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
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| AdventHealth Translational Research Institute Coordinator of this site? Confirm its status | Orlando | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.