e-Health Psychosocial Stress and Symptom Management (ePSMI) for Pancreatic Cancer Patients (NCT06893276) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
e-Health Psychosocial Stress and Symptom Management (ePSMI) for Pancreatic Cancer Patients
United States60 participantsStarted 2026-08-01
Plain-language summary
The purpose of this research is to evaluate a new, web-based program among patients with pancreatic cancer aimed at reducing psychosocial stress.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
. Greater than 18 years of age.
. Spanish or English speaker with ability to read one of these languages.
. Diagnosis of pancreatic cancer.
. Patients diagnosed with pancreatic neuroendocrine tumor (PNET).
Exclusion criteria
. Patients unable to read Spanish or English, as participants will not be unable to complete surveys.
. Have a history of severe psychiatric illness (e.g., psychosis, active suicidality, inpatient treatment in the past 12 months).
. Have any condition that, in the opinion of the investigator, would compromise the well-being of the patient or the study or prevent the patient from meeting or performing study requirements.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Percentage of Participants Recruited
Timeframe: Up to 1 year.
2
Percentage of Participants Retained
Timeframe: Up to 1 year.
3
Percentage of Study Participation
Timeframe: Up to 1 year.
4
Number of Calls
Timeframe: Up to 10 weeks.
5
Theoretical Framework on Acceptability Questionnaire
Timeframe: Up to 10 weeks.
6
Functional Assessment of Cancer Therapy (FACT) - Functional Hepatobiliary-Pancreatic Symptom Index (FHSI)-18
Timeframe: Up to 10 weeks.
7
Patient-Reported Outcomes Measurement Information System - Pain Short Form