Multicenter Pilot Study: Leveraging Digital Health to Promote Evidence-Based Physical Activity to Improve Symptoms Among Patients Undergoing Radiation for Breast Cancer (PRO-ACTIVE)
University of Washington
Summary
This clinical trial evaluates a digital health intervention for improving symptoms and physical activity among patients with breast cancer undergoing radiation. Cancer-related fatigue is common and strongly associated with quality of life during and after treatment. Increasing emphasis on early symptom detection and management has prompted initiatives to collect patient-reported fatigue from all patients during treatment. Mind-body interventions including physical activity and yoga are recommendations to treat fatigue and comorbid (coexisting) symptoms. Lower socioeconomic status has not only been associated with higher rates of physical inactivity but also with perceptions that it could negatively impact fatigue and quality of life during treatment. A virtual mind-body program called Integrative Medicine at Home (IM@Home) includes cardio fitness and yoga classes in a bundled intervention that has demonstrated decreased fatigue, depression, insomnia, and symptom distress among patients undergoing breast radiation. The IM@Home program may also increase physical activity among patients with breast cancer undergoing radiation.
Description
OUTLINE: REGISTRY: Patients receive a FitBit activity tracker and complete patient-reported outcomes (PRO) surveys every 2 weeks (Q2W) to monitor fatigue, comorbid symptoms, and physical activity during and immediately after radiation therapy. Patients with presence of self-reported symptoms or physical inactivity at baseline and/or from any Q2W PRO surveys are then invited to participate and register for IM@Home. INTERVENTION: Patients participate in the IM@Home program consisting of 20+ live, virtual mind-body and fitness classes ranging from yoga and tai chi to dance cardio, guided medita…
Eligibility
- Age range
- 18+ years
- Sex
- All
- Healthy volunteers
- No
Inclusion Criteria: * Age ≥ 18 years old. * Ability to understand English, or has a caregiver who understands English. * Ability to understand and willingness to sign a written informed consent document, virtually or in-person. * Current breast cancer diagnosis. * Currently receiving radiation with curative intent (including partial breast, whole breast, or regional nodal radiation). Exclusion Criteria: * Patients who are non-English speaking that would prevent their participation in IM@Home.
Interventions
- BehavioralIM@Home Program
Participate in the IM@Home program delivered via Zoom
- OtherMedical Device Usage and Evaluation
Wear a FitBit activity tracker
- OtherQuestionnaire Administration
Ancillary studies
- OtherInterview
Ancillary studies
Locations (2)
- Fred Hutch/University of Washington Cancer ConsortiumSeattle, Washington
- MultiCare Valley Hospital (Spokane)Spokane Valley, Washington