CompletedNot applicableNCT05634551
Official study title

Perceptions on Expected Outcomes of Immunotherapy in Advanced Cancer Patients With Poor Performance Status

Study summary

To better understand your feelings and expectations about immunotherapy

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Key things to know

Main goalNot specified

This describes the study’s primary purpose.

What is being studiedQuestionnaires and Interview

The study team can explain what participation involves.

Who it may be forNon-small cell lung cancer (NSCLC)

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Aug 6, 2024 · Source: ClinicalTrials.gov

Is enrollment open?Completed

Ask the study team to confirm whether enrollment is open.

What kind of study?Not applicable

Observational

Where is it offered?1 U.S. location

Locations may change over time.

Who runs it?M.D. Anderson Cancer Center

Study sponsor

01
Study overview

What this study is about

Purpose
Not specified
Study type
Observational
Phase
Not applicable
Sponsor
M.D. Anderson Cancer Center
Interventions being studied
Behavioral: Questionnaires; Behavioral: Interview
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.

Requirements people may need to meetInclusion criteria

1. Patients being considered for or within 2 months of starting immunotherapy for advanced cancer 2. Patient ≥18 years of age 3. ECOG ≥2 4. Cognitively able to understand consent and complete questionnaire as determined by the interviewer at the time of study enrollment 5. English speaking 6. Willing to participate in the study and sign informed consent 7. The study will include medical oncologists that treat advanced cancers

Reasons someone may not be able to joinExclusion criteria

1. Treatment for curative intent 2. Presence of Delirium (as determined by score \>13 on MDAS 46, appendix A)

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • M D Anderson Cancer CenterHouston, Texas

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Aug 6, 2024. Always confirm current availability with the study team.

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