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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorOhio State University Comprehensive Cancer Center

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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)

Disqualifiers

Prisoners

Patients undergoing cancer surveillance

Trial design

Design model

Single group

Treatments tested in this trial

  • Electronic Health Record Review

    Other intervention

    Ancillary studies

  • Smartphone Application-based Intervention

    Behavioral

    Receive access to MyCap application

  • Survey Administration

    Other intervention

    Ancillary studies

Treatment groups

30 Participants
are divided into 1 treatment group
Group A: Health Services Research (MyCap app)Experimental treatment 3 interventions

Trial outcomes

Primary outcomes

1

Retention rate (feasibility)

Defined as the number of participants who enroll in the study and complete at least one time log during the study period.

Time frame
Up to 8 weeks
2

Adherence rate (feasibility)

Adherence is defined as the percentage of patients who completed over 80% of time logs. Given that this study is evaluating a daily time log over 8 weeks, adherence would require participants to fill out at least 44-time logs.

Time frame
Up to 8 weeks
3

System usability survey (feasibility)

Time frame
Up to 8 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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