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
Trial Details
| Condition | Breast Carcinoma |
| Intervention | IM@Home Program; Medical Device Usage and Evaluation; Questionnaire Administration; Interview |
| Phase | NA |
| Status | Active |
| Participants | 40 |
| Est. Completion | 30 Apr 2026 |
| Last Updated | 26 May 2026 |
Primary Outcome
Proportion of eligible patients that consent to the screening registry (Feasibility); Proportion of patients with fatigue or other comorbid symptoms enrolling to the Integrative Medicine at Home (IM@Home) virtual intervention (Acceptability); Proportion of patients enrolling in IM@Home virtual intervention that report favorable implementation outcomes (Appropriateness)
Eligibility Criteria
Inclusion Criteria
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.
Trial Sites
Countries
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