RecruitingNot ApplicableNCT06772181

A Digital Health Intervention to Improve Symptoms and Physical Activity During Breast Radiation

Multicenter Pilot Study: Leveraging Digital Health to Promote Evidence-Based Physical Activity to Improve Symptoms Among Patients Undergoing Radiation for Breast Cancer (PRO-ACTIVE)


Sponsor

University of Washington

Enrollment

40 participants

Start Date

Mar 4, 2025

Study Type

INTERVENTIONAL

Conditions

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.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a digital health program called IM@Home to help breast cancer patients manage fatigue and stay physically active while receiving radiation therapy, using their smartphones or devices. **You may be eligible if...** - You are 18 or older - You have a current breast cancer diagnosis - You are currently receiving radiation therapy with curative intent (including partial breast, whole breast, or regional treatment) - You can understand English or have a caregiver who does - You are willing to sign informed consent **You may NOT be eligible if...** - You do not speak English and do not have an English-speaking caregiver to assist with the program Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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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 Consortium

Seattle, Washington, United States

MultiCare Valley Hospital (Spokane)

Spokane Valley, Washington, United States

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NCT06772181


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