NCT07591480Not yet recruiting
Barriers And Facilitators To Clinical Trial Enrollment: A Qualitative Study Of Pancreatic Cancer Patients
Source: ClinicalTrials.gov · Last updated 15 May 2026
Brief summary (registry, in English)
The purpose of this research is to understand why some groups of people do not join clinical trials as much as others. These groups can include people from different racial or ethnic backgrounds, people with lower incomes, people who live in rural areas, and people who speak different languages. Investigators interview participants to learn about their experiences with clinical trials. By learning from them, investigators hope to find better ways to help more people learn about, join, and stay in clinical trials so that research is fair and helpful for everyone.
- Status (registry)
- Not yet recruiting
- Study type
- Observational
- Enrollment
- 20 (estimated)
- First submitted
- 8 Apr 2026
- Start date
- 1 May 2026
- Primary completion date
- 1 Oct 2026
- Lead sponsor
- M.D. Anderson Cancer Center
- Diseases
- Pancreatic cancer
- NCT number
- NCT07591480
What you commit to
- Study type: Observational
- Planned participants: 20
- From 1 May 2026 to the primary completion date, 1 Oct 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other
- An individual who meets any of the following criteria will be excluded from participation in this study:
- Patients who speak a primary language other than English or Spanish
- Patients who are cognitively impaired
- Pregnant women
Who the study is looking for
- In order to be eligible to participate in this study, an individual must meet all of the following criteria:
- Stated willingness to comply with all study procedures and availability for the duration of the study
- Males and females; Age ≥18
- Documented diagnosis of pancreatic cancer
- Access to necessary resources for participating in a technology-based intervention (i.e., computer, smartphone, internet access)
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| UT MD Anderson Coordinator of this site? Confirm its status | Houston | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.