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The goal of this laboratory research study is to learn about symptoms and activity levels of patients with OPSCC that receive IMPT or TORS.
Full description
Baseline Visit:
If participant agrees to take part in this study, they will complete the following tests and procedures at their baseline visit. This baseline visit will take place before participant's treatment with IMPT or TORS:
It should take about 30 minutes to complete all of the questionnaires.
As part of participant's baseline visit, information below will be collected from their medical record:
Activity Bands:
The study staff will either give participant an activity band at their baseline visit or they will be mailed an activity wristband. Participant will be asked to wear the band 24 hours a day for 1 week leading up to all study visits. The wristband will record how active participant is and how much they sleep. The study staff will show participant how to wear and use the wristband.
Study Visits:
Participant will complete the following study procedures after they complete treatment with either IMPT or TORS, and at 3 and 6 months after that.
IMPT patients only:
If participant is receiving IMPT, they will complete the questionnaires they completed at the baseline visit once a week while they are receiving treatment.
Length of Study:
Participant's active participation in this study will be over after the 6 month study visit.
Participant will return the wristband to the study staff after their participation is over. If participant loses or damages the wristband while they are on study, another one will be provided to them at no cost.
This is an investigational study.
Up to 44 participants will take part in this study. All will be enrolled at MD Anderson.
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N/A
44 participants in 2 patient groups
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Central trial contact
Neil Gross, MD
Data sourced from clinicaltrials.gov
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