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Symptom Trajectory Approaches to Research

Defining Symptom Trajectories to Inform Risk-Stratified Approaches to Symptom Management in Children With Advanced Cancer

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07804875
Acronym
STAR
Enrollment
228
Registered
2026-09-04
Start date
2026-12-01
Completion date
2031-05-31
Last updated
2026-09-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Advanced Cancer, Cancer Treatment, Metastatic Disease, Progressive Disease, Recurrent Cancer

Keywords

Undergoing cancer treatment, undergoing cancer comfort care

Brief summary

The goal of this observational study is to understand how cancer makes children feel over time. The main things the researchers hope to learn are: * When and how often do children have different feelings or sickness; * Why do these feelings happen; and, * How these feelings change a child's overall health. Participants will answer simple surveys about their health.

Detailed description

The use of conventional and novel therapeutics to treat children with advanced cancer leads to burdensome physical and psychological symptoms. Advanced cancer is metastatic upon initial diagnosis, relapsed, progressed, or refractory to treatment, resulting in an uncertain and prolonged disease course. Symptom burden and associated suffering are amplified for these children due to disease burden, intense therapy, and often lengthy treatment. Symptom patterns (trajectories) have been identified in children diagnosed with early-stage cancer, but research characterizing symptom patterns over time in the understudied patient population of children with advanced cancer is sparse.

Interventions

Participants will complete several surveys about their quality of life and health.

Sponsors

University of Wisconsin, Madison
Lead SponsorOTHER
National Cancer Institute (NCI)
CollaboratorNIH
Nationwide Children's Hospital
CollaboratorOTHER
Oregon Health and Science University
CollaboratorOTHER
Children's Hospital Los Angeles
CollaboratorOTHER
New York Presbyterian Hospital
CollaboratorOTHER
OHSU Doernbecher Children's Hospital
CollaboratorOTHER
Columbia University
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
8 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

- Children: * Aged 8-18 years * Diagnosis of advanced cancer of any type made by the hematology, oncology, or cellular therapy team * Undergoing cancer treatment or comfort care * Be English or Spanish literate Inclusion Criteria - Caregivers: * Aged \>18 * Caregiver of a child diagnosed with advanced cancer * English or Spanish literate * Identified as being substantially involved in caring for the child

Exclusion criteria

* Any condition that would prevent participants from completing surveys

Design outcomes

Primary

MeasureTime frameDescription
Change in Pediatric Patient-Reported Outcome Common Terminology Criteria for Adverse Events (Ped-PRO-CTCAE)Baseline, bi-weekly for 4 monthsPed-PRO-CTCAE evaluates pediatric cancer symptoms using patient or caregiver reports scored on a 0-to-3 scale across attributes like frequency, severity, and interference. 38 items are scored 0-3, where 0 = never (or equivalent) and 3 = all the time (or equivalent). Scores range from 0 to 114, with higher scores indicating worse symptoms. This score will be used to measure the trajectory of symptoms over time.

Secondary

MeasureTime frameDescription
Change in PROMIS Pediatric Global Health 7Baseline, bi-weekly for 4 monthsPROMIS Pediatric Global Health 7 is a 7-item survey used to measure overall physical, mental, and social health in children and adolescents. It is scored using a 5-point Likert scale, where 1 = poor and 5 = excellent. Scores range from 7 to 35, with higher scores indicating better global health.
Change in PROMIS Pediatric Mobility - Short Form 7aBaseline, bi-weekly for 4 monthsPROMIS Pediatric Mobility is a 7-item questionnaire that evaluates self-perceived physical mobility and functioning in children and adolescents. It uses a 5-point Likert scale ranging from "Without no trouble" to "Not able to do". Raw scores range from 7 to 35. Raw scores are translated into normalized T-scores with a US population-level mean of 50 and a standard deviation (SD) of 10. A T-score of 50 represents average mobility for the general population. Scores above 50 mean better-than-average mobility, while scores below 50 indicate greater impairment.
Change in PROMIS Pediatric Physical Stress Experiences - Short Form 8aBaseline, bi-weekly for 4 monthsPROMIS Physical Stress Experiences is an 8-item questionnaire designed to measure physical symptoms of stress in children and adolescents. It is scored by summing the raw item responses (ranging from 8 to 40) and converting that total into a standardized T-score. The raw score maps to a standardized T-score with a mean of 50 and a standard deviation (SD) of 10 for the general population. Higher T-scores reflect a greater level of physical stress.

Countries

United States

Contacts

CONTACTSabrina Cordon-Royer
cordonroyer@wisc.edu
PRINCIPAL_INVESTIGATORKathleen (Kitty) Montgomery, PhD, RN, PCNS-BC

University of Wisconsin, Madison

PRINCIPAL_INVESTIGATORKristine Kwekkeboom, PhD, RN, FAAN

University of Wisconsin, Madison

PRINCIPAL_INVESTIGATORRoger Brown, PhD

University of Wisconsin, Madison

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 5, 2026