NCT07120932

Brief Summary

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.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
66

participants targeted

Target at P50-P75 for not_applicable

Timeline
2mo left

Started Apr 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress50%
Apr 2026Aug 2026

First Submitted

Initial submission to the registry

July 16, 2025

Completed
28 days until next milestone

First Posted

Study publicly available on registry

August 13, 2025

Completed
8 months until next milestone

Study Start

First participant enrolled

April 15, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 15, 2026

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 15, 2026

Expected
Last Updated

February 20, 2026

Status Verified

February 1, 2026

Enrollment Period

2 months

First QC Date

July 16, 2025

Last Update Submit

February 19, 2026

Conditions

Keywords

Coronary Artery Bypass Graft SurgeryEffects of Emotional Freedom Techniques (EFT)Pain ManagementAnxietySleep

Outcome Measures

Primary Outcomes (1)

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

    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).

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

Secondary Outcomes (1)

  • 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.

Other Outcomes (1)

  • The Effect of Emotional Freedom Techniques (EFT) on Sleep Quality 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.

Study Arms (2)

Emotional Freedom Techniques (EFT)

EXPERIMENTAL

Effects of Emotional Freedom Techniques (EFT)

Behavioral: Effects of Emotional Freedom Techniques (EFT)

Control arm

NO INTERVENTION

Standard care will continue without intervention.

Interventions

Effects of Emotional Freedom Techniques (EFT)

Emotional Freedom Techniques (EFT)

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

KTO Karatay University

Konya, Karatay, 42020, Turkey (Türkiye)

Location

MeSH Terms

Conditions

AgnosiaAnxiety Disorders

Condition Hierarchy (Ancestors)

Perceptual DisordersNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and SymptomsMental Disorders

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
PhD

Study Record Dates

First Submitted

July 16, 2025

First Posted

August 13, 2025

Study Start

April 15, 2026

Primary Completion

June 15, 2026

Study Completion (Estimated)

August 15, 2026

Last Updated

February 20, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be shared in accordance with personal data protection laws. However, if requested by the journal boards involved in an academic publication, data will be shared within ethical limits.

Locations