Recruiting

Observational Study

Sponsor:

M.D. Anderson Cancer Center

Code:

NCT06722846

Conditions

Health Options

Strategic Care Planning

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Randomized Case Vignette Study

Study Details

Brief summary:

To learn more about how the delivery of medical information affects therapy choices for participants with advanced forms of cancer.

Conditions

Health Options

Strategic Care Planning

Study ID

NCT06722846

Start date

Nov 21, 2024

Status verified date

Oct, 2026

Completion date

Aug 31, 2028

Anticipated

Primary completion date

Aug 31, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

Diagnosis of advanced solid tumor (i.e. metastatic, relapsed, and/or incurable disease) or aggressive lymphoma.

  • Age 18 or greater
  • Seen at MD Anderson Cancer Center Thoracic and Lymphoma Oncology Clinics for a follow-up visit
  • Been treated with at least 2 lines of palliative systemic cancer therapies

Exclusion Criteria:

  • Diagnosis of cognitive impairment or dementia requiring a surrogate decision maker
  • Non-English speaking

Study Design

Enrollment

400 participants

Anticipated

Interventions and Outcome Measures

Arms

Randomized Case Vignette Study

If participants agree to take part in this study, participants will complete about 16 questionnaires that will have questions about participants quality of life, anxiety, health, and case scenarios that are not real or based on your actual health situation. It should take a bit more than an hour to complete all the questionnaires. If participants find that any of these questions are difficult to read, understand, or otherwise complete; or if they cause distress, participants may ask the study team for clarification, skip the question, or even stop the study at any time.

Additionally, information will be collected from participants medical record about participants health and treatment, as well as participants demographic information (age, race, sex, and so on). Investigators may also ask participants for additional demographic information not found in your medical record.

Interventions

Randomized Case Vignette Study

Particpants will complete about 16 questionnaires that will have questions about particpants quality of life, anxiety, health, andcase scenarios that are not real or based on particpants actual health situation.

Primary outcome measure

  • Overall Survival (OS) [ Time Frame: Through study completion; an average of 1 year. ]

Central Contacts and Locations

Central contacts

David Hui, MD

713-792-6258dhui@mdanderson.org

Locations

MD Anderson Cancer Center

Recruiting

Houston, Texas, United States, 77030

Contacts

David Hui, MD

713-792-6258dhui@mdanderson.org

More Information

Sponsor

M.D. Anderson Cancer Center

Last update posted

Oct 13, 2026

Last verified

Oct, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-10-23. This information was provided to ClinicalTrials.gov by M.D. Anderson Cancer Center on 2026-10-13. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.