Lymphoma Multiple Myeloma
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: In order to be eligible to participate in this study, a subject must meet all of the following criteria: - Patients diagnosed with either HL, NHL, CLL or MM - 18 years or older - Able to fill out questionnaires Dutch (in terms of language skills and cognitive abilities).
Exclusion criteria
Exclusion criteria: Patients with severe psychopathology or dementia, and patients in transition to terminal care will be excluded from the study. We will only have our questionnaire in Dutch, so patients who cannot read Dutch will be unable to complete the questionnaire.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary: HRQoL (EORTC QLQ-C30) and disease specific HRQoL/symptoms (EORTC QLQ-LYMPH32 or EORTC QLQ-MY20 + 2 single items from EORTC item library) | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary: neuropathy (single item from EORTC item library), sexual functioning/intimacy (5 single items from EORTC item library), anxiety and depressive symptoms (HADS), side effects (PRO-CTC-AE), personality (LOT-R and BFI), self-management (HEIQ), coping (SE7), health status (EQ-5D), therapy adherence (MARS) and health-care use. | — |
Countries
Netherlands