Emotional Freedom Technique During Pregnancy

NCT07000552 | Completed DMC

• 1 other identifier: MerveU
• Study Type: interventional
• Target: 68
• Locations: 1 country
• Sites: 1

Brief Summary

Emotional Freedom Technique (EFT), also known as "Tapping Therapy" and "Needleless Acupuncture", is a new and emerging complementary and energy-based therapy. It is a psychophysiological intervention combining cognitive behavioural therapy, exposure therapy and physical stimulation using acupressure points. This research will be conducted to evaluate the effect of emotional liberation technique applied to primigravidas on fear of childbirth, birth memory and postpartum feelings of safety. The research will be conducted between January 2025 and October 2025 in Konya Necmettin Erbakan University Faculty of Medicine Hospital, Department of Obstetrics and Gynaecology, Pregnant Outpatient Clinic with primiparous women planning vaginal delivery. This research is planned to be conducted with two groups, EFT intervention and control group. The population of the study consisted of pregnant women who applied to the pregnancy outpatient clinic of a university hospital located in the city centre of Konya province and were evaluated for eligibility.

Conditions

Fear of Birth; Birth Memory; Postpartum Sense of Security

Keywords

emotional freedom technique

Outcome Measures

Primary Outcomes (2)

• EFT Intervention

  Women with a gestational age of 32 and above will be administered the Subjective Experience Unit scale before and after the intervention. The Subjective Experience Unit scale was developed by Hartmann with the "Events Psychology" approach in order to measure the energy flow in the energy body. This scale is used to determine the emotional intensity of the person at the beginning and at the end of the EFT session. In this scale, scoring is made between -10 and +10. -10 is the greatest pain, disappointment, fear, stress, sadness or discomfort imaginable, while +10 is the highest level of joy, happiness or feeling great. The final tests will be administered in the postnatal period. In the postnatal period, Wijma Birth Anticipation/Experience Scale, Birth Memory and Recall Scale, Postnatal Feelings of Security Scale and Postnatal Interview Form were completed.

  4 weeks

• Control grup

  Pregnant women in the control group will be called once a week and asked to score the SUE scale and recorded, and 1 hour later, they will be asked to score the SUE scale again without any intervention. Final tests will be administered in the postnatal period.

  4 week

Study Arms (2)

EFT intervention

EXPERIMENTAL

The implementation will be carried out in accordance with EFT implementation protocols. In this context, it will be completed with 4 interviews, once a week for pregnant women. i Each EFT session will last 15 minutes.

Other: EFT intervention

Control grup

NO INTERVENTION

There will be no intervention. Women in the intervention groups will be followed up for 4 weeks and will receive standardised care. The final test will be administered in the postnatal period

Interventions

EFT intervention OTHER

The intervention groups will be followed up for 4 weeks and 4 EFT therapies will be applied, one session per week.

EFT intervention

Eligibility Criteria

• Age: 18 Years - 49 Years
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Primary education level or higher
• Able to speak, understand and write Turkish,
• years of age or older,
• Residing in Konya province,
• No disability for vaginal delivery,
• Primigravida,
• Anxiety level of 1 or higher when measured with the subjective discomfort unit scale,
• Pregnant women who are at 32 weeks of gestation or above according to the last menstrual date or according to calculations made with USG data for pregnant women who do not know the last menstrual date.

You may not qualify if:

• Pregnant individuals with high-risk pregnancies,
• Those who have undergone infertility treatment,
• Those with any fetal health problems,
• Those with physical or mental illnesses,
• Those with a cesarean section indication or who plan to deliver via cesarean section,
• Those with chronic and/or psychiatric health issues and those who have participated in any childbirth preparation education were excluded from the study.

Sponsors & Collaborators

• KTO Karatay University: lead
• EMEL EGE: collaborator

Study Sites (1)

KTO Karatay University

Konya, Konya, 42020, Turkey (Türkiye)

Location

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: OUTCOMES ASSESSOR
• Purpose: SUPPORTIVE CARE
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Lecturer, PhD (c)

Study Record Dates

• First Submitted: May 24, 2025
• First Posted: June 3, 2025
• Study Start: January 15, 2025
• Primary Completion: October 15, 2025
• Study Completion: November 15, 2025
• Last Updated: December 17, 2025

Record last verified: 2025-12

Data Sharing

• IPD Sharing: Will not share

Locations

TU (1)