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Evaluation of Advanced Practice Nurse's Management of Patients With Chronic Myeloid Leukemia

Evaluation of Advanced Practice Nurse's Management of Patients With Chronic Myeloid Leukemia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06082804
Acronym
IPA-LMC
Enrollment
60
Registered
2023-10-13
Start date
2023-11-29
Completion date
2027-12-01
Last updated
2026-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Myelogenous Leukemia - Chronic Phase

Keywords

Advanced Practice Nursing, Quality of life, Adverse event

Brief summary

Chronic Myeloid Leukemia (CML) affects 820 people per year in France (2018), half of them are older than 60 years old. Tyrosine Kinase Inhibitors (TKI) are new kind of targeted therapy whose efficiency allow for a high rate of complete molecular response, leading to a disruption of treatment under certain conditions. Optimizing CML treatment is a major concern, particularly for adverse events management, treatment compliance and therapeutic response. Multiple studies demonstrated that grade ≤ II adverse events are most likely to be under reported by patients and clinicians. Although these adverse events are mostly reported by clinical examination, needing minimal treatment. These toxicities could alter daily and domestic living activities, potentially impacting treatment compliance and therapeutic response. Therefore, early detection of these adverse events is a major challenge for the prognosis and care of CML. The Advanced Practice Nurse (APN), a new health care professional, acquired the skills needed to independently follow, manage and care the patients with medical approvals. At international level, many studies, in oncology and in others domains, have been done to demonstrate the added value of the APN, particularly in improving patient's quality of life, management, care of drug-induced adverse events and treatment compliance. In France, because of the recentness of the profession, only few studies were have been conducted. The goal of this study is to demonstrate the benefit of APN in clinical follow-up, quality of life, treatment compliance, and therapeutic response of CML patients. These effects could be managed thanks to early detection and management of ≤ grade II adverse events during consultation, in partnership with the patients, and in collaborative working.

Interventions

OTHERAPN and medical management

Patients are followed by the advanced practice nurse and the hematologist.

OTHERMedical management

Patients are followed by the hematologist only (standard of care).

BEHAVIORALQuality of life assessment

EORTC-QLQ-C30 questionnaire

BEHAVIORALTreatment compliance assessment

GIRERD questionnaire

Sponsors

Centre Hospitalier Henri Duffaut - Avignon
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

60 patients will be included, these patients will be randomized into two groups.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years old. * CML patient in chronic phase, eligible for oral therapy. * Newly diagnosed CML and/or initiating oral therapy : * Patient changing treatment for non-response or loss of therapeutic response or toxicities, on the condition that these toxicities are resolved or grade I maximum at the time of inclusion. * Newly start of oral therapy. * Patient eligible to a follow-up by an advanced practice nurse. * Patient capable to understand french and complete a questionnaire.

Exclusion criteria

* Patient that had a follow-up \> 3 months by an advanced practice nurse for CML before inclusion. * Patient changing treatment for toxicities, if these toxicities are still \> grade I at inclusion. * Patient enrolled in another interventional research protocol for CML. * Pregnant women. * Patient under legal protection, deprived of liberty or unable to be included in a research protocol.

Design outcomes

Primary

MeasureTime frameDescription
Evaluate the role of the advanced practice nurse in early detection of grade I-II adverse events during care and management of Chronic Myeloid Leukemia compared to standard of care (hematologist only).Inclusion and 6 monthsGrade I-II adverse events rate

Secondary

MeasureTime frameDescription
Evaluate the role of the advanced practice nurse in early detection of grade I-II adverse events during care and management of Chronic Myeloid Leukemia compared to standard of care (hematologist only).6 months and 12 monthsGrade I-II adverse events rate
Assessment of patient's quality of lifeInclusion, 6 months and 12 monthsEuropean Organization for Research and Treatment of Cancer Quality-of-Life-Questionnaire-Core-30 : EORTC-QLQ-C30 (composed of both multi-item scales and single-item measures : 5 functional scales, 3 symptom scales, 6 single items and a global health status. All of the the scales and single-item measures range in score from 0 to 100. A high scale score represents a higher response level. ie : A high score for a functional scale represents a high level of functioning, a high score for the global health status represents a high quality of life but a high score for a symptom scale or a single item represents a high level of symptomatology).
Assessment of patient's compliance to treatment6 months and 12 monthsGIRERD questionnaire (measures range from 0 to 6. A low score represents a high level of compliance).
Grade > II adverse events rates6 months and 12 months
Hospitalization rate6 months and 12 months
Treatment discontinuation rate and/or treatment change rateEvery medical consultation, from inclusion to 12 months
Consultation time comparison between advanced practice nurse and hematologistEvery medical consultation, from inclusion to 12 months
Molecular response rate assessment6 months and 12 months

Countries

France

Contacts

CONTACTMarilyne Grinand, PhD
grinand.marilyne@ch-avignon.fr(+33)432759392
CONTACTChristine Tosello, APN
ihuel.christine@ch-avignon.fr(+33)432759348
PRINCIPAL_INVESTIGATORChristine Tosello, APN

Centre Hospitalier d'Avignon, Service d'Oncologie Médicale-Hématologie Clinique

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 5, 2026