Quality of Life and Care Organization of Patients With Chronic Myeloid Leukemia in the Lombardy Hematology Network

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity of Milano Bicocca

About this trial

The primary objective of the study is to assess the impact of the organizational model of the hematology center on the quality of life of patients with CML estimated through standardized tools (EORTC QLQ-30, CML24) and through the patient's opinion regarding aspects of the quality of care.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Subjects aged 18 years or older.

Subjects diagnosed with Chronic Myeloid Leukemia.

Subjects diagnosed with CML under care at the hematology outpatient clinics of the 21 REL centers.

Subjects followed at the reference hematology center for a minimum of 6 months.

Disqualifiers

Subjects who have not given consent to participate in the study.

Subjects who do not meet the inclusion criteria.

Trial population

Subjects diagnosed with Chronic Myeloid Leukemia.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Quality of Life Assessed Through Standardized Questionnaires (EORTC QLQ-C30)

Quality of life in CML patients will be assessed using the validated EORTC QLQ-C30 (European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30). This instrument evaluates multiple domains of physical, emotional, and social functioning, as well as general cancer-related symptoms. The questionnaire consists of 30 items, with 28 items scored from 1 (minimum functioning/symptom presence) to 4 (maximum functioning/symptom presence), and 2 items scored from 1 to 7. Raw scores are transformed according to EORTC guidelines onto a standardized scale from 0 to 100, where 0 represents the lowest functioning or symptom level and 100 represents the highest functioning or symptom level. For functional scales and the global health status, higher scores indicate better quality of life, whereas for symptom scales, higher scores indicate worse quality of life.

Time frame
One-time measurement at baseline during the 12-month enrollment period
2

Quality of Life Assessed Through Standardized Questionnaires (EORTC QLQ-CML24)

Quality of life in CML patients will also be assessed using the validated EORTC QLQ-CML24 (European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire for Chronic Myeloid Leukemia 24), which measures symptoms and functioning specifically related to CML. This questionnaire includes 24 items scored from 1 to 4. Raw scores are transformed according to EORTC guidelines onto a standardized 0 to 100 scale, with 0 indicating the lowest and 100 the highest level of functioning or symptom presence. Higher scores on functional scales correspond to better quality of life, while higher scores on symptom scales correspond to worse quality of life.

Time frame
One-time measurement at baseline during the 12-month enrollment period.

Secondary outcomes

1

Evaluation of Different Organizational and Care Models of Hematology Outpatient Clinics for CML Patients

Assessment of how different organizational models of hematology outpatient clinics (e.g., structure, workflow, resource allocation) influence the patient experience and perceived quality of care within the REL network. Data for these outcomes will be collected through study-specific questionnaires administered to patients.

Time frame
One-time measurement at baseline during the 12-month enrollment period.
2

Evaluation of Strengths and Weaknesses of Different Outpatient Organizational Settings

Comparison of perceived strengths and weaknesses of various organizational settings, such as large vs. small centers and dedicated outpatient clinics vs. time-slot-based care. Data for these outcomes will be collected through study-specific questionnaires administered to patients.

Time frame
One-time measurement at baseline during the 12-month enrollment period.
3

Evaluation of Factors Affecting Daily Life in CML Patients

Assessment of the impact of CML and its management on daily living activities, autonomy, and social participation, as reported by patients. Data for these outcomes will be collected through study-specific questionnaires administered to patients.

Time frame
One-time measurement at baseline during the 12-month enrollment period.
4

Evaluation of Emotional Well-being in CML Patients

Assessment of the emotional and psychological status of patients using validated tools (e.g., emotional functioning domain of EORTC QLQ-C30). Data for these outcomes will be collected through study-specific questionnaires administered to patients.

Time frame
One-time measurement at baseline during the 12-month enrollment period.

Other outcomes

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