deltatrials
Recruiting INTERVENTIONAL NCT06026111

Preliminary Efficacy of Different Exercise Training During Immunotherapy in Patients With Lung Cancer: The ENHANCE Trial (ENHANCE)

Sponsor: Dana-Farber Cancer Institute

Conditions Lung Cancer
Updated 7 times since 2023 Last updated: Apr 9, 2026 Started: Feb 1, 2024 Primary completion: Dec 31, 2026 Completion: Dec 31, 2027
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

Listed as NCT06026111, this observational or N/A phase trial focuses on Lung Cancer and remains actively recruiting participants. Sponsored by Dana-Farber Cancer Institute, it has been updated 7 times since 2024, reflecting limited change activity. This study contributes to the evolving evidence base for cancer treatment protocols.

Study Description(click to expand)

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.

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.

Status Flow

~Oct 2023 – ~Mar 2024 · 5 months · monthly snapshotNot Yet Recruiting~Mar 2024 – ~Jul 2024 · 4 months · monthly snapshotRecruiting~Jul 2024 – ~Sep 2024 · 2 months · monthly snapshot~Sep 2024 – ~Feb 2025 · 5 months · monthly snapshotRecruiting~Feb 2025 – ~Feb 2026 · 12 months · monthly snapshotRecruiting~Feb 2026 – ~Apr 2026 · 2 months · monthly snapshotApr 16, 2026 – present · 4 months · daily APIRecruiting

Change History

7 versions recorded
  1. Apr 16, 2026 — Present [daily]

    Recruiting

    Phase: NANone

  2. Feb 2026 — Apr 2026 [monthly]

    Recruiting NA

  3. Feb 2025 — Feb 2026 [monthly]

    Recruiting NA

  4. Sep 2024 — Feb 2025 [monthly]

    Recruiting NA

  5. Jul 2024 — Sep 2024 [monthly]

    Recruiting NA

Show 2 earlier versions
  1. Mar 2024 — Jul 2024 [monthly]

    Recruiting NA

    Status: Not Yet RecruitingRecruiting

  2. Oct 2023 — Mar 2024 [monthly]

    Not Yet Recruiting NA

    First recorded

Eligibility 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:

Contact Information

Sponsor contact:
  • Dana-Farber Cancer Institute
  • National Cancer Institute (NCI)
Data source: ClinicalTrials.gov

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations