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Pain, AcuteNCT07411417

Combined Acupressure Effects on Post-Thoracotomy Pain and Lung Volume

A study testing Acupressure group in people with Pain, Acute and Breathing, Mouth, run by Özgül Aydemir at 1 site in Turkey (Türkiye).

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Pain is a subjective, sensory and emotionally unpleasant experience resulting from real or hidden injuries in tissues. The pain experience is a subjective and unique experience in physiological and psychological terms and is the first negative sensory experience of the patient after the surgical procedure. Read more about this study

Who is it for?
Any age
What is being tested?
Acupressure group
Could I receive a placebo?
No, everyone receives an active treatment
How many people
80 participants
Where
1 siteTurkey (Türkiye)
Study dates
6 Jan 2025to 6 Jan 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • Underwent thoracotomy
  • Undergoing thoracic surgery for the first time
  • Classified as ASA (American Society of Anesthesiology) physical status I, II and III
  • Presence of a drain upon admission to the intensive care unit
  • Conscious, oriented, and cooperative
  • Provided verbal and written informed consent after receiving information about the study

Who cannot join

  • Intubated
  • Persistent anxiety before the surgery
  • Diagnosed with panic disorder
  • Chemotherapy within the last 6 months
  • Diagnosed psychiatric illness or mental health problems
  • Presence of edema
Show all 10Show fewer
  • Intraoperative or postoperative complications
  • Non-Turkish speaking, or presence of hearing or visual impairment
  • Body mass index (BMI) greater than 30
  • Participation in another clinical trial during the study period

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Özgül Aydemir, Doctor contact

+905435326567

ozgul6761@gmail.com

Öykü Kara, Specialist contact

+905546669614

oyku.kara@iuc.edu.tr

Turkey (Türkiye)1 site, 1 recruiting
  • Özgül Aydemir

    Istanbul, 34067

    Özgül Aydemir, Doctor, +905435326567, ozgul6761@gmail.com

    Öykü Kara, Specialist, +905546669614, oyku.kara@iuc.edu.tr

    Recruiting

Other trials in Turkey (Türkiye)

About this study

Official title: The Effects of Acupressure Combination on Post-Thoracotomy Pain and Lung Volume During Rest, Breathing-Coughing Exercises: A Randomized Controlled Study

Pain is a subjective, sensory and emotionally unpleasant experience resulting from real or hidden injuries in tissues. The pain experience is a subjective and unique experience in physiological and psychological terms and is the first negative sensory experience of the patient after the surgical procedure. Thoracotomy is an invasive surgical incision that causes severe postoperative pain due to the negative effect on the ribs, muscles and peripheral nerves. During thoracic surgery, anatomical lung resection is performed through posterolateral thoracotomy. Surgical incision during thoracotomy surgery is the most severe cause of postoperative pain. Epidural analgesia, peripheral nerve block and systematic treatment methods are used in post-thoracotomy pain management. Opioid use is frequently preferred in post-thoracotomy pain management. Although thoracotomy pain can mostly be controlled with opioid analgesics, excessive use of opioids may lead to respiratory suppression, constipation, suppression of cough, nausea, vomiting and many other possible side effects. Ineffective postoperative pain management may lead to postoperative complications such as increased cardiac workload, prolonged pulmonary rehabilitation and delayed wound healing. The use of holistic non-drug pain relief methods is vital in reducing the need for opioid analgesics and the risk of possible side effects in early postoperative pain management.

