Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Hematopoietic and Lymphoid Cell Neoplasm
  • Malignant Solid Neoplasm
Type
Interventional
Phase
Phase 2
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: None (Open Label)Primary Purpose: Health Services Research

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

OUTLINE: Patients complete questionnaires, undergo 3 24-hour dietary recalls over 3 days, and wear an Actigraph over 7 continuous days. After 2-3 weeks, patients receive a FitBit to monitor physical activity. Patients are then assigned to 1 of 2 arms. ARM I: Patients attend 6 online nutrition and ph...

OUTLINE: Patients complete questionnaires, undergo 3 24-hour dietary recalls over 3 days, and wear an Actigraph over 7 continuous days. After 2-3 weeks, patients receive a FitBit to monitor physical activity. Patients are then assigned to 1 of 2 arms. ARM I: Patients attend 6 online nutrition and physical activity (PA) education classes, cooking sessions, and participate in physical activities over 90 minutes each. Patients wear a FitBit and Actigraph to monitor physical activity. ARM II: Patients receive motivational text messages 2-3 times per week and access to a nutrition website for 3 months. Patients wear a FitBit and Actigraph to monitor physical activity. After completion of study, patients are followed up periodically.

Tracking Information

NCT #
NCT04081298
Collaborators
National Cancer Institute (NCI)
Investigators
Principal Investigator: Rachel Ceballos Fred Hutch/University of Washington Cancer Consortium