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Improving Treatment-Related Symptom Management in Adolescents and Young Adults With Cancer

Improving Treatment-Related Symptom Management in Adolescents and Young Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04594096
Enrollment
20
Registered
2020-10-20
Start date
2021-09-30
Completion date
2023-12-31
Last updated
2024-05-09

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

Conditions

Cancer

Brief summary

This study will test the acceptability and feasibility of a telehealth intervention to improve communication between patients and medical providers in adolescent and young adult (AYA) cancer patients receiving chemotherapy treatment.

Interventions

Receiving telehealth visits with a medical provider (MD or NP) 2-3 days after last chemotherapy administration in the cycle

BEHAVIORALStandard of Care

Receiving care as usual from the UC Davis Comprehensive Cancer Center

Sponsors

University of California, Davis
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

2 telehealth visits with a medical provider (either an MD or NP) after last chemotherapy administration in the cycle, or as otherwise indicated

Eligibility

Sex/Gender
ALL
Age
12 Years to 29 Years
Healthy volunteers
No

Inclusion criteria

* Patients with cancer undergoing active treatment and who have received at least two cycles of chemotherapy * Access to Epic MyChart (we will facilitate access to MyChart for interested patients who are not yet signed up) * Access to a smartphone or tablet to access EPIC MyChart telehealth appointments

Exclusion criteria

* Non-English or non-Spanish speaking patients * Potentially completing therapy during study period (including follow-up period) or plans to leave UCDCCC during study period

Design outcomes

Primary

MeasureTime frameDescription
Proportion of Patients Completing the Trialend of the study period (6 cycles of chemotherapy for each participant, where each cycle is 14-28 days)\>65% of enrolled patients will complete the trial

Secondary

MeasureTime frameDescription
Survey Response Rateend of the study period (6 cycles of chemotherapy for each participant, where each cycle is 14-28 days)\>%70% of enrolled patients will complete the survey instruments
Telemedicine Satisfaction and Usefulness Questionnaire (TSUQ)end of the study period (6 cycles of chemotherapy for each participant, where each cycle is 14-28 days)A composite score of ≥40 (based on 10 items with a Likert scale of 1-5 strongly disagree to strongly agree)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026