Read the detailed description

Many non-drug applications such as music therapy, transcutaneous electrical nerve stimulation, cryotherapy, acupuncture, electroacupuncture are used in pain management after thoracic surgery and to reduce analgesic use. Acupuncture is an application that provides the balance of energy flow (Qi) on meridians with thin needles placed at certain points of the body, which has been widely applied in China for more than 4000 years. Factors such as trauma and surgical incision disrupt the energy flow between meridians and cause problems in organ groups where meridians are effective. Acupuncture is accepted as an application that helps to balance this energy flow. Acupressure application, which is included in nursing practices, is a holistic non-pharmaceutical application based on acupuncture. Acupressure is a holistic treatment method that includes manual and noninvasive methods that provide stimulation to acupuncture points with pressure instead of needle stimulation. The point where acupressure will be applied is selected among the acupuncture points on the relevant meridian according to the problem existing in the individual. In acupressure application, pressure can be applied to a single point or more than one point consecutively.In acupressure application, it is reported that pressure can be applied to a single point, as well as stimulating multiple points consecutively will increase the desired effect. As the preferred acupuncture key points on the meridians, points on the hand, finger, wrist, palm, elbow, knee, and feet are often preferred. Acupressure tactilely reduces the sensation of pain by stimulating Aβ nerve fibres; increases the pain threshold by supporting the release of endogenous opioids; regulates the transmission of pain signals by secreting serotonin and norepinephrine, which are neurotransmitters responsible for the regulation of pain. In a randomised controlled study, the efficacy of acupressure in the treatment of postoperative pain in patients undergoing thoracoscopic surgery was examined. The participants in the experimental group were acupressured three times a day for two days at LI11, LU7, LU9, LU5, LU1, LU2, TE5, TE6, PC4, PC6 and LI4 acupressure points. In the control group, routine treatment of the clinic was applied and acupressure was not applied. After acupressure application, the pain score of the experimental group was found to be lower compared to the control group (p < 0.001). Similarly, it is reported in the literature that the use of acupressure is one of the best options for the relief of postoperative pain. It is also reported in the literature that acupressure can effectively improve lung function, dyspnoea and quality of life of patients with pneumonia.

Non-drug applications planned for the expected pain in the early postthoracotomy period are important in terms of reducing respiratory complications, improving the quality of pain management and supporting patients. When the literature is examined, there is no study examining the effect of acupressure on pain and lung volume during deep breathing and cough exercises, which have an important role in maintaining and improving lung volume after thoracotomy.

Being tested
Acupressure group
Keywords
Thoracotomy after Pain, Acupressure, Pain, Lung Volume
Medical subject headings
Acute Pain, Mouth Breathing, Cough, Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Acupressure groupOther

    A series of acupressure applications

Study groups in NCT07411417
Study groupRoleWhat they receive
Acupressure groupExperimentalPatients meeting the research criteria were included in the experimental group according to the randomisation table. The acupressure combination will be applied to the LI11, LU7, LU9, LU5, LU1, LU2, TE5, TE6,PC4, PC6 and LI4 points 2, 6 and 24 hours after surgery. Applications will last 1 minute for each point. Applications will last 1 minute for each point. Patients in this group will continue to receive routine clinical treatment and care. The patients' pain level during rest, breathing, coughing and mobilisation before surgery and 2, 6 and 24 hours after surgery, blood pressure, respiratory rate, respiratory count, SpO2 values, and lung volume before surgery and 24 hours after surgery will be measured and recorded using triflow. Additionally, the individuals' breathing and coughing exercise status will be assessed within the first 24 hours after surgery. These stages will also be carried out in a similar manner in the control group without any intervention.
Receives: Other: Acupressure group
Control groupNo interventionPatients meeting the study criteria were included in the control group according to the randomisation table. Patients in this group will continue to receive routine clinical treatment and care. The patients' pain level during rest, breathing, coughing and mobilisation before surgery and 2, 6 and 24 hours after surgery, blood pressure, respiratory rate, respiratory count, SpO2 values, and lung volume before surgery and 24 hours after surgery will be measured and recorded using triflow. Additionally, individuals' breathing and coughing exercise status will be assessed within the first 24 hours after surgery.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pain after thoracotomy

    Pain after thoracotomy

    Measured: The patient's visual analogue scale pain score (VAS) at 2, 6, and 24 hours post-surgery,

Secondary outcomes (1)
  1. Pain during rest

    Pain during rest

    Measured: The patient's visual analogue scale pain score (VAS) at 2, 6, and 24 hours post-surgery

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 Feb 2026
  2. Study start6 Jan 2025
  3. Primary completion6 Jun 2026 (estimated)
  4. Study completion6 Jan 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Parallel Assignment Randomised controlled experimental
Masking
Single blind
Who is masked
Care provider
Enrolment
80 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07411417
Sponsor's protocol ID
E-95961207-202.3.02-5421
Status last verified
Feb 2026
First submitted
31 Mar 2025
Last updated
13 Feb 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Acupressure group in people with Pain, Acute and Breathing, Mouth, run by Özgül Aydemir at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 13 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Özgül Aydemir, Doctor (+905435326567, ozgul6761@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Pain after thoracotomy (time frame: The patient's visual analogue scale pain score (VAS) at 2, 6, and 24 hours post-surgery,). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Feb 2026.

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