Understanding recovery in children after cancer surgery
Official title: Digital Biomarker and Omics-Based Assessment of Surgical Resiliency in Children Undergoing Solid Tumor Resection: A Pilot Feasibility Study
Run by Mayo Clinic · NCT06674811 · Data updated 2026-11-12
This study looks at how children aged 3-18 and their families recover after cancer surgery by using smartwatches and surveys to gather information over a year.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 3 Years to 25 Years |
| Sex | All |
| Enrollment | 40 (estimated) |
| Sponsor | Mayo Clinic Academic / other |
| Locations | 1 site (Rochester, Minnesota) |
| Status | Recruiting |
| Started | January 15, 2025 |
| Main results expected | January 31, 2030 |
| Study ends | January 31, 2030 |
| Registry record updated | September 14, 2026 |
| Trial ID | NCT06674811 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include children aged 3-18 with solid tumors such as neuroblastoma, sarcoma, or kidney tumors, along with their primary caregivers.
✕Probably not a fit
Patients who are pregnant or prisoners will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to explore how children and their families recover from major cancer surgeries by utilizing smartwatches and questionnaires. Participants, including pediatric patients aged 3-18 and their primary caregivers, will wear smartwatches to collect digital biomarkers and complete surveys about their recovery. Additionally, blood samples will be taken during routine clinical blood draws to analyze proteins and metabolites associated with stress post-surgery. The study will track recovery patterns for up to one year following surgery.
Why it matters
Potential benefit: If successful, this study could lead to improved strategies for enhancing recovery and resilience in children undergoing cancer surgery.
How similar studies have gone: While the use of digital biomarkers in recovery monitoring is emerging, this specific approach is novel and has not been extensively tested in similar studies.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 3-25 years old at enrollment * With solid tumors of the chest, abdomen, and extremities including neuroblastic tumors, sarcoma including soft tissue and bone, kidney tumors, liver tumors, ovarian tumors, lung and pleural-based tumors, and intestinal tumors -OR- * Guardian or primary caregiver of patient 3-25 years old with one of the aforementioned tumors. Exclusion Criteria: * Patients who are known to be pregnant or prisoners.
Where it's running
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Mayo Clinic
Rochester, Minnesota, United States Recruiting
Study contacts
- Principal investigator: Stephanie Polites, M.D., M.P.H. — Mayo Clinic
- Study coordinator: Mayo Clinic Pediatric Surgery Clinical Research Unit
- Email: DOSCRO2@mayo.edu
- Phone: 507-266-4467
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.