MyCap app to track time burden of pancreatic cancer treatment
Official title: A Mobile App for Tracking Time Burden of Pancreatic Cancer Treatment: A Single-Arm Feasibility Study
Run by Ohio State University Comprehensive Cancer Center · NCT07619391 · Data updated 2026-11-12
This study tests whether a mobile app can help adults with pancreatic cancer log the time they spend on cancer care.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 30 (estimated) |
| Sponsor | Ohio State University Comprehensive Cancer Center Academic / other |
| Locations | 1 site (Columbus, Ohio) |
| Status | Recruiting |
| Started | March 10, 2026 |
| Main results expected | December 31, 2027 |
| Study ends | December 31, 2027 |
| Registry record updated | June 2, 2026 |
| Trial ID | NCT07619391 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18 years or older with pancreatic adenocarcinoma who are either undergoing active treatment or about to start treatment within 30 days, English-speaking, and owning a smartphone.
✕Probably not a fit
Patients without smartphone access, non-English speakers, or those not receiving active treatment may not benefit from this approach.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The trial explores feasibility of using the MyCap smartphone application for patients with pancreatic adenocarcinoma to self-track time spent on treatment-related care over an 8-week period. Participants record daily time logs and may have their electronic health records reviewed and complete surveys as part of the intervention. The study will determine if the app is practical and acceptable for measuring time toxicity in this population. Recruitment is limited to adults with active treatment plans, English speakers, and smartphone access, at a single center in Columbus, Ohio.
Why it matters
Potential benefit: If successful, the app could provide a practical way to quantify and manage the time patients spend on treatment.
How similar studies have gone: Time-tracking and patient-reported burden methods have shown feasibility in other cancer types, supporting potential utility for pancreatic cancer.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adults ≥ 18 years old * Diagnosed with pancreatic adenocarcinoma undergoing active treatment or planning to start active treatment within the next 30 days * English speaking * Access to a smartphone (Android or iOS) Exclusion Criteria: * Prisoners * Patients undergoing cancer surveillance
Where it's running
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Ohio State University Comprehensive Cancer Center
Columbus, Ohio, United States Recruiting
Study contacts
- Principal investigator: Pamela W Lu, MD — Ohio State University Comprehensive Cancer Center
- Study coordinator: The Ohio State University Comprehensive Cancer Center
- Email: OSUCCCClinicaltrials@osumc.edu
- Phone: 800-293-5066
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.