Pilot Precision Exercise Program for Lung Cancer Care
Official title: PILOT for The Precision Exercise Regimen for Cancer Care (PERCC) Study
Run by University of Utah · NCT06945484 · Data updated 2026-11-12
This pilot will test whether a personalized, virtually supervised home exercise program delivered by telehealth can be implemented and helpful for people with stage II-III non-small cell lung cancer who are receiving chemotherapy or immunotherapy plus surgery.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 20 (estimated) |
| Sponsor | University of Utah Academic / other |
| Drugs / interventions | chemotherapy, immunotherapy, radiation |
| Locations | 2 sites (Galveston, Texas and 1 other locations) |
| Status | Recruiting |
| Started | November 21, 2025 |
| Main results expected | January 2027 |
| Study ends | December 2030 |
| Registry record updated | November 3, 2026 |
| Trial ID | NCT06945484 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (18+) with stage II or III non-small cell lung cancer who are starting neoadjuvant chemotherapy or immunotherapy and are scheduled for surgery, can communicate in English or Spanish, and agree to a telehealth-supervised exercise program.
✕Probably not a fit
Patients with BMI extremes (>40 or <17.5), medical or physical contraindications to exercise, active substance or severe mental health issues that prevent participation, those receiving single-modality treatment, or those unable to use telehealth are unlikely to benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This pilot tests the Precision Exercise Regimen for Cancer Care (PERCC), a virtually supervised, home-based program for patients with stage II–III non-small cell lung cancer receiving multimodal treatment. Participants begin exercise at least two weeks before their first neoadjuvant therapy and continue until about two months after surgery, with sessions delivered via telehealth. The program includes mobility, aerobic, and resistance exercises performed in varied postures and daily activities, with progression tailored to each participant. Feasibility outcomes focus on implementation, adherence, safety, and integration with routine care at the participating cancer centers.
Why it matters
Potential benefit: If successful, the program could help patients maintain function, reduce treatment-related decline, and speed recovery after surgery.
How similar studies have gone: Exercise interventions have shown fitness and recovery benefits in various cancer populations, but precision, virtually supervised regimens specifically for preoperative stage II–III NSCLC are relatively novel and supported mainly by small pilot data.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Ages 18 and older at time of diagnosis * Patient diagnosed with stage II and III non-small cell lung cancer (NSCLC) * Patient receives neoadjuvant therapy (defined as chemotherapy, radiation therapy immunotherapy, or any combination of these modalities) and surgery * Patient able to follow direction and complete questionnaires in English or Spanish * Patient agrees to complete the PERCC intervention Exclusion Criteria: * Morbidly obese (BMI \>40 kg/m2 ) or anorexic (BMI \<17.5 kg/m2 ) * Abnormalities on screening physical exam per study physicians or physical therapist to contraindicate participation in exercise program compliance * Alcohol or drug abuse, significant mental or emotional problems that would interfere with compliance (assessed by NCCN Distress Thermometer) * Patient scheduled to receive single modality cancer treatment (unimodal therapy), scheduled to begin treatment within 2 weeks of the pre-treatment clinic visit, or for whom treatment has already started
Where it's running
-
University of Texas Medical Branch at Galveston
Galveston, Texas, United States Recruiting -
Huntsman Cancer Institute
Salt Lake City, Utah, United States Recruiting
Study contacts
- Principal investigator: Thomas Varghese, MD, MS, MBA, FACS — Huntsman Cancer Institute
- Study coordinator: Thomas Varghese, MD, MS, MBA, FACS
- Email: thomas.varghese@hsc.utah.edu
- Phone: 801-581-5311
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Adaptive Chemotherapy for PD-L1 High Resectable NSCLC: A Chemo-PHREE Trial
This study tests cemiplimab in adults with resectable non-small cell lung cancer to see if surgery can be pursued without preceding chemotherapy for some patients.
-
Anti-CTLA-4 plus sintilimab and chemotherapy before surgery for resectable Stage II–III NSCLC
This trial will test whether adding an anti-CTLA-4 antibody (IBI310) to sintilimab plus chemotherapy before surgery helps people with PD-L1–negative, resectable Stage II–III non-small cell lung cancer.
-
BIO 300 with thoracic radiation for early-stage non-small cell lung cancer and interstitial lung disease
This trial will test whether adding BIO 300 to thoracic radiation lowers the chance of pneumonitis in people with stage I–II non-small cell lung cancer who also have interstitial lung disease.
-
Testing Repotrectinib in Elderly and Frail Patients with Advanced NSCLC
This study is testing a new cancer drug called repotrectinib to see if it helps older and frail patients with advanced lung cancer feel better and tolerate the treatment well.
-
Combining hormone therapy and immunotherapy for advanced lung cancer
This study is testing if combining hormone therapy with a type of immunotherapy can help older men with advanced lung cancer respond better to treatment.
-
Understanding the diagnosis and treatment of early and locally advanced non-small cell lung cancer
This study looks at how patients with early and locally advanced non-small cell lung cancer are diagnosed and treated after surgery or radiation to see how well different approaches work.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.