Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Decentralized care pathway for cancer patients receiving oral treatment

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)

Run by Institut Claudius Regaud · NCT06797037 · Data updated 2026-11-12

This study is testing a new way for cancer patients on oral chemotherapy to receive care at home from a nurse instead of going to the hospital, to see if it makes them happier and helps them stick to their treatment.

More Solid Cancer trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment33 (estimated)
SponsorInstitut Claudius Regaud
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Toulouse)
StatusRecruiting
StartedMay 19, 2025
Main results expectedNovember 19, 2028
Study endsNovember 19, 2028
Registry record updatedSeptember 2, 2026
Trial IDNCT06797037 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include adults over 18 with solid cancers or haematological malignancies who are currently receiving oral retroceded therapy.

Probably not a fit

Patients who are pregnant, breastfeeding, or have conditions that hinder compliance with the study protocol may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This proof-of-concept study aims to assess the feasibility of a decentralized care pathway for patients with solid cancers or haematological malignancies who are receiving oral chemotherapy. The study will involve 33 patients and will replace traditional hospital visits with home visits by an advanced practice nurse to enhance patient care and convenience. The goal is to evaluate whether this approach can improve treatment adherence and patient satisfaction while maintaining safety and efficacy.

Why it matters

Potential benefit: If successful, this approach could provide a more convenient and patient-centered method of delivering oral chemotherapy.

How similar studies have gone: While this approach is innovative, similar decentralized care models have shown promise in improving patient outcomes in other settings.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Patient over 18.
2. A patient with solid cancer or haematological malignancy receiving oral retroceded therapy as part of standard management.
3. Patient with a performance index (ECOG): 0-2.
4. Patient contactable by telephone for follow-up by the Advanced Practice Nurse.
5. Patient willing to make two home visits within 6 months of inclusion.

Exclusion Criteria:

1. Pregnant or breast-feeding patient.
2. Any psychological, family, geographical or social condition which, in the judgement of the oncologist, could potentially prevent the collection of informed consent or hinder compliance with the study protocol.
3. Patients deprived of their liberty by administrative or legal decision, or patients under guardianship.

Where it's running

  • Institut Universitaire du Cancer de Toulouse - Oncopole
    Toulouse, France
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.