The Effect of Emotional Freedom Techniques on Pelvic Pain

November 25, 2025 updated by: Ayse Cuvadar, Karabuk University

Effect of Emotional Freedom Techniques on Pelvic Pain and Quality of Life in Women With Endometriosis: A Randomized Controlled Study

Pelvic pain caused by endometriosis is a common symptom and reduces women's quality of life.

EFT is a method that can be preferred in pelvic pain due to its ease of use and low cost.

Raising women's awareness for EFT

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Pelvic pain caused by endometriosis is a common symptom and reduces women's quality of life. EFT has become widely used in medical and psychological treatment settings in recent years.It is also used as a self-help technique by millions of people every year.EFT is a method that can be preferred in pelvic pain due to its ease of use and low cost.

Study Type

Interventional

Enrollment (Actual)

64

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Edirne
      • Edirne, Edirne, Turkey (Türkiye), 22100
        • Trakya University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  1. Being diagnosed with endometriosis
  2. Experiencing pelvic pain
  3. Being between the ages of 18-49
  4. Those whose symptom complaints are 5 or above on the visual analogue scale

Exclusion Criteria:

  1. Patients with known systemic diseases (e.g. hypertension, diabetes, coronary, kidney and liver diseases);
  2. Patients with known malignancy;
  3. Women in menopause;
  4. Having any obstacle to communication

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Emotional Freedom Techniques group

First, the Personal Information Form, Visual Analogue Scale, and Quality of Life Scale will be administered as pre-tests to the EFT group. A high score obtained from the quality of life scale indicates a high quality of life.

After the pre-tests, the first EFT session will be conducted. A second EFT session will take place 30 days later, followed by post-tests. During this period, affirmations will be provided as needed based on individual difficulties, perspectives, support systems, past traumas, and emotional blockages experienced by the woman. Each session is planned to last approximately 45 minutes to 1 hour.

Procedure: Administering pre-tests followed by the first EFT session. Procedure: After 30 days, conducting post-tests followed by the second EFT session.

Procedure: After another 30 days, only post-tests will be conducted.

Life Scale will be administered as pre-tests to the EFT group. After the pre-tests, the first EFT session will be conducted. A second EFT session will take place 30 days later, followed by post-tests. During this period, affirmations will be provided as needed based on individual difficulties, perspectives, support systems, past traumas, and emotional blockages experienced by the woman. Each session is planned to last approximately 45 minutes to 1 hour.
Other Names:
  • EFT group
No Intervention: Control group

After obtaining consent from the women included in the group, pre-tests will be conducted followed by breathing exercises. A program will be tailored according to the suitability of the women. Once an appropriate environment is provided for meeting with the women, information about the study will be provided. Pain coping methods will be explained, and breathing exercises will be taught. The exercises will commence when the woman feels ready. The breathing exercises typically last around 15-20 minutes.

With a plan for a total of 8 breathing exercises to be conducted over four weeks, consisting of 2 sessions per week, they will be scheduled to coincide with the EFT group, with sessions held every 5 days.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Examining the Effect of Emotional Freedom Technique on Pelvic Pain in Endometriosis
Time Frame: 2 months; participants will receive 2 EFT sessions, one session per month. Pain and quality of life will be assessed at baseline and after 2 months.

Primary Outcome Measures: Pain measured using the Visual Analog Scale (VAS); higher scores indicate greater pain.

Secondary Outcome Measures: Quality of life measured using the SF-36; higher scores indicate better quality of life.

2 months; participants will receive 2 EFT sessions, one session per month. Pain and quality of life will be assessed at baseline and after 2 months.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 24, 2024

Primary Completion (Actual)

October 27, 2024

Study Completion (Actual)

December 11, 2024

Study Registration Dates

First Submitted

April 27, 2024

First Submitted That Met QC Criteria

May 20, 2024

First Posted (Actual)

May 24, 2024

Study Record Updates

Last Update Posted (Estimated)

December 3, 2025

Last Update Submitted That Met QC Criteria

November 25, 2025

Last Verified

November 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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