Actively Recruiting
Wearable Activity Tracking to Curb Hospitalizations
Led by University of California, San Francisco · Updated on 2026-04-17
260
Participants Needed
1
Research Sites
142 weeks
Total Duration
On this page
Sponsors
U
University of California, San Francisco
Lead Sponsor
N
National Cancer Institute (NCI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study is being done to collect patient generated health data to predict the risk of patients needing emergency department visits or hospitalization before, during. and after receiving radiation therapy.
CONDITIONS
Official Title
Wearable Activity Tracking to Curb Hospitalizations
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age >= 18.
- Eastern Cooperative Oncology Group (ECOG) performance status =< 2.
- Able to understand study procedures and to comply with them for the entire length of the study.
- Ability of individual or legal guardian/representative to understand a written informed consent document, and the willingness to sign it.
- Diagnosis of invasive malignancy.
- Able to ambulate independently (without the assistance of a cane or walker).
- Planned treatment with fractionated external beam radiotherapy over at least 5 days (no fractional requirement).
- Not a previous participant on this protocol for subsequent courses.
You will not qualify if you...
- Participants bound to a wheelchair.
- Participants unable to ambulate independently (needing assistance of cane or walker).
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of California, San Francisco
San Francisco, California, United States, 94143
Actively Recruiting
Research Team
I
Imani Dunn
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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