๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-05-27

MyCap Mobile Application for Tracking Time Burden of Treatment for Patients With Pancreatic Cancer (NCT07619391)

A Mobile App for Tracking Time Burden of Pancreatic Cancer Treatment: A Single-Arm Feasibility Study

๐ŸŸข Recruiting Observational / Diagnostic ๐Ÿง  Behavioral & Psychological Program Sponsor: Ohio State University Comprehensive Cancer Center

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

This clinical trial tests the feasibility of using the MyCap mobile application (app) for tracking time burden from treatment for patients with pancreatic cancer. Pancreatic cancer is best treated with many care teams, such as medical oncology and surgery, requiring patients to dedicate significant time coordinating appointments among different doctors. This time commitment is referred to as time toxicity, defined as the time spent undergoing cancer-related medical care, such as emergency visits, ambulatory care, lab and infusion visits, hospitalizations, and the commuting and waiting times associated with each. At present, time toxicity is still understudied within the medical literature, with no gold standard established for the method of measurement. The MyCap mobile app may be a feasible way to track the time burden from treatment for patients with pancreatic cancer.

Who can join: Review the eligibility criteria below.

Location: Ohio State University Comprehensive Cancer Center โ€” Columbus, Ohio

Age range: 18 Years

๐Ÿงช Interventions in This Study

  • Electronic Health Record Review (OTHER)
  • Smartphone Application-based Intervention (BEHAVIORAL)
  • Survey Administration (OTHER)

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)

  • Ohio State University Comprehensive Cancer Center โ€” Columbus, Ohio

๐Ÿ“ž Contact the Study Coordinator

Phone: (800) 293-5066

Email: OSUCCCClinicaltrials@osumc.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.

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†—