Recruiting

MyCap

Sponsor:

Ohio State University Comprehensive Cancer Center

Code:

NCT07619391

Conditions

Pancreatic Adenocarcinoma

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Electronic Health Record Review

Smartphone Application-based Intervention

Survey Administration

Study Details

Brief summary:

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.

Conditions

Pancreatic Adenocarcinoma

Study ID

NCT07619391

Start date

Mar 10, 2026

Status verified date

May, 2026

Completion date

Dec 31, 2027

Anticipated

Primary completion date

Dec 31, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

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

Study Design

Enrollment

30 participants

Anticipated

Intervention Model

Single group

Primary purpose

Health Services Research

Interventions and Outcome Measures

Arms

experimental: Health Services Research (MyCap app)

Patients download the MyCap app onto their phone and fill out a daily time log in the app for 8 weeks.

Interventions

Electronic Health Record Review

Ancillary studies

Smartphone Application-based Intervention

Receive access to MyCap application

Survey Administration

Ancillary studies

Primary outcome measure

  • Retention rate (feasibility) [ Time Frame: Up to 8 weeks ]
  • Adherence rate (feasibility) [ Time Frame: Up to 8 weeks ]
  • System usability survey (feasibility) [ Time Frame: Up to 8 weeks ]

Central Contacts and Locations

Central contacts

The Ohio State University Comprehensive Cancer Center

800-293-5066OSUCCCClinicaltrials@osumc.edu

Locations

Ohio State University Comprehensive Cancer Center

Recruiting

Columbus, Ohio, United States, 43210

Contacts

Pamela W. Lu, MD

614-293-7171Pamela.lu@osumc.edu

Principal Investigator:

Pamela W. Lu, MD

More Information

Sponsor

Ohio State University Comprehensive Cancer Center

Last update posted

Jun 2, 2026

Last verified

May, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Ohio State University Comprehensive Cancer Center on 2026-06-02.