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CompletedNCT07120932Updated Aug 14, 2026

Effects of Emotional Freedom Techniques on Pain, Cardiac Anxiety, and Sleep Quality in Coronary Artery Bypass Grafting

An interventional study of Effects of Emotional Freedom Techniques (EFT) in Coronary Artery Bypass Graft (CABG) and Effects of Emotional Freedom Techniques (EFT), sponsored by Hatice Balcı. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-14.

Sponsored by Hatice Balcı · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
66
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study 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.

02

Conditions studied

  • Coronary Artery Bypass Graft (CABG)
  • Effects of Emotional Freedom Techniques (EFT)

Keywords

  • Coronary Artery Bypass Graft Surgery
  • Effects of Emotional Freedom Techniques (EFT)
  • Pain Management
  • Anxiety
  • Sleep
03

In context

Agnosia

1,190 studies on the registry are indexed under Agnosia; 508 are open to participants now.

This study's enrollment of 66 is below the median of 78 across 1,024 interventional studies indexed under Agnosia.

Browse Agnosia studies →

Lead sponsor

This is the only study on the registry with Hatice Balcı as lead sponsor.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria: 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.

Exclusion Criteria:

  • 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.
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
66 participants (actual)

Study arms

  • Experimental
    Emotional Freedom Techniques (EFT)

    Effects of Emotional Freedom Techniques (EFT)

    Behavioral: Effects of Emotional Freedom Techniques (EFT)

  • No intervention
    Control arm

    Standard care will continue without intervention.

Interventions

  • BehavioralEffects of Emotional Freedom Techniques (EFT)

    Effects of Emotional Freedom Techniques (EFT)

06

What researchers measure

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).

    Time frame: 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 effect of EFT on the patient's cardiac anxiety level will be measured. The Effect of Emotional Freedom Techniques (EFT) on Cardiac Anxiety Levels in Patients Undergoing Coronary Artery Bypass Graft Surgery. The measurement tool is a Cardiac Anxiety Scale.

    Time frame: 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 effect of EFT on the patient's sleep quality will be measured. The Effect of Emotional Freedom Techniques (EFT) on Sleep Quality in Patients Undergoing Coronary Artery Bypass Graft Surgery. The measurement tool is a Richard Campbell Sleep Scale.

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

07

Study locations

1 site
  • KTO Karatay University
    Konya, Karatay 42020, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No — 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.

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 Aug 14, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07120932
Lead sponsor
Hatice Balcı
Responsible party
Hatice Balcı (PhD, KTO Karatay University) — Sponsor-investigator
First posted
Aug 13, 2025
Start date
Jun 30, 2025
Primary completion
Jan 15, 2026
Completion
Apr 10, 2026
Last update
Aug 14, 2026

Oversight

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

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This study is completed, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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