Multiple Myeloma Clinical Trial
Official title:
Quality of Life and Psychological Distress in Patients With Multiple Myeloma and Their Caregivers
The main purpose of this study is to examine differences in quality of life and psychological
distress for both Multiple Myeloma patients receiving treatment and their caregivers and to
assess patient and caregiver prognostic understanding (understanding of the likely course of
a disease over time) of Multiple Myeloma to guide development of more personalized treatment
plans.
This study looks to further understand quality of life changes throughout multiple myeloma
therapy for both patients and caregivers to help determine ways to improve patient and
caregiver understanding of illness and in turn, tailor customized treatment that best aligns
with patient preferences.
The study will use a series of questionnaires to measure quality of life, mood, coping
strategies, and prognostic understanding.
This research study's procedures include screening for eligibility, participant designation
of a caregiver and a series of questionnaires.
- It is expected that about 180 people undergoing treatment for multiple myeloma and up to
180 of their caregivers will take part in this research study.
-- The questionnaires are completed one time only and measure quality of life, mood, coping
strategies, and prognostic understanding and can be completed in the hospital, clinic, over
the email, or telephone with assistance provided as needed.Questionnaires take approximately
20 minutes to complete.
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