๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-04-06

Patient-Generated Health Data Collection During Chemoradiotherapy for Lung Cancer (NCT06342284)

Patient-Generated Health Data Collection During Chemoradiotherapy for Lung Cancer: A Pilot Study

๐ŸŸข Recruiting Interventional Protocol ๐Ÿ“Š Observational Clinical Research Sponsor: The New York Proton Center

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

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.

Who can join: Review the eligibility criteria below.

Location: New York Proton Center โ€” New York, New York

Age range: 18 Years

๐Ÿงช Interventions in This Study

  • Proton Beam Radiation with or without concurrent chemotherapy (RADIATION)

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (1 Sites)

  • New York Proton Center โ€” New York, New York

๐Ÿ“ž Contact the Study Coordinator

Phone: (718) 405-8550

Email: nitin.ohri@einsteinmed.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Thoracic Cancer clinical trials

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—