Understanding Cancer Treatment Experiences in Texas

This study is looking for Texas residents aged 18 and older who have been diagnosed with breast, colorectal, lung, or prostate cancer. The goal is to understand what helps and what makes it difficult to get timely cancer treatment. You would share your experiences through a 30-45 minute phone interview or a 45-60 minute video conference focus group. Researchers want to identify common challenges and helpful factors across different types of cancer and insurance. The study plans to enroll 120 participants and is currently unclear about its recruitment status. The main thing researchers will be looking at is safety and any side effects throughout the study, which is expected to last about one year.

Study design
This study is an interventional study that aims to enroll 120 participants. It uses interviews and focus groups to gather information.
What's involved
You would participate in either a 30-45 minute phone interview or a 45-60 minute video conference focus group.
Compensation
Not stated in the trial record.
Follow-up
Safety and adverse events will be measured through study completion, which is an average of 1 year.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07105046

Facilitators and Barriers to Cancer Treatment Among Texas Residents

Not Yet Recruiting
NAAges 18+InterventionalHealth services
M.D. Anderson Cancer Center
~120 participants
Updated 2026-03-02 on ClinicalTrials.gov
What's tested:InterviewsFocus Groups

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
1. Safety and Adverse Events (AEs)
Measured over Through study completion; an average of 1 year
Cancer
1 sites across 1 states
Texas1
  • John Lin, MD · PRINCIPAL_INVESTIGATOR · M.D. Anderson Cancer Center

Opens a ready-to-send draft in your own email app — review before sending.

Do you actually qualify for this trial?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

Verbal consent will be obtained
Stated willingness to comply with all study procedures and lifestyle considerations and availability for the duration of the study
Males and females; Age ≥ 18 years old
Documented diagnosis of breast, colorectal, lung, and prostate cancer patients, stage I-IV
Either English or Spanish-speaking

Exclusion

Patients who are cognitively impaired
Pregnant women
  • 1. Safety and Adverse Events (AEs)Through study completion; an average of 1 year

    Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0