Clinical trial Recruiting at 2 sites Interventional Ages 18 and up

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 typeInterventional
Ages18 Years and up
SexAll
Enrollment20 (estimated)
SponsorUniversity of Utah
Academic / other
Drugs / interventionschemotherapy, immunotherapy, radiation
Locations2 sites (Galveston, Texas and 1 other locations)
StatusRecruiting
StartedNovember 21, 2025
Main results expectedJanuary 2027
Study endsDecember 2030
Registry record updatedNovember 3, 2026
Trial IDNCT06945484 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.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.