ClinicalTrials.Veeva

Menu

Emotional Freedom Technique During Pregnancy

K

KTO Karatay University

Status

Not yet enrolling

Conditions

Birth Memory
Fear of Birth

Treatments

Other: EFT intervention

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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 June 2025 and December 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.

Enrollment

70 estimated patients

Sex

Female

Ages

18 to 49 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Primary education level or higher
  • Able to speak, understand and write Turkish,
  • 18 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.

Exclusion criteria

  • 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.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

70 participants in 2 patient groups

EFT intervention
Experimental group
Description:
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.
Treatment:
Other: EFT intervention
Control grup
No Intervention group
Description:
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

Trial contacts and locations

1

Loading...

Central trial contact

Merve Yazar, Lecturer, PhD (c)

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems