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Not yet recruitingNCT07443540Updated Mar 2, 2026

The Effect of Acupuncture on Pulmonary Function Recovery Following Lung Resection

An interventional study of Acupuncture Therapy and Incentive Spirometry (Standard Rehabilitation) in Lung Nodules, sponsored by Chung Shan Medical University. Not yet recruiting. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-03-02.

Sponsored by Chung Shan Medical University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
56
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
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Study summary

Background and Purpose:

Lung resection surgery is the standard treatment for early-stage lung adenocarcinoma, but it often leads to reduced lung volume and postoperative pain, which can hinder pulmonary recovery. While standard rehabilitation includes breathing exercises (incentive spirometry) and pain management, additional strategies are needed to enhance recovery. Acupuncture has shown benefits in managing respiratory diseases like COPD and reducing surgical pain, but its specific effectiveness in rehabilitation after lung resection has not yet been established. This study aims to evaluate whether adding acupuncture to standard postoperative care can further improve lung function and recovery.

Study Design and Methods:

This is a randomized controlled clinical trial. Participants who have undergone lung resection will be assigned to one of two groups:

Control Group: Receives standard rehabilitation (lung volume training with incentive spirometry).

Intervention Group: Receives standard rehabilitation plus acupuncture therapy.

Evaluation:

One week after surgery, researchers will perform pulmonary function tests on all participants. The study will compare the two groups primarily based on improvements in lung function. Secondary outcomes, including pain levels and quality of life, will also be assessed to determine the overall benefit and safety of integrating acupuncture into postoperative recovery.

Read the detailed description

Lung resection surgery is the standard diagnostic and therapeutic approach for patients with early-stage lung adenocarcinoma. However, removal of part of the lung inevitably leads to a reduction in lung volume. In addition, postoperative pain often limits respiratory movement, resulting in impaired pulmonary function recovery. Therefore, rehabilitation strategies are essential to help maintain and restore cardiopulmonary capacity following surgery. According to current clinical guidelines, the most commonly recommended rehabilitation methods include structured cardiopulmonary training and adequate perioperative analgesia. Other supportive interventions, such as physical therapy and alternative exercise programs, have also been explored in recent clinical studies, with varying levels of effectiveness. Given the steadily increasing number of patients undergoing lung resection each year, the development and evaluation of additional therapeutic strategies to enhance postoperative pulmonary rehabilitation are of growing importance.

Acupuncture has been widely applied in the management of respiratory diseases and in perioperative pain control. Evidence from clinical studies supports its therapeutic effect in conditions such as asthma and chronic obstructive pulmonary disease (COPD). In patients with COPD, acupuncture has been shown to improve pulmonary function and quality of life. Furthermore, research has demonstrated that acupuncture can play a role in reducing postoperative pain and enhancing recovery. Despite these findings, a review of the literature indicates that no studies have yet specifically evaluated the efficacy of acupuncture in postoperative rehabilitation among patients who have undergone lung resection. Considering that lung cancer has been included in integrative oncology outpatient programs in traditional Chinese medicine, the potential role of acupuncture as an adjunct to rehabilitation after lung resection warrants systematic investigation.

This study is designed as a randomized controlled clinical trial. Patients in the control group will receive the current standard rehabilitation program, which consists of lung volume training with incentive spirometry following lung resection surgery. Patients in the intervention group will receive the same rehabilitation protocol with the addition of acupuncture therapy. Pulmonary function tests will be conducted one week after surgery in both groups to assess and compare postoperative outcomes. The primary endpoint will be the improvement of lung function parameters, while secondary outcomes will include pain levels, patient-reported quality of life, and tolerability of the intervention.

Through this design, the study aims to provide high-quality clinical evidence regarding the effectiveness of acupuncture in enhancing postoperative pulmonary rehabilitation after lung resection. The findings are expected to contribute to the development of integrative treatment strategies, offering patients improved recovery pathways that combine evidence-based conventional methods with traditional therapies.

