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Clinical Trial Summary

The purpose of this study is to examine the feasibility and effects of 12-week exercise training at different intensities among individuals with advanced lung cancer receiving immune checkpoint inhibitors. The names of the study interventions involved in this study are:


Clinical Trial Description

This single-center, two-armed, pilot randomized controlled research study will assess feasibility and compare immune activities, cardiorespiratory fitness, physical function, and immunotherapy-related adverse events, and patient-reported outcomes between three groups - high-intensity exercise, moderate-intensity exercise, and usual care. Participants in this study will be randomly assigned to one of three groups: - High-intensity interval training (HIIT) - Moderate-intensity continuous training (MICT) - Usual care (UC) The HIIT and the MICT groups will receive virtually supervised home-based exercise training three sessions per week for 12 weeks. The UC group will be asked not to change their baseline exercise behavior and will be offered to receive one of the exercise programs at the end of the initial 12 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06026111
Study type Interventional
Source Dana-Farber Cancer Institute
Contact Dong-Woo Kang, PhD
Phone 857-215-2229
Email Dong-Woo_Kang@dfci.harvard.edu
Status Recruiting
Phase N/A
Start date February 1, 2024
Completion date December 31, 2025

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