The Effect of Emotional Freedom Technique and Music Recital on Pain and Anxiety Experienced During Intrauterine Device Application
Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
The purpose of this study is to determine the effect of emotional freedom technique and music, which are effective in relieving pain and anxiety, on the pain and anxiety that occur during intrauterine device application.
Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 49
Healthy Volunteers: t
View:
• Voluntarily agreeing to participate in the research
• Being between the ages of 18-49
Locations
Other Locations
Turkey
Şırnak State Hospital
RECRUITING
Şırnak
Contact Information
Primary
Ceylan l GÜZEL İNAL, Lecturer
cylngzl@hotmail.com
+905432588644
Backup
Sermin TİMUR TAŞHAN, Prof. Dr.
setimur@gmail.com
+905066047909
Time Frame
Start Date: 2023-07-01
Estimated Completion Date: 2024-04
Participants
Target number of participants: 168
Treatments
Experimental: Emotional freedom technique group
Pre-test data will be collected after women are informed about the emotional freedom technique. After the pre-test data is collected, the emotional liberation technique will be applied to the women. After the emotional liberation technique session is completed, the intrauterine device (IUD) will be applied. Post-test data will be collected within 10 minutes after IUD application is completed.
Experimental: Music group
Women in the music group will be informed about the procedure steps before intrauterine device (IUD) application and pre-test data will be collected. After the pre-test data is collected, the music list prepared by the women and researchers will be shown and the women will be asked to choose a piece. Women who do not want to listen to any music on this list will be allowed to listen to the music they prefer. The music concert will be performed with headphones, and women will be asked to listen to the music until the IUD application process is completed. Post-test data will be collected within 10 minutes after IUD application.
Other: Control group
No intervention will be applied to women in the control group.
Related Therapeutic Areas
Sponsors
Leads: Inonu University
Collaborators: The Scientific and Technological Research Council of Turkey