- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06839625
The Effect of Emotional FreedomTechnique on Postoperative Pain, Pain Belief and Anxiety in Coronary Artery Bypass Graft Planned Patients
May 7, 2026 updated by: Özge İşeri, Ondokuz Mayıs University
When the literature is examined, there is almost no application of EFT on surgical patients.
In a quasi-experimental study conducted by Kalroozi et al. (2022) with 70 women who underwent breast cancer surgery and received complementary treatment, the effect of EFT on sleep quality and happiness level was investigated.
Six sessions of EFT were applied to the control group.
A statistically significant difference was found between the intervention and control groups in sleep quality and happiness scores before and after the intervention.
In a randomised controlled study conducted by Menevşe et al. (2024) examining the effect of EFT applied to patients before laparoscopic cholecystectomy on surgical fear and anxiety, 56 patients were included in the control and 56 patients in the intervention group.
While routine care and treatment practices were applied to the control group, EFT was applied to the intervention group.
EFT application was continued for three rounds and approximately 25-30 minutes.
As a result of the study, it was found that EFT was useful in clinical practice in the preoperative period and reduced surgical anxiety and surgical fear.
In a quasi-experimental study involving 108 people in which the effects of EFT and music on anxiety and vital signs were examined before lumbar disc herniation surgery, it was found that both music and EFT reduced anxiety and regulated vital signs before surgery, and EFT was more effective than music in regulating anxiety and respiratory rate.
In previous studies, pain, pain belief and anxiety in surgical patients have not been examined together.
It is thought that the study will have a positive effect on the patient outcomes (anxiety, pain, pain belief) of patients undergoing CABG, thus increasing the holistic approach in the care of patients and having a positive effect on the quality of life of individuals.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
Cardiovascular diseases are among the most important causes of mortality and morbidity rates occurring in the world and in our country every year despite the developing technology and treatment methods (1).When the Death and Cause of Death statistics of the Turkish Statistical Institute for 2023 are examined, it is seen that the mortality rate due to circulatory system diseases is 33.4% (2).In the treatment of heart diseases, surgical treatment is frequently preferred in addition to medical treatment.
The most commonly used surgical method is open heart surgery (1).Coronary Artery Bypass Graft (CABG) surgery provides re-blooding, oxygenation and nutrition of the non-blooded heart tissue by using artery or vein between the aorta in cases of stenosis or occlusion in the structure of the coronary vessels.
CABG is a frequently used method in the world and in our country (3).
Regardless of the source of surgical intervention, it causes anxiety in patients.
When the literature is examined, it is seen that anxiety is experienced in the majority of surgical patients (4).
Fear of death and the unknown, complications that may develop after surgery, pain, loss of organ and independence are among the main causes of anxiety (4).
In a study in which anxiety levels of patients who will undergo open heart surgery were examined, preoperative anxiety level was found to be 55.80% (5).The vital importance of the heart increases the fear of death and forms the basis of anxiety in the preoperative and postoperative period (1).
In the review, it was found that there were descriptive studies on preoperative anxiety of CABG patients (6, 7, 8, 9), and intervention studies were mostly performed in the form of scent sniffing (10), acupressure (11) music therapy (12,13,14) education (13,15,16); emotional freedom technique was not used.
Study Type
Interventional
Enrollment (Actual)
66
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Atakum
-
Samsun, Atakum, Turkey (Türkiye)
- Ondokuz Mayıs Unıversity
-
-
İlkadım
-
Samsun, İlkadım, Turkey (Türkiye)
- Samsun Training and Research Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Over 18 years old
- No infections, sores in the touch areas
- No psychiatric medication
- No hearing and vision problems
- Stable vital parameters
Exclusion Criteria:
- Patients undergoing re-operation
- Postoperative complications (bleeding, delirium, arrhythmia, etc.)
- Reintubation after extubation
- Drug and stimulant users
- Sedated for more than 24 hours
- Patients unstable for more than 24 hours
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control
routine care
|
|
|
Experimental: Experimental group
Emotional freedom technique
|
EFT application
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
VAS scale
Time Frame: Pre-test before surgery; post-test 24-48 hours after surgery
|
Pain
|
Pre-test before surgery; post-test 24-48 hours after surgery
|
|
Pain Belief Scale
Time Frame: Pre-test before surgery; post-test 24-48 hours after surgery
|
Pain belief
|
Pre-test before surgery; post-test 24-48 hours after surgery
|
|
State Anxiety Scale
Time Frame: Pre-test before surgery; post-test 24-48 hours after surgery
|
Anxiety
|
Pre-test before surgery; post-test 24-48 hours after surgery
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 12, 2025
Primary Completion (Actual)
August 31, 2025
Study Completion (Actual)
January 30, 2026
Study Registration Dates
First Submitted
February 12, 2025
First Submitted That Met QC Criteria
February 17, 2025
First Posted (Actual)
February 21, 2025
Study Record Updates
Last Update Posted (Actual)
May 11, 2026
Last Update Submitted That Met QC Criteria
May 7, 2026
Last Verified
February 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- E-26521195-604.01-262284337
- Ondokuz Mayıs University (Other Identifier: Ondokuz Mayıs University)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
This is a master thesis.
sharing can be done at the end of the study
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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