Randomized Study of Digital Life Coaching in Myeloma Patients Undergoing Transplantation

This is a single-center, Phase II randomized study of MM patients comparing 16 weeks of DLC access versus quasi-usual care (quasi-usual because both arms will receive generic wellness-related electronic handouts alongside requests for patient-reported outcome (PRO) assessments). Primary Objective: To evaluate DLC's impact on B/Z drug usage (excluding lorazepam prescribed for chemotherapy-induced nausea/vomiting, or CINV) Secondary Objectives: 1. To evaluate DLC's impact on patient-reported general quality of life every 1-2 weeks 2. To evaluate DLC's impact on patient-reported psychosocial distress every 1-2 weeks 3. To evaluate DLC's impact on patient-reported insomnia every 1-2 weeks Exploratory Objectives: 1. To explore DLC's impact on rates of communications between patients and their treatment teams 2. To explore DLC's impact on clinical outcomes Participants may continue study treatment (DLC platform access) for 16 weeks from the time of initiating treatment. Participants will not be contacted by the DLC platform vendor after this point. Patients will be followed up at Day +101 after SCT, corresponding to approximately 3 months after SCT.