Incorporating Biometric Data for Patients Receiving Concurrent Chemotherapy & RT

Part of paid clinical trials in Wilmington, North Carolina.

Sponsor
UNC Lineberger Comprehensive Cancer Center
Study ID
NCT05937659
Status
Not Yet Recruiting

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Conditions

  • Cancer

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Accepted

Study Details

This study will assess the feasibility of incorporating biometric data via wearable health technology (WHT) into the radiation oncology (RO) clinic workflow for patients receiving concurrent radiation therapy and systemic therapy (CRT) for cancer. The investigators hypothesize that a practical workflow could be created within a busy community RO practice that will allow providers and patients to readily appreciate physiologic declines during concurrent CRT. Subjects will be asked to wear a device as part of this study that will collect their biometric data (heart rate, number of steps taken per day, etc) called a WHT device throughout their treatment and for 4 weeks afterward. Subjects will be asked to upload the data from their devices onto the computers in the clinic for the assessment.

Key Dates

Start date
May 15, 2026
Status verified
Apr 2026
Primary completion
Oct 30, 2027
Completion
Oct 30, 2027

Study Design

Enrollment
20 participants (estimated)

Arms

  • Arm: Biometric Data Collection
    Adult subjects with cancer and prescribed concurrent systemic therapy and radiation therapy and enrolled in the study.

Primary Outcome Measure

The rate of technology adoption [ Time Frame: Up to 12 weeks ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Novant Health Cancer Institute Radiation OncologyWilmingtonNorth Carolina28401
Bridgette Cline
910-667-7259
Lukasz Mazur (PRINCIPAL_INVESTIGATOR)

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