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
SR2204: A Randomized Phase III Trial of a Perioperative Physical Activity Intervention in Older Adults With Lung Cancer and Their Family Caregivers
Who can join
As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.
- Age
- 18 Years and older
- Sex
- All sexes
- Healthy volunteers
- Accepted
- Compensation
- Not stated
Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.
What to expect
No one can promise a trial will help you personally — that is what the research is trying to find out.
What participation involves
- Procedures mentioned: CT scans
Only what the study's summary and detailed description on ClinicalTrials.gov say. Time periods may describe the whole study or a part of it — ask the study team what applies to you.
Show the study's own words
- "Perioperative, image-based sarcopenia using standard-of care preoperative chest computed tomography (CT) scans; Ib."
- Compensation
- Not stated
- Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
- Participants are monitored closely by the research team throughout the study.
- Some participants may receive access to an investigational treatment, which is still being studied.
- Your participation helps researchers learn whether this approach could help future patients.
About this study
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.
Compensation is read from the study's own description and may be missing — always confirm with the study team.
Eligibility
Official eligibility criteria
Inclusion Criteria: * 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 Exclusion Criteria: * 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)
Study sites (16)
CA
- University of California · Davis, CA 95616Lisa Brown, MD · Study contact · 916-734-3861 · lmbrown@ucdavis.eduLisa Brown, MD · Principal investigatorMore trials in Davis
- City of Hope Medical Center · Duarte, CA 91010Dan Raz · Study contact · 626-471-7100 · draz@coh.orgDan Raz · Principal investigatorMore trials in Duarte
- City of Hope at Irvine Lennar · Irvine, CA 92618More trials in Irvine
- Standard University · Stanford, CA 94305Natalie Lui, MD · Study contact · 415-378-1406 · natalielui@standford.eduNatalie Lui, MD · Principal investigatorMore trials in Stanford
- City of Hope at Upland · Upland, CA 91786More trials in Upland
CT
- Yale New Haven Medical Center · New Haven, CT 06510Justin Blasberg, MD · Study contact · 646-251-2670 · justin.blasberg@yale.eduJustin Blasberg, MD · Principal investigatorMore trials in New Haven
FL
- Moffitt Cancer Center · Tampa, FL 33612Eric Toloza, MD, PhD · Study contact · 813-745-7282 · eric.toloza@moffitt.orgEric Toloza, MD, PhD · Principal investigatorMore trials in Tampa
GA
- City of Hope at Georgia - Atlanta · Newnan, GA 30265Eldaif Shady, MD · Study contact · 404-252-9063 · seldaif@coh.orgMore trials in Newnan
IL
- Northwestern University · Evanston, IL 60208Samuel Kim, MD · Study contact · 312-694-6469 · samuel.kim2@nm.orgSamuel Kim, MD · Principal investigatorMore trials in Evanston
MA
- Massachusetts General Hospital (MGH) / Harvard · Boston, MA 02114Chi-Fu J. Yang, MD · Study contact · 617-726-6826 · cjyang@mgh.harvard.eduChi-Fu J. Yang, MD · Principal investigatorMore trials in Boston
- Lahey Hospital & Medical Center · Burlington, MA 01805Elliot Servais, MD · Study contact · 781-744-3170 · Elliot.Servais@lahey.orgMore trials in Burlington
MS
- University of Mississippi Medical Center · Jackson, MS 39216Jacob Moremen, MD · Study contact · 601-984-5170 · jmoremen@umc.eduJacob Moremen, MD · Principal investigatorMore trials in Jackson
NC
- Duke University · Durham, NC 27710Betty Tong, MD · Study contact · 919-613-4690 · betty.tong@duke.eduBetty Tong, MD · Principal investigatorMore trials in Durham
OH
- Ohio State University · Columbus, OH 43210Peter Kneuertz, MD · Study contact · 614-293-9059 · peter.kneuertz@osumc.eduPeter Kneuertz, MD · Principal investigatorMore trials in Columbus
TN
- Baptist Clinical Research Institute · Memphis, TN 38120Jane Zhao, MD · Study contact · 901-226-1366 · Jane.Zhao@bmhcc.orgJane Zhao, MD · Principal investigatorMore trials in Memphis
TX
- MD Anderson Cancer Center · Houston, TX 77030Mara Antonoff, MD · Study contact · 612-964-6469 · mbantonoff@mdanderson.orgMara Antonoff, MD · Principal investigatorMore trials in Houston