New program aims to give veterans with advanced cancer a stronger voice in their End-of-Life care
NCT ID NCT07690904
First seen Jul 08, 2026 · Last updated Jul 30, 2026 · Updated 4 times
Summary
This study tests a program that pairs veterans with advanced cancer with a lay health worker who helps them discuss their goals and preferences for care with their doctors. The goal is to increase the number of veterans who have these important conversations and document their wishes, reducing unwanted intensive treatments at the end of life. The trial involves 200 veterans across 7 VA sites and compares the program to usual care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- lay health worker-led educational and support intervention
- What this could lead to
- If successful, this approach could help more veterans with advanced cancer have important conversations about their care preferences, potentially reducing unwanted aggressive treatments at the end of life.
- What could go wrong
- The trial is relatively small (200 participants) and tests a behavioral intervention, so results may not apply broadly. It also relies on self-reported outcomes, which can be subjective.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2031
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a US federal agency other than the NIH.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Veteran patients with diagnosis of a solid malignancy with any cancer stage * English or Spanish-speaking * Can self-administer questionnaires in English or Spanish * Valid telephone number * Receiving oncology care at one of 7 sites * Receiving systemic anti-cancer therapy, defined as oral, injection, or intravenous therapy * chemotherapy * hormone therapy * targeted therapy * or immunotherapy defined by the National Cancer Institute A to Z List of Cancer Drugs) * CAN risk score ≥98th percentile (may be adjusted after examining site-level CAN performance) Exclusion Criteria: * No capacity to consent * Actively receiving hospice care
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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VA Palo Alto Health Care System, Palo Alto, CA
Palo Alto, California, 94304-1207, United States
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