Actively Recruiting

Age: 18Years +
All Genders
NCT06193083

DEprescribing: Perceptions of PAtients Living With Advanced Cancer

Led by Nantes University Hospital · Updated on 2026-02-11

325

Participants Needed

8

Research Sites

147 weeks

Total Duration

On this page

Sponsors

N

Nantes University Hospital

Lead Sponsor

F

Fondation de France

Collaborating Sponsor

AI-Summary

What this Trial Is About

Polymedication in palliative oncology care is a real public health problem. This phenomenon has been shown to increase the risk of iatrogenesis, reduce patients' quality of life and increase healthcare costs. For many years, health policies have been developed in geriatrics to reduce polymedication through deprescription tools. Recently, palliative care initiatives have been introduced, but without having studied the potential specificities of this population (younger, with a different care dynamic and life trajectory). It is important to better understand this population's perceptions of deprescribing in order to adapt tools/actions to make these approaches more efficient. The primary aim of this study is to investigate patients' perceptions of deprescribing in palliative cancer care, and the secondary aim is to investigate factors that may influence patients' attitudes and beliefs about deprescribing. At the same time, we will study the psychometric properties of the rPATD (Revised Patients' Attitudes Towards Deprescribing) in this population (a standardized questionnaire validated in geriatric medicine to assess patients' perceptions of deprescription).An ancillary study will be carried out to investigate the link between patients' health literacy and their perception of deprescribing (health literacy is defined as the ability to acquire, understand and use information in ways that promote and maintain good health). To meet our objectives, we will conduct a 3-year national, prospective, observational, multicenter study with an exploratory sequential mixed design. The study will comprise an initial qualitative phase. Semi-directed individual interviews using a descriptive approach will be carried out (around 25 patients, over an 8-month period). Following analysis of the qualitative data, we will then carry out a quantitative study to determine the distribution of the different profiles within this population and the factors influencing the perception of deprescription. The self-administered questionnaires, rPATD and BMQ (medication beliefs questionnaire), potentially supplemented by other items following analysis of the qualitative data, will be administered to 300 patients (over a 12-month period).The ancillary study will be carried out during this second phase, using a validated self-questionnaire to assess patients' level of literacy. Thanks to the different results, we will improve our knowledge of the perception of deprescription in palliative oncology care, in order to develop approaches adapted to the specificities of our population to reduce polymedication and thus improve the quality of life of our patients and reduce the risks of iatrogenia.

CONDITIONS

Official Title

DEprescribing: Perceptions of PAtients Living With Advanced Cancer

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient over 18 years of age
  • Locally advanced or metastatic solid cancer (palliative care as defined by WHO)
  • Life expectancy estimated by physician at inclusion less than 1 year
  • Hospitalized or in consultation
  • At least one potentially inappropriate medication (PIM) identified using STOPPfrail 2
  • Patient has not opposed participation after being informed by physician
  • For qualitative study: patient has signed authorization for voice recording during interview
Not Eligible

You will not qualify if you...

  • Minor
  • Major under guardianship or protected person
  • Unable to speak or write French
  • Impaired judgment, cognitive or sensory impairment preventing informed consent, questionnaire completion, or interview participation

AI-Screening

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Trial Site Locations

Total: 8 locations

1

CHD Vendée

La Roche-sur-Yon, France, 85000

Not Yet Recruiting

2

Hospices Civils de Lyon

Lyon, France

Not Yet Recruiting

3

CHU de Nantes

Nantes, France, 44093

Actively Recruiting

4

USP - Maison de Nicodème

Nantes, France

Not Yet Recruiting

5

Hôpital Institut CURIE

Paris, France, 75005

Not Yet Recruiting

6

Institut de Cancérologie de l'Ouest

Saint-Herblain, France, 44800

Not Yet Recruiting

7

CH ST Nazaire

Saint-Nazaire, France, 44600

Not Yet Recruiting

8

CHRU Tours

Tours, France

Not Yet Recruiting

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Research Team

A

Adrien EVIN, MCU-PH

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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