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NCT Number: NCT07591480

Barriers And Facilitators To Clinical Trial Enrollment: A Qualitative Study Of Pancreatic Cancer Patients

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

UT MD Anderson

Houston, Texas, 77030, United States

Location contact

Rebecca A Snyder, MD, MPH

CONTACT

[email protected]

713-792-0036

Rebecca A Snyder, MD, MPH

PRINCIPAL_INVESTIGATOR

About this study

Primary Objectives:

The primary objective of this study is to comprehensively assess the barriers to and facilitators of interventional clinical trial enrollment via in-depth interview of participants with pancreatic cancer among diverse backgrounds. The primary outcome will be identification of specific opportunities for improvement to increase study enrollment.

The above aim is part of a long-term multi-armed quality improvement project with the goal of increasing clinical trial enrollment among minority individuals with pancreas cancer. Using the data gained from this project, investigators aim to implement and tailor interventions towards addressing these barriers in conjunction with current scientific evidence. While the QI project is separate from this IRB submission, data gained from this specific research study will be crucial towards steering further improvement efforts.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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)

Exclusion criteria

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

Treatment and study plan

Interviews

Other

Participants will be offered a 30 to 45-minute telephone or video in-depth interview at a specific time convenient to the participants.

Primary outcomes

  1. Questionnaires/Surveys

    Time frame: Through study completion; an average of 1 year

    Identification of specific opportunities for improvement to increase study enrollment.

Study contacts

Contact information is provided by the study sponsor or research team.

Rebecca A Snyder, MD, MPH

CONTACT

[email protected]

(713) 792-0036

Sponsors and collaborators

Lead sponsor

M.D. Anderson Cancer Center

Other

Registry information

Important dates

Study start
2026
Primary completion
2026
Study completion
2028
First posted
May 15, 2026
Registry last updated
May 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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