The Effect of Emotional Freedom Technique on Parents' Anxiety Level: Newborn Hearing Screening
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAbant Izzet Baysal University
About this trial
Newborn hearing screening (NHS) is a standard procedure that often triggers acute anxiety in parents. While Emotional Freedom Technique (EFT) has demonstrated efficacy in reducing psychological distress across various clinical settings, its specific application to parental anxiety during the neonatal screening period remains under-researched. This study addresses this gap by investigating the impact of a targeted EFT intervention on anxiety levels in mothers awaiting their newborns' first hearing tests.
The primary objective is to determine if a brief, 15-minute EFT session reduces maternal anxiety more effectively than a standard waiting period. Participants are randomly assigned to either an intervention group, where they perform a structured acupoint tapping sequence, or a control group that receives no active intervention. Anxiety is assessed using validated scales immediately before and after the 15-minute period to capture acute changes in distress. The researchers hypothesize that applying EFT regarding the procedure will significantly reduce parental anxiety levels compared to the non-intervention group.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Parents of neonates who are undergoing the newborn hearing screening (NHS) for the first time.
Ability to communicate effectively in the native language without language barriers.
No prior experience or training in applying the Emotional Freedom Technique (EFT).
Voluntary agreement to participate in the study and completion of the informed consent form.
Disqualifiers
Known history of diagnosed psychiatric disorders or epilepsy.
Situations where the neonate is crying or being breastfed immediately prior to the intervention or during the assessment.
The scheduled hearing screening procedure is initiated before the 30-35-minute study protocol is completed.
Occurrence of any acute situational triggers or environmental distractions that may interfere with the stability of anxiety measurements.
Trial design
Design model
Parallel
Treatments tested in this trial
Emotional Freedom Technique
Behavioral15-minute guided acupoint tapping session
No intervention
Other intervention15-minute waiting period without active guidance
Treatment groups
70 Participants
are divided into 2 treatment groupsGroup A: Emotional Freedom Technique GroupExperimental treatment 1 intervention
Group B: Control GroupOther 1 intervention
Trial outcomes
Primary outcomes
1
State Anxiety Inventory (STAI-S) Score
The STAI-S measures the current state of anxiety. Scores range from 20 to 80, where higher scores indicate greater levels of anxiety.
Time frame
Baseline (Pre-test) and 15 minutes after the baseline (Post-test)Secondary outcomes
1
Subjective Units of Distress Scale (SUDS)
A self-assessment scale for distress/anxiety. Scores range from 0 (no distress) to 10 (extreme distress).
Time frame
Baseline (Pre-test) and 15 minutes after the baseline (Post-test).2
State-Trait Anxiety Inventory - Trait (STAI-T) Score
The STAI-T is a self-report scale used to measure an individual's general tendency to experience anxiety. The scale consists of 20 items, with scores ranging from 20 to 80. Higher scores reflect a higher level of trait anxiety.
Time frame
Baseline (Pre-test) and 15 minutes after the baseline (Post-test).Sponsors and contacts
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Source ClinicalTrials.gov