Condition: Multiple Myeloma · Refractory Multiple Myeloma · Sponsor: Pack Health
This descriptive study aims to evaluate the experience of adults with relapsed or refractory multiple myeloma receiving standard of care isatuximab-irfc through collection of quantitative, qualitative and wearable data. Fifty adults with relapsed or refractory multiple myeloma receiving standard of care isatuximab-irfc will be enrolled across 2 sites, The University of California San Francisco and The University of Texas MD Anderson Cancer Center. Consented participants will be enrolled in a 3-month digital health coaching program through which electronic patient reported outcomes and wearable activity data will be collected. Outcomes include treatment experience, quality of life, financial toxicity, treatment adherence, symptom burden and health self-efficacy. These will be captured by patient reported outcome measures including the Patient's Qualitative Assessment of Treatment- Real World (PQAT-RW), Patient Global Impression of Change/Severity (PGIC/S), European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC-QLQ-C30), Quality of Life Questionnaire Multiple Myeloma (QLQ-MY20), and the European QoL-5 Dimensions (EQ5D), Cancer Behavior Inventory-Brief Form (CBI-B), Center for Adherence Support Evaluation (CASE) Medication Adherence Index, Comprehensive Score for Financial Toxicity (COST) Instrument. Clinical data, including treatment history, healthcare utilization, and co-morbidities, as well as demographic data will be collected via t…
This description comes directly from the study's public registry record.
Kelly J Brassil, PhD · 205-721-7542 · dgxpharesearch@questdiagnostics.com
Jennifer Loftis, DNP · 205-721-7542 · dgxpharesearch@questdiagnostics.com
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| The University of Texas MD Anderson Cancer Center | Houston, Texas, United States | Active Not Recruiting |
| University of Washington | Seattle, Washington, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05053607