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Facilitators and Barriers to Cancer Treatment Among Texas Residents

M.D. Anderson Cancer Center logo

M.D. Anderson Cancer Center

Status

Not yet enrolling

Conditions

Cancer

Treatments

Other: Focus Groups
Other: Interviews

Study type

Interventional

Funder types

Other

Identifiers

NCT07105046
2025-0697
NCI-2025-05584 (Other Identifier)

Details and patient eligibility

About

This trial uses semi-structured interviews and focus groups to determine facilitators and barriers of receiving timely cancer treatment among multiple cancers, across multiple insurance types, throughout Texas

Full description

Primary Objectives:

Aim 1: To comprehensively assess barriers to and facilitators of receiving timely cancer treatment, via in-depth telephone interviews among a purposive sample of Texas patients with Stage I-IV breast, colorectal, lung, and prostate cancer and diverse backgrounds.

Aim 2: To generate consensus on barriers and facilitators, as well as their relative importance, via focus groups, among carefully selected Texas patients with Stage I-IV breast, colorectal, lung and prostate cancer and diverse backgrounds,

Enrollment

120 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Aims 1 and 2

In order to be eligible to participate in this study, an individual must meet all of the following criteria:

  • 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 criteria

Aims 1 and 2

An individual who meets any of the following criteria will be excluded from participation in this study:

  • Patients who are cognitively impaired
  • Pregnant women

Trial design

Primary purpose

Health Services Research

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

120 participants in 2 patient groups

Semi-structured Interview
Experimental group
Description:
Participants will be recruited through the Texas Cancer Registry (TCR).
Treatment:
Other: Focus Groups
Online Focus Group
Experimental group
Description:
Participants will be recruited through the Texas Cancer Registry (TCR).
Treatment:
Other: Interviews

Trial contacts and locations

1

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Central trial contact

John Lin, MD

Data sourced from clinicaltrials.gov

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