RecruitingNot ApplicableNCT06513663

Exercise as Maintenance Therapy in Advanced Lung Cancer


Sponsor

Indiana University

Enrollment

100 participants

Start Date

Oct 15, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to examine how a multimodality (having or using a variety of methods to do something) exercise intervention may improve survival, function, and quality of life in participants with advanced lung cancer.


Eligibility

Min Age: 18 Years

Inclusion Criteria8

  • Age ≥ 18 years
  • Known diagnosis of locally advanced (stage III) or metastatic NSCLC
  • Patient is currently receiving maintenance immunotherapy for at least 1 month and planned for at least 3 additional months of therapy
  • Patients receiving maintenance therapy refers to patients with stable disease or partial response to therapy, including patients who have had a history of disease progression but are currently stable or responding to a different therapy
  • Patients previously receiving chemotherapy are eligible as long as at least one month has elapsed since completing chemotherapy. Those currently receiving chemotherapy are not eligible.
  • Patient is willing and able to participate in a supervised home-based exercise program as determined by the MOVE program
  • a.Participants must have internet access and equipment to participate in virtual exercise
  • ECOG performance status of 0-2

Exclusion Criteria7

  • Already meeting exercise guidelines and participating in at least 150 minutes of moderate or vigorous exercise per IPAQ
  • Unable to participate in the supervised home-based exercise program as determined by the MOVE program
  • Medical co-morbidities that preclude patient from participating in supervised exercise, including but not limited to:
  • Advanced heart failure
  • Advanced respiratory disease requiring home oxygen use
  • Uncontrolled psychiatric disorders
  • History of fragility fracture

Interventions

BEHAVIORALExercise Intervention

Eligible and consented participants randomized to the exercise arm will work with an exercise trainer three times weekly for 12 weeks. Training sessions will be delivered virtually using HIPPA Complaint IU Health Zoom. These sessions will last 60 minutes and include cardiovascular exercise, resistance training, and balance or stretching exercise. The participants will be able to use any equipment they already have at home but will be provided a heart monitor and a set of resistance bands. All sessions will have a moderate-intensity training goal, defined as 40-80% of heart rate reserve (HRR). Cardiovascular exercise will include any at-home equipment available to the participants or follow a Tabata-style program. Resistance training will include a full body workout, emphasizing all major muscle groups. Trainers will progress or regress intensity levels based on the participant's rate of perceived exertion (RPE), heart rate, and individual response during each session.


Locations(3)

Indiana University Health Methodist Hospital

Indianapolis, Indiana, United States

Indiana University Melvin & Bren Simon Comprehensive Cancer Center

Indianapolis, Indiana, United States

Sidney and Lois Eskenazi Hospital

Indianapolis, Indiana, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06513663


Related Trials