Mobile Health Device Study for Myeloma Patients

CompletedOBSERVATIONAL
Enrollment

40

Participants

Timeline

Start Date

December 31, 2016

Primary Completion Date

November 14, 2024

Study Completion Date

November 14, 2024

Conditions
Multiple MyelomaMyeloma
Interventions
DEVICE

Garmin Vivofit device

Participants will be bio-monitored using the Garmin Vivofit mobile wearable device at baseline (at least 1-7 days prior to treatment initiation) and during induction chemotherapy up to completion of 6 cycles. For those patients continuing with ASCT, patients will be bio-monitored up to 90 days post ASCT.

BEHAVIORAL

Mobile Health quality of life assessements

Trial Locations (5)

10604

Memorial Sloan Kettering Westchester, Harrison

11725

Memorial Sloan Kettering Commack, Commack

Unknown

Memorial Sloan Kettering Basking Ridge, Basking Ridge

07748

Memorial Sloan Kettering Monmouth, Middletown

07645

Memorial Sloan Kettering Bergen, Montvale

All Listed Sponsors
lead

Memorial Sloan Kettering Cancer Center

OTHER

NCT03006315 - Mobile Health Device Study for Myeloma Patients | Biotech Hunter | Biotech Hunter