Active Symptom Monitoring in Patients Undergoing Radiation Therapy for Thoracic Malignancies

Arms (1)

1. label

   Active Symptom Monitoring via Noona

   description

   Participants will undergo a single training session on how to use the Noona software no more than 4-12 weeks before starting therapy. They can start using the software immediately after the training session. Patients will be invited to complete either the Chest Radiotherapy (if radiotherapy alone), Chemotherapy-18 (if chemoradiation therapy), or Bone Radiotherapy (if other) module at baseline, every other week throughout therapy, and during follow up for 90-days. Patients will be encouraged by the treatment team to complete the baseline symptom report prior to starting any therapy and to complete the reports during therapy and in follow up. Patients will also complete the EORTC QLQ-C30 and the NCCN Distress Thermometer at baseline (no more than 12 weeks before starting therapy), within 1 week of completing therapy, and at 90-days follow up. Patients will be encouraged to use Noona's other features beyond invited modules and PRO inventories, such as the diary during the study

   interventionNames

   1. Other: Noona Software

Primary outcomes (2)

1. measure

   Percentage of invited symptom reports completed during the study period

   timeFrame

   Treatment through 90 days of follow-up (estimated to be 5 months)

2. measure