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Spots Global Cancer Trial Database for Evaluation of Advanced Practice Nurse's Management of Patients With Chronic Myeloid Leukemia

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Trial Identification

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

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

Study ID: NCT06082804

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.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Centre Hospitalier d'Avignon, Hôpital Henri Duffaut, Avignon, Provence-Alpes-Côte d'Azur, France

Contact Details

Name: Christine Tosello, APN

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

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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