TENS for acute pain after VATS surgery
Official title: Effects of Transcutaneous Electrical Nerve Stimulation on Acute Postoperative Pain, Sleep Quality, and Quality of Life in Patients Undergoing Video-Assisted Thoracoscopic Surgery: A Randomized, Double-Blind, Sham-Controlled Study
Run by Fooyin University · NCT07732764 · Data updated 2026-11-12
A randomized, sham-controlled test will see if Transcutaneous Electrical Nerve Stimulation helps with acute pain after VATS surgery in adults and older teens.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 15 Years to 85 Years |
| Sex | All |
| Enrollment | 90 (estimated) |
| Sponsor | Fooyin University Academic / other |
| Locations | 1 site (Kaohsiung City, Kaohsiung City) |
| Status | Recruiting |
| Started | August 28, 2025 |
| Main results expected | October 2026 |
| Study ends | October 2026 |
| Registry record updated | July 29, 2026 |
| Trial ID | NCT07732764 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are 15 to 85 years old undergoing VATS who can read/write Chinese and can consent and comply with study procedures.
✕Probably not a fit
Patients who have a history of bleeding disorders, cardiac conditions, or are undergoing emergency or bilateral VATS may not benefit, and some may not respond to TENS.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized, double-blind, sham-controlled study tests whether active TENS applied after VATS can reduce acute postoperative pain, improve sleep quality, and enhance quality of life. Participants receive active or sham TENS for 30 minutes twice daily over three days, starting 24 hours post-surgery. Pain, sleep, and quality of life are measured at predefined time points to determine the effectiveness of TENS as an adjunctive pain-management option after thoracic surgery. The trial is conducted at Yuan's General Hospital with Fooyin University as lead sponsor.
Why it matters
Potential benefit: If successful, participants may experience less pain after VATS and better sleep and daily living during recovery.
How similar studies have gone: Prior studies with TENS for postoperative pain have shown mixed but promising results in various surgical settings.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria * Aged 15 to 85 years. * Participants younger than 18 years of age must have written informed consent provided by a parent or legal guardian. * Able to communicate and read/write in Chinese. * Scheduled to undergo video-assisted thoracoscopic surgery (VATS) as determined by the treating physician. * Have stable vital signs. * Willing to participate in the study and able to complete all study procedures. Exclusion Criteria * History of a bleeding disorder. * Patients undergoing emergency surgery. * Patients undergoing bilateral video-assisted thoracoscopic surgery (VATS). * History of cardiac disease, including cardiac arrhythmia or implantation of a cardiac pacemaker. * Known allergy or hypersensitivity to TENS electrodes or adhesive pads. * Cognitive impairment or inability to comply with the study procedures
Where it's running
-
Yuan's General Hospital
Kaohsiung City, Kaohsiung City, Taiwan Recruiting
Study contacts
- Principal investigator: Jia-Xin Lin, Np — Fooyin University
- Study coordinator: Jia-Xin Lin, Np
- Email: candy640930@gmail.com
- Phone: +886972091276
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
CYT-1010 in healthy volunteers and after third molar extraction
This trial tests CYT-1010, at single rising doses, for safety and tolerability in healthy adults and in people experiencing pain after removing wisdom teeth.
-
Pharmacogenetics of Tramadol Pain Control in Postoperative Care
This study tests whether CYP2D6 genetic differences affect how well tramadol works and its side effects in people recovering from surgery who all receive the same tramadol pump.
-
Visual Analog Scale–Guided Multimodal Pain Plan After Posterior Rib Remodeling
This study tests a pain management plan guided by a 0–10 pain score to see if it keeps postoperative pain low after posterior rib remodeling with osteosynthesis.
-
Sodium Oxybate to Improve Sleep After Thoracic Surgery
In adults having elective thoracoscopic surgery, this study tests whether giving sodium oxybate during operation improves sleep quality after surgery compared with a placebo.
-
A new treatment model for elderly lung cancer patients
This trial tests a comprehensive, integrated care approach for older adults with lung cancer to improve perioperative management and outcomes.
-
Topical lavender oil to help recovery after lung resection
This study tests whether applying lavender essential oil to the skin around the surgical wound for three days after lung surgery can improve recovery and reduce pain.
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.