- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06129279
Effect of Emotional Freedom Technique on Symptoms in Dysmenorrhea
Examining the Effect of Emotional Freedom Technique on Quality of Life and Symptoms in Dysmenorrhea
- Reducing symptoms with EFT in young women suffering from dysmenorrhea
- Improving the quality of life of young women suffering from dysmenorrhea
- Raising women's awareness for EFT
- Reducing healthcare costs for dysmenorrhea
Study Overview
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Karabuk, Turkey, 78050
- Karabuk University
-
-
Karabuk
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Karabük, Karabuk, Turkey, 78050
- Karabuk University
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
• Being a female student at Karabük University Faculty of Health Sciences
- Being between the ages of 18-25
- Voluntarily agrees to participate in the study,
- T.R. to be a citizen,
- Not having any chronic disease,
- Those whose symptom complaints are 5 or above according to the VAS scale
Exclusion Criteria:
• Leaving the study at any time,
- Having any diagnosed psychiatric disorder.
- Not having secondary dysmenorrhea pathology
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: İntervention (EFT) group
In order to determine the students who meet our study criteria, PİF, DDF, VAS, MSS and Short Form 36 will be applied for the pre-test to female students studying in the relevant departments of KBÜ SBF. To EFT Group; After the first tests are done, the 1st EFT session will be held, the 2nd EFT session will be held 30 days later, and the final tests will be done 30 days later. During this period, affirmations will be given depending on the need. Each session is planned to last an average of 45 minutes - 1 hour, and duration and affirmations will be arranged according to the woman's individual difficulties, perspective, support systems, past traumas and emotional blockages. 4th Procedure: Preliminary tests will be carried out and then the 1st EFT session will be held. 5. Procedure: After 30 days, the first final tests will be performed and then the second EFT session will be held. Procedure 6: After 30 days, only the 2nd final tests will be performed. |
Preliminary tests will be carried out and then the 1st EFT session will be held. After 30 days, the first final tests will be performed and then the second EFT session will be held. After 30 days, only the 2nd final tests will be performed. |
|
No Intervention: Control group
In order to determine the students who meet our study criteria, PİF, DDF, VAS, MSS and Short Form 36 will be applied for the pre-test to female students studying in the relevant departments of KBÜ SBF. Students in the control group will receive routine counseling regarding primary dysmenorrhea, and no extra intervention or practice will be performed. Procedure 1: Preliminary tests will be conducted and then general training for dysmenorrhea will be conducted. 2nd Process: 30 days later, the questions of the students who will take the 1st post-test will be answered. 3rd Procedure: After 30 days, the second final tests will be performed. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Examining the Effect of Emotional Freedom Technique on Quality of Life and Symptoms in Dysmenorrhea
Time Frame: Preliminary tests will be carried out and then the 1st EFT session will be held. After 30 days, the first final tests will be performed and then the second EFT session will be held. After 30 days, only the 2nd final tests will be performed.
|
Emotional Freedom Technique
|
Preliminary tests will be carried out and then the 1st EFT session will be held. After 30 days, the first final tests will be performed and then the second EFT session will be held. After 30 days, only the 2nd final tests will be performed.
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- E-77192459-050.99-232650
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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