RECRUITING

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

Description

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.

Conditions

Lung Carcinoma
Talk to us

Related Conditions:

Lung Carcinoma

Study Overview

On this page

Study Details

Study overview

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.

SR2204: a Randomized Phase III Trial of a Perioperative Physical Activity Intervention in Older Adults with Lung Cancer and Their Family Caregivers

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

Condition
Lung Carcinoma
Intervention / Treatment

-

Contacts and Locations

Davis

University of California, Davis, California, United States, 95616

Duarte

City of Hope Medical Center, Duarte, California, United States, 91010

Standford

Standard University, Standford, California, United States, 94305

Stanford

Standford University, Stanford, California, United States, 94305

New Haven

Yale New Haven Medical Center, New Haven, Connecticut, United States, 06510

Tampa

Moffitt Cancer Center, Tampa, Florida, United States, 33612

Evanston

Northwestern University, Evanston, Illinois, United States, 60208

Boston

Massachusetts General Hospital (MGH) / Harvard, Boston, Massachusetts, United States, 02114

Jackson

University of Mississippi Medical Center, Jackson, Mississippi, United States, 39216

Durham

Duke University, Durham, North Carolina, United States, 27710

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility 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
  • * 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)

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

City of Hope Medical Center,

Dan Raz, MD, PRINCIPAL_INVESTIGATOR, City of Hope Medical Center

Study Record Dates

2028-05-16