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
Recruiting now · Not applicable
Conditions studied: Lung Carcinoma
In brief
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.
Key facts
- Study ID
- NCT06196008
- Run by
- City of Hope Medical Center
- People needed
- 382
- Starts
- 2023-12-05
- Expected to finish
- 2028-05-16
- Last updated by the study team
- 2026-03-05
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- PATIENT: Documented informed consent of the participant and/or legally authorized representative
- PATIENT: Agreement to allow the use of preoperative chest CT scan for exploratory analysis, if available
- PATIENT: Agreement to wear pedometer during study duration
- If unwilling, exceptions may be granted with study primary investigator (PI) approval
- PATIENT: Age >= 65 years
- PATIENT: Ability to read and understand English or Spanish and willingness to complete participant-reported outcomes and assessments
- PATIENT: Diagnosis of lung cancer or presumed lung cancer (as determined by surgeons) in patient
- PATIENT: Scheduled to undergo lung surgery for lung cancer or suspected lung cancer with curative intent (neoadjuvant therapy allowed)
- PATIENT: Adults lacking capacity to consent in the opinion of the attending surgeon will not be enrolled
- FCG: Documented informed consent of the participant and/or legally authorized representative
- FCG: Age >= 18
- FCG: Ability to read and understand English or Spanish and willingness to complete participant-reported outcomes and assessments
- FCG: Adults lacking capacity to consent in the opinion of the attending surgeon will not be enrolled
You may not qualify if…
- PATIENT: Lung surgery is scheduled in less than 14 calendar days from the time of registration
- PATIENT: Prospective participants who, in the opinion of the investigator, may not be able to comply with all study procedures (including exercise program and compliance issues related to feasibility/logistics)
- FCG: Prospective participants who, in the opinion of the investigator, may not be able to comply with all study procedures (including exercise program and compliance issues related to feasibility/logistics)
Where it is running
- University of California — Davis, California, United States (enrolling)
- City of Hope Medical Center — Duarte, California, United States (enrolling)
- City of Hope at Irvine Lennar — Irvine, California, United States (enrolling)
- Standard University — Stanford, California, United States (enrolling)
- City of Hope at Upland — Upland, California, United States (enrolling)
- Yale New Haven Medical Center — New Haven, Connecticut, United States (enrolling)
- Moffitt Cancer Center — Tampa, Florida, United States (enrolling)
- City of Hope at Georgia - Atlanta — Newnan, Georgia, United States (enrolling)
- Northwestern University — Evanston, Illinois, United States (enrolling)
- Massachusetts General Hospital (MGH) / Harvard — Boston, Massachusetts, United States (enrolling)
- Lahey Hospital & Medical Center — Burlington, Massachusetts, United States (enrolling)
- University of Mississippi Medical Center — Jackson, Mississippi, United States (enrolling)
- Duke University — Durham, North Carolina, United States (enrolling)
- Ohio State University — Columbus, Ohio, United States (enrolling)
- Baptist Clinical Research Institute — Memphis, Tennessee, United States (enrolling)
- MD Anderson Cancer Center — Houston, Texas, United States (enrolling)
Full record on ClinicalTrials.gov
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