Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06772181

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

Led by University of Washington · Updated on 2026-01-23

40

Participants Needed

2

Research Sites

82 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 63 18 years old
  • Ability to understand English or has a caregiver who understands English
  • Ability and willingness to sign a written informed consent document, virtually or in-person
  • Current breast cancer diagnosis
  • Currently receiving radiation with curative intent (partial breast, whole breast, or regional nodal radiation)
Not Eligible

You will not qualify if you...

  • Non-English speaking patients preventing participation in the IM@Home program

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Fred Hutch/University of Washington Cancer Consortium

Seattle, Washington, United States, 98109

Actively Recruiting

2

MultiCare Valley Hospital (Spokane)

Spokane Valley, Washington, United States, 99216

Actively Recruiting

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Research Team

E

Erin Gillespie, MD, MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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