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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06429254
Other study ID # 01/05
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 24, 2024
Est. completion date October 1, 2024

Study information

Verified date May 2024
Source Karabuk University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 64
Est. completion date October 1, 2024
Est. primary completion date September 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 49 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Other:
Experimental group
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.

Locations

Country Name City State
Turkey Trakya University Edirne
Turkey Trakya University Edirne

Sponsors (1)

Lead Sponsor Collaborator
Karabuk University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Examining the Effect of Emotional Freedom Technique on Pelvic Pain In Endometriosis Emotional Freedom Techniques 1 time per month up to 2 months, Pain will be assessed using the VAS (Visual Analogue Scale). A high score on the scale indicates high pain.
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