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临床试验/NCT07120932
NCT07120932已完成不适用

Effects of Emotional Freedom Techniques (EFT) on Pain, Cardiac Anxiety and Sleep Quality in Patients Undergoing Coronary Artery Bypass Graft Surgery: A Randomized Controlled Trial

Hatice Balcı1 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2025年6月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
66
试验地点
1
主要终点
The Effect of Emotional Freedom Techniques (EFT) on Pain Levels in Patients Undergoing Coronary Artery Bypass Graft Surgery

研究概览

简要总结

Objective: To determine the effect of Emotional Freedom Techniques (EFT) on pain, cardiac anxiety and sleep quality in patients undergoing Coronary Artery Bypass Graft (CABG) surgery.

Materials and Methods: The study will be conducted between 2025 and 2026 as a pretest-posttest, parallel design (1:1) randomized controlled trial. The study population will consist of patients undergoing coronary artery bypass grafting (CABG) at the Kütahya City Hospital Cardiovascular Surgery Department. The sample size was determined to be 66 patients, with 33 patients each in the experimental and control groups.

Measurement tools include a Personal Information Form, Visual Analog Scale (VAS), Cardiac Anxiety Scale, and Richard Campbell Sleep Scale. Data will be collected through one-on-one patient interviews.

The researcher has successfully completed a 3.5-hour EFT training program at the Boğaziçi Education Institute. EFT will be administered to the patients by the researcher.

Patients undergoing coronary artery bypass graft surgery at the Cardiovascular Surgery Clinic who volunteer to participate in the study and meet the inclusion criteria will complete the Informed Consent Form, Personal Information Form, Visual Analogue Scale (VAS), Cardiac Anxiety Scale, and Richard-Campbell Sleep Scale. Patients will then be assigned to the experimental or control groups by a person other than the researcher based on the randomization list. Patients in the experimental group will receive EFT in addition to standard cardiovascular surgery clinic procedures, while patients in the control group will receive standard cardiovascular surgery clinic procedures. Data analysis will be conducted using SPSS. The study will be conducted in accordance with the principles of the Declaration of Helsinki.

Findings: The findings of the research will be written after the data to be obtained after the implementation of the research and data collection will be analyzed in the SPSS program.

Conclusion: The results of the research will be written by determining the findings after analyzing the data to be obtained after the implementation of the research and data collection in the SPSS program.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients who are:
  • •18 years of age or older,
  • •3 days postoperatively after coronary artery bypass graft surgery,
  • •literate,
  • •conscious and able to communicate will be included.

排除标准

  • •Patients with speech, hearing, or visual impairments
  • •Patients who do not believe in the effectiveness of the procedure due to prejudice will not be included.

研究组 & 干预措施

Emotional Freedom Techniques (EFT)

Experimental

Effects of Emotional Freedom Techniques (EFT)

干预措施: Effects of Emotional Freedom Techniques (EFT) (Behavioral)

Control arm

No Intervention

Standard care will continue without intervention.

结局指标

主要结局

The Effect of Emotional Freedom Techniques (EFT) on Pain Levels in Patients Undergoing Coronary Artery Bypass Graft Surgery

时间窗: The application, which will last 1 week for each patient, is planned for 15.09.2025-15.12.2025 dates.

The effect of EFT on the patient's pain level will be measured. The Effect of Emotional Freedom Techniques (EFT) on Pain Levels in Patients Undergoing Coronary Artery Bypass Graft Surgery. The measurement tool is a Visual Analog Scale (VAS).

次要结局

  • The Effect of Emotional Freedom Techniques (EFT) on Cardiac Anxiety Levels in Patients Undergoing Coronary Artery Bypass Graft Surgery(The application, which will last 1 week for each patient, is planned for 15.09.2025-15.12.2025 dates.)

研究者

发起方
Hatice Balcı
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Hatice Balcı

PhD

KTO Karatay University

研究点 (1)

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