Cutting pills, not hope: study probes cancer Patients' views on deprescribing
NCT ID NCT06193083
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looks at how people with advanced cancer feel about stopping or reducing medications that may no longer help. Researchers will interview about 25 patients and survey 300 more to understand their attitudes and beliefs. The goal is to learn what factors influence their views, so doctors can better tailor deprescribing approaches to improve quality of life and reduce side effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could help doctors design better ways to safely reduce medications for advanced cancer patients, potentially improving quality of life.
- What could go wrong
- This is an observational study, not a treatment trial. It only gathers opinions, so it won't directly change care. Results may not apply to all patients.
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.
- Participants
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About 325 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2024
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
We'll be looking at major patients with "solid" cancer in a palliative situation (locally advanced or metastatic cancer, thus requiring palliative care as defined by the World Health Organization), who have at least one PIMs, followed up on an inpatient or outpatient basis, with a life expectancy estimated at less than 1 year by the doctor caring for the patient. To identify whether a patient has at least one PIMs, we will use the STOPPFrail 2 tool . This is a tool developed in geriatrics, validated for a population with an estimated life expectancy of less than 1 year, and which is not specific to oncology. Life expectancy of less than one year will be estimated by the question surprised by the doctor caring for the patient ("Would you be surprised if your patient died within a year?") . We will carry out a multicenter study in oncology and/or palliative care departments of hospitals located in western France.
- 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: * Patient over 18 years of age * Locally advanced or metastatic solid cancer (i.e., palliative care as defined by the World Health Organization) * Life expectancy estimated by the physician at inclusion of less than 1 year (use of surprise question to help clinician estimate life expectancy) * Hospitalized or in consultation * With at least one PIMs (identified using STOPPfrail 2) * Patient not having expressed opposition to participating in the study after receiving information from the physician. For qualitative study patients : \- Patients who have signed an authorization for the recording of their voice during the semi-structured interview for the purpose of written transcription. Exclusion Criteria: * Minor * Major under guardianship, protected person * Patient unable to speak or write French * Patient with impaired judgment, cognitive or sensory impairment that prevents him/her from receiving informed information, answering questionnaires or participating in a study interview.
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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
8 sites. 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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CH ST Nazaire
NOT_YET_RECRUITINGSaint-Nazaire, 44600, France
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CHD Vendée
NOT_YET_RECRUITINGLa Roche-sur-Yon, 85000, France
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CHRU Tours
NOT_YET_RECRUITINGTours, France
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CHU de Nantes
RECRUITINGNantes, 44093, France
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Hospices Civils de Lyon
NOT_YET_RECRUITINGLyon, France
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Hôpital Institut CURIE
NOT_YET_RECRUITINGParis, 75005, France
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Institut de Cancérologie de l'Ouest
NOT_YET_RECRUITINGSaint-Herblain, 44800, France
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USP - Maison de Nicodème
NOT_YET_RECRUITINGNantes, France
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Other studies related to the condition(s) this trial covers.
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- Can a simple mouth rinse ease soreness for patients fed by tube?
- A 45-minute chat could change how advanced cancer patients face tough decisions
- A new care model asks: what matters most to people with diabetic foot ulcers?
- Training healthcare teams to see the whole person behind the illness