Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06797037

Proof of Concept to Assess the Feasibility of a Decentralised Pathway Coordinated by the Advanced Practice Nurse for Patients Receiving Oral Treatment for Cancer or Malignant Haemopathy (ACCELER PLATFORM)

Led by Institut Claudius Regaud · Updated on 2025-05-20

33

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is an open-label, single-centre, category 2 "Jardé Law" proof-of-concept study designed to demonstrate the feasibility of a decentralised care pathway for patients with cancer or haematological malignancies receiving oral treatment. The study will be conducted on a population of 33 patients. In current practice, patients with certain solid cancers or haematological malignancies may be prescribed oral chemotherapy on a retroceded basis. In these cases, the oncologist (coordinating investigator) sees the patient for a consultation every 3 cycles to prescribe/renew the treatment for approximately 3 months. Every month, the patient returns to the centre to have the treatment dispensed by the hospital pharmacy. No medical consultation is associated with this visit. In this study, it is proposed to decentralise the delivery of treatment to these patients by introducing two visits to the patient's home by a service-providing nurse. The decentralised patient pathway will be organised and monitored by the Advanced Practice Nurse (APN) at the investigating centre, who will be responsible in particular for coordination with the service-providing nurse and the hospital pharmacy.

CONDITIONS

Official Title

Proof of Concept to Assess the Feasibility of a Decentralised Pathway Coordinated by the Advanced Practice Nurse for Patients Receiving Oral Treatment for Cancer or Malignant Haemopathy (ACCELER PLATFORM)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient over 18 years old
  • Diagnosed with solid cancer or haematological malignancy and receiving oral retroceded therapy as part of standard care
  • Performance status (ECOG) between 0 and 2
  • Able to be contacted by telephone for follow-up by the Advanced Practice Nurse
  • Willing to receive two home visits by a nurse within 6 months of inclusion
Not Eligible

You will not qualify if you...

  • Pregnant or breastfeeding
  • Psychological, family, geographical, or social issues that may prevent informed consent or adherence to the study
  • Being deprived of liberty by legal or administrative decision, or under guardianship

AI-Screening

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Trial Site Locations

Total: 1 location

1

Institut Universitaire du Cancer de Toulouse - Oncopole

Toulouse, France, 31059

Actively Recruiting

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Research Team

P

Pierre BORIES

CONTACT

A

Alexandra LAMBERT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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