Using auricular acupressure to improve health before lung surgery
Official title: A Pilot Study of the Utility of Auricular Acupressure in Enhancing Prehabilitation Benefits in Candidates for Thoracic Surgery.
Run by University of Chicago · NCT06516198 · Data updated 2026-11-12
This study is testing whether auricular acupressure can help improve the health and well-being of people aged 50 and older who are getting ready for major lung surgery.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 50 Years and up |
| Sex | All |
| Enrollment | 40 (estimated) |
| Sponsor | University of Chicago Academic / other |
| Drugs / interventions | chemotherapy |
| Locations | 1 site (Chicago, Illinois) |
| Status | Recruiting |
| Started | July 21, 2025 |
| Main results expected | June 20, 2027 |
| Study ends | June 20, 2027 |
| Registry record updated | December 9, 2025 |
| Trial ID | NCT06516198 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are individuals aged 50 and older who are preparing for major lung surgery and can commit to a prehabilitation program.
✕Probably not a fit
Patients with allergies to Vaccaria seeds or medical conditions affecting the ear that prevent the use of auricular acupressure may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study explores the use of auricular acupressure as a complementary therapy to enhance prehabilitation for patients undergoing major lung surgery. By targeting specific points in the ear, the intervention aims to improve physical and mental health, potentially alleviating pain, anxiety, and fatigue. Participants will be individuals aged 50 and older who are scheduled for lung surgery and will engage in a prehabilitation program lasting at least two weeks. The study will assess the effectiveness of this approach in preparing patients for surgery.
Why it matters
Potential benefit: If successful, this approach could improve the overall health and recovery outcomes for patients undergoing lung surgery.
How similar studies have gone: Previous studies have shown that auricular acupressure can improve various health outcomes, suggesting potential success for this novel application in prehabilitation.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria * Being considered for major lung surgery * Surgery is not scheduled for at least 2 weeks * Age ≥ 50 years * Able to understand English at a 4th grade level * No known contraindications to prehabilitation (strength, endurance, balance exercises) * Able to provide informed consent for participation * Has an adult care partner who will be available and capable of placing seeds * Has access to smart phone for communication and image sharing * Underwent frailty screening (given any score) * Able to perform spirometry testing in clinic Exclusion Criteria: * Allergy to Vaccaria seeds * Medical condition affecting either ear preventing use of auricular acupressure such as eczema, frostbite, sunburn
Where it's running
-
University of Chicago
Chicago, Illinois, United States Recruiting
Study contacts
- Principal investigator: Maria Lucia Madariaga, MD — University of Chicago
- Study coordinator: Maria Lucia Madariaga, MD
- Email: mlmadariaga@bsd.uchicago.edu
- Phone: 7737022500
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Pre-incisional ropivacaine plus diprospan to relieve pain after VATS
This study tests whether injecting ropivacaine with diprospan before surgery can reduce postoperative pain for adults and children undergoing VATS lung surgery.
-
Personalized pain management after thoracic surgery
This study is testing a new way to manage pain after lung surgery to see if personalized plans can help patients feel better and use fewer opioids.
-
Force feedback in robotic lung resection: does gentler instrument touch help recovery?
This study tests whether using Force Feedback instruments during robotic lobectomy or segmentectomy leads to faster recovery and fewer complications for adults undergoing these procedures.
-
Infiltration with ropivacaine plus triamcinolone to relieve pain after VATS surgery
This study tests whether injecting ropivacaine with or without triamcinolone before incision can reduce pain after thoracoscopic lung surgery in adults.
-
Prehabilitation program for frail adults undergoing thoracic surgery
This study is testing a prehabilitation program for frail adults scheduled for thoracic surgery to see if it helps them get stronger and recover better after their operation.
-
Left-sided stellate ganglion block to lower post-surgery atrial fibrillation risk
This will test if giving an ultrasound-guided left stellate ganglion block with bupivacaine to adults having esophagectomy, pneumonectomy, or lobectomy lowers their chance of atrial fibrillation after surgery.
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.