🏛️ Verified NIH Record • Updated 2026-03-21

Optimizing Functional Recovery After Breast Cancer Treatment (NCT07489053)

Optimization of a Multicomponent Intervention to Foster Functional Recovery After Breast Cancer Treatment

🟡 Not Yet Recruiting Observational / Diagnostic 🧠 Behavioral & Psychological Program Sponsor: MGH Institute of Health Professions

🩺 Plain-English Summary (8th-Grade Level)

The goal of this clinical trial is to determine the best way to promote participation in vocational, social, physical, and instrumental activities of daily living in people who have completed treatment for early stage breast cancer. The main question it aims to answer is: Which of the intervention components, alone or in combination, most effectively promote participation in vocational, social, physical, and instrumental activities of daily living? Participants will be asked to try one of 8 combination of three intervention components that have been shown to promote activity participation: (1) priority elicitation, (2) education, and (3) guided application involving goal setting, problem-solving and action planning.

Who can join: To join this study, participants generally need to meet the listed inclusion criteria (3 items) and avoid the listed exclusions (5 items).

Location: MGH Institute of Health Professions — Boston, Massachusetts

Age range: 18 Years

🧪 Interventions in This Study

  • Individually tailored education and guided application to promote activity participation (BEHAVIORAL)
  • Individually tailored guided application (BEHAVIORAL)
  • Individually tailored education (BEHAVIORAL)
  • Priority elicitation (BEHAVIORAL)
  • Static education and guided application (BEHAVIORAL)
  • Static guided application (BEHAVIORAL)
  • Static education (BEHAVIORAL)
  • Information (BEHAVIORAL)

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Check every box below. If you can check all of them, you may meet the study's basic screening requirements (final eligibility is confirmed by the site team).

Usually NOT eligible if any of the following apply:

  • Exclusion Criteria:
  • Non-English speaking.
  • Non-correctable hearing loss.
  • Moderate-severe cognitive impairment indicated by a score \< 3 on a 6-item cognitive screener.
  • History of severe mental illness (i.e., schizophrenia, bipolar disorder), current major depressive disorder, active suicidal ideation, or active substance misuse documented within the medical record.

🔍 Extracted verbatim from the official NIH eligibility criteria. Always confirm with the study coordinator.

📍 All Participating Trial Locations (1 Sites)

  • MGH Institute of Health Professions — Boston, Massachusetts

📞 Contact the Study Coordinator

Phone: (617) 643-5372

Email: KLyons2@mghihp.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

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💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