Telephone-based Physical Activity Coaching or Self Monitored Physical Activity to Improve Physical Function in Older Adults Who Are Undergoing Surgery for Lung Cancer and Their Caregivers (NCT06196008)
SR2204: A Randomized Phase III Trial of a Perioperative Physical Activity Intervention in Older Adults With Lung Cancer and Their Family Caregivers
🩺 Plain-English Summary (8th-Grade Level)
This clinical trial compares telephone-based physical activity coaching to self monitored physical activity for improving physical function in older adults who are undergoing surgery for lung cancer and their caregivers. Lung cancer surgery in older adults is associated with functional declines and unique challenges. Performing physical activity around the time of surgery has been shown to improve functional outcomes in patients and exercise programs delivered via telehealth may improve access and convenience for patients and minimize participant burden. Telephone-based physical activity coaching may improve physical functioning for older adults with lung cancer who are undergoing surgery.
Who can join: Review the eligibility criteria below.
Location: University of California — Davis, California
Age range: 18 Years
🧪 Interventions in This Study
- Educational Intervention (OTHER)
- Educational Intervention (OTHER)
- Exercise Intervention (OTHER)
- Medical Device Usage and Evaluation (OTHER)
- Physical Performance Testing (OTHER)
- Quality-of-Life Assessment (OTHER)
- Questionnaire Administration (OTHER)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (16 Sites)
- University of California — Davis, California
- City of Hope Medical Center — Duarte, California
- City of Hope at Irvine Lennar — Irvine, California
- Standard University — Stanford, California
- City of Hope at Upland — Upland, California
- Yale New Haven Medical Center — New Haven, Connecticut
- Moffitt Cancer Center — Tampa, Florida
- City of Hope at Georgia - Atlanta — Newnan, Georgia
- Northwestern University — Evanston, Illinois
- Massachusetts General Hospital (MGH) / Harvard — Boston, Massachusetts
- Lahey Hospital & Medical Center — Burlington, Massachusetts
- University of Mississippi Medical Center — Jackson, Mississippi
- Duke University — Durham, North Carolina
- Ohio State University — Columbus, Ohio
- Baptist Clinical Research Institute — Memphis, Tennessee
- MD Anderson Cancer Center — Houston, Texas
📞 Contact the Study Coordinator
Phone: (626) 471-7100
Email: draz@coh.org
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
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.