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Evaluation of Advanced Practice Nurse's Management of Patients With Chronic Myeloid Leukemia (IPA-LMC)

Primary Purpose

Chronic Myelogenous Leukemia - Chronic Phase

Status
Not yet recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
APN and medical management
Medical management
Quality of life assessment
Treatment compliance assessment
Sponsored by
Centre Hospitalier Henri Duffaut - Avignon
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Chronic Myelogenous Leukemia - Chronic Phase focused on measuring Advanced Practice Nursing, Quality of life, Adverse event

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • Centre Hospitalier d'Avignon, Hôpital Henri Duffaut

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

A: IPA group

B: Control group

Arm Description

Patients in arm A are followed by the advanced practice nurse and the hematologist.

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

Outcomes

Primary Outcome Measures

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).
Grade I-II adverse events rate

Secondary Outcome Measures

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).
Grade I-II adverse events rate
Assessment of patient's quality of life
European 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 treatment
GIRERD questionnaire (measures range from 0 to 6. A low score represents a high level of compliance).
Grade > II adverse events rates
Hospitalization rate
Treatment discontinuation rate and/or treatment change rate
Consultation time comparison between advanced practice nurse and hematologist
Molecular response rate assessment

Full Information

First Posted
October 9, 2023
Last Updated
October 13, 2023
Sponsor
Centre Hospitalier Henri Duffaut - Avignon
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1. Study Identification

Unique Protocol Identification Number
NCT06082804
Brief Title
Evaluation of Advanced Practice Nurse's Management of Patients With Chronic Myeloid Leukemia
Acronym
IPA-LMC
Official Title
Evaluation of Advanced Practice Nurse's Management of Patients With Chronic Myeloid Leukemia
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 2023 (Anticipated)
Primary Completion Date
June 2027 (Anticipated)
Study Completion Date
December 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Henri Duffaut - Avignon

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Myelogenous Leukemia - Chronic Phase
Keywords
Advanced Practice Nursing, Quality of life, Adverse event

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
60 patients will be included, these patients will be randomized into two groups.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
A: IPA group
Arm Type
Experimental
Arm Description
Patients in arm A are followed by the advanced practice nurse and the hematologist.
Arm Title
B: Control group
Arm Type
Active Comparator
Arm Description
Patients in arm B are followed by the hematologist only (standard of care).
Intervention Type
Other
Intervention Name(s)
APN and medical management
Intervention Description
Patients are followed by the advanced practice nurse and the hematologist.
Intervention Type
Other
Intervention Name(s)
Medical management
Intervention Description
Patients are followed by the hematologist only (standard of care).
Intervention Type
Behavioral
Intervention Name(s)
Quality of life assessment
Intervention Description
EORTC-QLQ-C30 questionnaire
Intervention Type
Behavioral
Intervention Name(s)
Treatment compliance assessment
Intervention Description
GIRERD questionnaire
Primary Outcome Measure Information:
Title
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).
Description
Grade I-II adverse events rate
Time Frame
Inclusion and 6 months
Secondary Outcome Measure Information:
Title
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).
Description
Grade I-II adverse events rate
Time Frame
6 months and 12 months
Title
Assessment of patient's quality of life
Description
European 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).
Time Frame
Inclusion, 6 months and 12 months
Title
Assessment of patient's compliance to treatment
Description
GIRERD questionnaire (measures range from 0 to 6. A low score represents a high level of compliance).
Time Frame
6 months and 12 months
Title
Grade > II adverse events rates
Time Frame
6 months and 12 months
Title
Hospitalization rate
Time Frame
6 months and 12 months
Title
Treatment discontinuation rate and/or treatment change rate
Time Frame
Every medical consultation, from inclusion to 12 months
Title
Consultation time comparison between advanced practice nurse and hematologist
Time Frame
Every medical consultation, from inclusion to 12 months
Title
Molecular response rate assessment
Time Frame
6 months and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marilyne Grinand, PhD
Phone
(+33)432759392
Email
grinand.marilyne@ch-avignon.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Christine Tosello, APN
Phone
(+33)432759348
Email
ihuel.christine@ch-avignon.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christine Tosello, APN
Organizational Affiliation
Centre Hospitalier d'Avignon, Service d'Oncologie Médicale-Hématologie Clinique
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre Hospitalier d'Avignon, Hôpital Henri Duffaut
City
Avignon
State/Province
Provence-Alpes-Côte d'Azur
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marilyne Grinand, PhD
Phone
(+33)432759392
Email
grinand.marilyne@ch-avignon.fr
First Name & Middle Initial & Last Name & Degree
Christine Tosello, APN
First Name & Middle Initial & Last Name & Degree
Borhane Slama, MD
First Name & Middle Initial & Last Name & Degree
Hacène Zerazhi, MD

12. IPD Sharing Statement

Learn more about this trial

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

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