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NCT06008977Active, not recruiting

Exercise to Boost Response to Checkpoint Blockade Immunotherapy

Source: ClinicalTrials.gov · Last updated 25 Mar 2026

Brief summary (registry, in English)

The purpose of this pilot study will be to provide i) information on feasibility implementing an exercise intervention trial among patients with cutaneous cancers, including melanoma, squamous cell carcinoma (cuSCC), and Merkel cell carcinoma, scheduled to receive checkpoint blockade immunotherapy, and ii) preliminary data on the impact of a day-of-therapy exercise intervention.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
12 (actual)
First submitted
6 Jun 2023
Start date
3 Jun 2024
Primary completion date
7 Aug 2025
Lead sponsor
AdventHealth Translational Research Institute
Diseases
Melanoma
NCT number
NCT06008977

What you commit to

  • Study type: Interventional
  • Participants enrolled: 12
  • From 3 Jun 2024 to the primary completion date, 7 Aug 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Presence of medical conditions, such as severe cardiovascular disease for which exercise may be contraindicated. Participants may be referred to their medical team to obtain a cardiology approval.
  • Currently has a chronic, contagious, infectious disease, such as active tuberculosis, active Hepatitis B or C, HIV, or COVID-19, per self-report.
  • Presence of any condition that, in the opinion of the Investigator, compromises participant safety or data integrity or the participant's ability to complete the study.

Other

  • Presence of major postoperative complications for which an exercise intervention may be contraindicated.
  • Currently pregnant, lactating or planning to become pregnant (positive result on urine pregnancy testing).

Who the study is looking for

  • Males and females ≥18 years of age.
  • Able to read and speak English fluently.
  • Reported ability to complete 20-30 minutes moderate exercise per positive response to, "Can you currently walk unaided for six minutes or more?"
  • Scheduled for first-time checkpoint blockade immunotherapy with avelumab, cemiplimab, ipilimumab, nivolumab, or pembrolizumab in the absence of other therapies (e.g. targeted therapy) with the following diagnosis:
    • Adjuvant setting: cutaneous melanoma.
    • Neoadjuvant setting: cutaneous melanoma, cuSCC, or Merkel cell carcinoma.
  • States willingness to follow protocol as described, including the prescribed exercise level and completing any forms needed throughout the study.
  • Voluntarily signed and dated an informed consent form, approved by an Institutional Review Board/Independent Ethics Committee, and provided Health Insurance Portability and Accountability Act authorization (HIPAA) or other privacy authorization prior to any participation in study.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
AdventHealth Translational Research Institute
Coordinator of this site? Confirm its status
OrlandoUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.