Back to Clinical Trials
N/ARecruiting

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

Sponsored by City of Hope Medical Center

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.

PRIMARY OBJECTIVE: I. To compare changes from baseline in objective patient functional capacity as measured by 6 minute walk test (6MWT) at day 30 post-discharge between the two comparators. SECONDARY OBJECTIVES: I. To compare the following outcomes between the two comparators: Ia. 6MWT at 60 and 180 days post discharge; Ib. Short Physical Performance Battery (SPPB) at 30, 60, and 180 days post-discharge; Ic. The following scores at 30, 60, and 180 days post-discharge: a) patient and family caregiver (FCG) reported self-efficacy; b) patient and FCG reported physical function; c) and patient and FCG quality of life (QOL); Id. Patient time at home and away from the hospital through 60 days post-discharge; Ie. Hospital readmissions rate and postoperative complications through 60 days post…

Where this study is enrolling (14)

Show all 14 locations
Who can participate

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)

Only the research team can confirm whether you qualify. The intake questionnaire is the best way to find out.

Completing a questionnaire on Clinably does not enroll you in a clinical trial or confirm your eligibility. Only the research team can determine whether you qualify to participate. These results are based on the information you provide and are intended to help you start a conversation with the research team.

Trial data sourced from ClinicalTrials.gov.