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Conditions studied

  • Lung Nodules

Keywords

  • Lung nodules
  • acupuncture
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In context

Lead sponsor

Chung Shan Medical University is the lead sponsor of 124 studies on the registry; 26 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

- Patients aged between 18 and 65 years.

Diagnosed with a single pulmonary lesion (e.g., solitary pulmonary nodule or adenocarcinoma in situ).

Scheduled to undergo elective wedge resection for the lung lesion.

Exclusion criteria

Exclusion Criteria:

  • History of prior lung resection.

Medical history of asthma or pulmonary tuberculosis.

History of pneumothorax prior to the current surgery.

Expectation to receive rehabilitation therapies other than the standard protocol-defined incentive spirometry during the study period.

Presence of other major systemic diseases (e.g., severe cardiovascular, renal, or hepatic impairment) that, in the investigator's opinion, render the patient unsuitable for trial participation.

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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Single group
Masking
Single (Outcomes assessor)
Enrollment
56 participants (estimated)

Study arms

  • Experimental
    Acupuncture plus Standard Rehabilitation

    Participants in this group will receive acupuncture therapy in addition to the standard postoperative rehabilitation program. Standard rehabilitation includes lung volume training with incentive spirometry. Acupuncture sessions will be administered following lung resection surgery.

    Procedure: Acupuncture Therapy · Device: Incentive Spirometry (Standard Rehabilitation)

  • Active comparator
    Standard Rehabilitation Alone

    Participants in this group will receive the current standard rehabilitation program, consisting of lung volume training with incentive spirometry following lung resection surgery. No acupuncture therapy will be administered.

    Device: Incentive Spirometry (Standard Rehabilitation)

Interventions

  • ProcedureAcupuncture Therapy

    Acupuncture will be administered by certified practitioners.

  • DeviceIncentive Spirometry (Standard Rehabilitation)

    Postoperative lung volume training using an incentive spirometer. Participants are instructed to perform deep breathing exercises multiple times a day as per current clinical guidelines for lung resection recovery.

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What researchers measure

Primary outcomes

  1. Change from Baseline in Forced Vital Capacity (FVC)

    The change in Forced Vital Capacity (FVC), measured in liters, from the preoperative baseline to 1 week after surgery.

    Time frame: Baseline (pre-surgery) and 1 week after surgery.

  2. Change from Baseline in Forced Expiratory Volume in 1 second (FEV1)

    The change in FEV1, measured in liters, from the preoperative baseline to 1 week after surgery.

    Time frame: Baseline (pre-surgery) and 1 week after surgery.

  3. Change from Baseline in Diffusing Capacity of the Lungs for Carbon Monoxide (DLCo)

    The change in DLCo (measured in mL/min/mmHg) from the preoperative baseline to 1 week after surgery, to assess the gas exchange efficiency of the lungs.

    Time frame: Baseline (pre-surgery) and 1 week after surgery.

Secondary outcomes

  1. Postoperative Dyspnea Severity (Borg Scale)

    Assessed using the Modified Borg Scale to evaluate the severity of shortness of breath. The scale ranges from 0 (no breathlessness at all) to 10 (maximal breathlessness).

    Time frame: 1 week after surgery

  2. Postoperative Pain Intensity (Numerical Rating Scale, NRS)

    Assessed using the Numerical Rating Scale (NRS) for pain, where 0 indicates no pain and 10 indicates the worst possible pain.

    Time frame: Daily from postoperative day 1 through day 7

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: No — To protect the privacy of study participants and maintain data confidentiality in accordance with institutional review board (IRB) policies, there is no plan to share individual participant data with external researchers.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 2, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07443540
Lead sponsor
Chung Shan Medical University
Responsible party
Sponsor
First posted
Mar 2, 2026
Start date
Apr 1, 2026 (estimated)
Primary completion
Dec 30, 2026 (estimated)
Completion
Jan 30, 2027 (estimated)
Last update
Mar 2, 2026

Study contacts

KUEN-WEI LIN, master
Contact
raymond22432596@gmail.com
+886918432596

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

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