Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Gruppo Italiano Malattie EMatologiche dell'Adulto
The development process will follow the international guidelines published by the EORTC Quality of Life Group (QLG). This process will follow three main phases.
Phase 1 of will deal with the review of the literature, identification of an item list and interviews with experts in the treatment of CML and CML patients (undergoing all possible treatments).
In Phase II the identified issues from Phase I will be worded and translated into possible items for the provisional questionnaire using existing EORTC questionnaires and the EORTC QLG Item Bank.
In the Phase III the provisional CML questionnaire will be pre-tested by to a larger sample of CML patients (not the same patients involved in previous phases) and individual structured interviews will be conducted as well. These latter will identify questions that might be irrelevant or whether there will be additional issues not previously included.
Overall up to 480 patients will be enrolled in this study (up to 180 in phase I and up to 300 in phase III).
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Adult patients (18 years of age or older)
Confirmed diagnosis of Philadelphia chromosome positive CML
Informed consent provided
Patients enrolled in investigational treatment trials are eligible
Ability to speak and read language of the Questionnaire
You may not be if
Freedom from overt cognitive impairment or major psychiatric conditions that may confound HRQOL evaluation
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