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Clinical Trials/NCT06296927
NCT06296927
Completed
Not Applicable

The Effect of the Emotional Freedom Technique Applied During Mammography Screening on Perceived Pain, Situational Anxiety and Satisfaction Levels

Saglik Bilimleri Universitesi1 site in 1 country94 target enrollmentNovember 7, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Mammography Screening
Sponsor
Saglik Bilimleri Universitesi
Enrollment
94
Locations
1
Primary Endpoint
Anxiety
Status
Completed
Last Updated
11 months ago

Overview

Brief Summary

This study was planned to determine the effect of Emotional Freedom Technique on perceived pain level, situational anxietyl and satisfaction level during mammography screening.

Detailed Description

The randomized controlled and experimental study will be conducted with 94 women who applied to the Cancer Early Diagnosis, Screening and Education Center for mammography screening. The women in the experimental group (n=47) will be applied the Emotional Freedom Technique before mammography screening and the women in the control group (n=47) will be given routine mammography screening. The Sociodemographic Information Form, Visual Analog, Situational Anxiety Inventory, blood pressure monitor, thermometer and saturation device will be used to collect the data.

Registry
clinicaltrials.gov
Start Date
November 7, 2024
End Date
March 30, 2025
Last Updated
11 months ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sümeyye Köse

Principal Investigator Midwife

Saglik Bilimleri Universitesi

Eligibility Criteria

Inclusion Criteria

  • Having a first mammography screening
  • Knowing how to read and write,
  • Having entered menopause (at least 1 year has passed since the last menstruation)

Exclusion Criteria

  • Having any cognitive or hearing problems,
  • Having used painkillers before the procedure,
  • Having no chronic diseases (cardiovascular, respiratory tract),
  • Having a diagnosed mental illness (schizophrenia, bipolar disorder),
  • Having epilepsy (as it is a contraindication for EFT applications),

Outcomes

Primary Outcomes

Anxiety

Time Frame: 20 minute

Data will be collected using the State Anxiety Inventory. The answer options collected in four classes on the State Anxiety Inventory scale are: (1) Not at all, (2) A little, (3) A lot and (4) Completely; The options on the trait anxiety scale are (1) Rarel, (2) Sometimes, (3) A lot of the time, and (4) Almost always. The higher the score obtained from the scales, the higher the person's anxiety is. The total score obtained from the scale varies between 20-80, and 20-39 indicates a mild anxiety level, 40-59 indicates a medium anxiety level, 60-79 indicates a high anxiety level, and 80 points indicates a panic anxiety level.

Pain Level

Time Frame: 10 minute

Data will be collected using the Visual Analogue Scale. Pain can be given a score between 0 and 10 on the scale.The higher the scale score, the greater the pain.

Secondary Outcomes

  • Satisfaction Level(10 minutes)
  • Blood Pressure(5 minutes)
  • Thermometer(5 minutes)
  • Saturation(5 minutes)

Study Sites (1)

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