Patient-Generated Health Data Collection During Chemoradiotherapy for Lung Cancer

Part of paid clinical trials in New York, New York.

Sponsor
The New York Proton Center
Study ID
NCT06342284
Status
Recruiting

Conditions

  • Thoracic Cancer

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Proton Beam Radiation with or without concurrent chemotherapy — RADIATION
    Curative-intent fractionated proton beam thoracic radiotherapy, with or without concurrent chemotherapy

Study Details

This is an observational study involving the collection of patient-generated health data using an Apple Watch, a home pulse oximeter, and a smartphone during a course of proton beam radiotherapy for lung cancer. The study period over which this information is collected will range from the day of study enrollment until two weeks after radiotherapy completion. Subjects will complete a short satisfaction survey at the end of the study period. Other information that is collected as part of routine care for this patient population will be extracted from subjects' medical records during the study period and afterwards.

Key Dates

Start date
Mar 22, 2024
Status verified
Apr 2026
Primary completion
Mar 31, 2028
Completion
Mar 21, 2031

Study Design

Enrollment
40 participants (estimated)

Primary Outcome Measure

Demonstrate the feasibility of patient-generated health data collection during thoracic proton beam radiotherapy for lung cancer, based on the quantity of data collected from the day of radiotherapy initiation to the day of radiotherapy completion. [ Time Frame: 4-5 Weeks ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
New York Proton CenterNew YorkNew York10035
Ryan Holder, BS
646-968-9055
Thomas Mistretta, MS
646-568-5675
Nitin Ohri, MD (PRINCIPAL_INVESTIGATOR)
Charles Simone, MD (SUB_INVESTIGATOR)
Annemarie Shepherd, MD (SUB_INVESTIGATOR)
Stanislav Lazarev, MD (SUB_INVESTIGATOR)
Alexandra Hanlon, PhD (SUB_INVESTIGATOR)

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