's own registry entry says, in plain language.
- Expected to start
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Apr 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2027
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
All participants who meet eligibility criteria and consent to enrollment on the study.
- Ages
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18 years and older
- 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: * Participant is ≥18 years of age * Participant is enrolled in the St. Jude Life (SJLIFE) cohort * Participant is able and willing to provide informed consent * Participant has signed a separate consent for the St. Jude banking protocol (TBANK) * Participant received anthracycline (≥100 mg/m²), chest or abdominal radiation as part of childhood cancer treatment * Participant owns a SmartPhone compatible with the vendor platform, Apple HealthKit, and Dexcom (a wearable device that continuously tracks glucose levels) * Participant verbalizes understanding directions for completing remote study activities with the third-party partner * Participant is fluent in English Exclusion Criteria: * Participant uses a continuous glucose monitor for diabetes management or has diabetes requiring insulin or more than 1 agent for treatment at baseline * Participant is currently enrolled on an intervention or active longitudinal monitoring ancillary 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.
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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